Indian Patents
Title of Invention

A SUBSTITUTED PYRAZOLES COMPOUND OF FORMULA (1)
Abstract Substituted pyrazoles, methods of manufacturing them, compositions containing them, and methods of using them to treat, for example, autoimmune diseases mediated by cathepsin S are described.
Full Text SUBSTITUTED PYRAZOLES
Field of the Invention
This invention relates to a series of substituted pyrazoles,
pharmaceutical compositions containing these compounds, and intermediates
used in their manufacture, and methods of using them.
Background of the Invention
Cathepsin S (EC 3.4.22.27) is a cysteine protease of the papain family
found primarily in lysosomes (Bromme, D.; McGrath, M. E. High Level
Expression and Crystallization of Recombinant Human Cathepsin S. Protein
Science 1996, 5, 789-791).
The role of cathepsin S in the immune response is anticipated by its
tissue distribution: cathepsin S is found primarily in lymphatic tissues, lymph
nodes, the spleen, B lymphocytes, and macrophages (Kirschke, H. Chapter
211. Cathepsin S. In Handbook of Proteolytic Enzymes. Barrett, A. J.;
Rawlings, N. D.; Woessner, J. F., Eds. San Diego: Academic Press, 1998. pp.
621-624.). Cathepsin S inhibitors have been shown in animal models to
modulate antigen presentation and are effective in an animal model of asthma
(Riese, R. J.; Mitchell. R. N.; Villadangos, J. A.; Shi, G.-P.; Palmer, J. T.; Karp,
E. R.; De Sanctis, G. T.; Ploegh, H. L.; Chapman, H. A. Cathepsin S Activity
Regulates Antigen Presentation and Immunity. J. Clin. Invest. 1998, 101,
2351-2363 and Shi, G.-P.; Villadangos, J. A.; Dranoff, G.; Small, C; Gu, L.;
Haley, K. J.; Riese, R.; Ploegh, H. L.; Chapman, H. A. Cathepsin S Required
for Normal MHC Class II Peptide Loading and Germinal Center Development.
Immunity 1999, 10, 197-206.).
Mice in which the gene encoding cathepsin S has been knocked out are
less susceptible to collagen-induced arthritis and their immune systems have

an impaired ability to respond to antigens (Nakagawa, T. Y.; Brissette, W. H.;
Lira, P. D.; Griffiths, R. J.; Petrushova, N.; Stock, J.; McNeish, J. D.; Eastman,
S. E.; Howard, E. D.; Clarke, S. R. M.; Rosloniec, E. F.; Elliott, E. A.;
Rudensky, A. Y. Impaired Invariant Chain Degradation and Antigen
Presentation and Diminished Collagen-Induced Arthritis in Cathepsin S Null
Mice. Immunity 1999, 10, 207-217).
These data demonstrate that compounds that inhibit the proteolytic
activity of human cathepsin S should find utility in the treatment of chronic
autoimmune diseases including, but not limited to, lupus, rheumatoid arthritis,
and asthma; and have potential utility in modulating the immune response to
tissue transplantation.
There are a number of cathepsin S inhibitors reported in the literature.
The most important patents are listed below.
Certain dipeptidyl nitriles are claimed by Novartis as catheDsin S
inhibitors in: Altmann, et. al. WO-99/24460.
Dipeptidyl vinyl sulfones are claimed by Arris (now Axys) as cysteine
protease (including cathepsin S) inhibitors in: Palmer, et. al. US-5976858.
Certain peptidyl sulfonamides are claimed by Arris/Axys as cysteine
protease (including cathepsin S) inhibitors in: Palmer, et. al. US-5776718
(assigned to Arris, now Axys) & Klaus, et. al. US-6030946 (assigned to Axys).
Compounds somewhat similar to those of the present invention are
described in the following references.
Winters, et. al. (Winters, G.; Sala, A.; Barone, D.; Baldoli, E. J. Med.
Chem. 1985, 28, 934-940; Singh, P.; Sharma, R. C. Quant. Struct.-Act Relat.
1990, 9, 29-32; Winters, G.; Sala, A.; Barone, D. in US-4500525 (1985)) have
described bicyclic pyrazoles of the type shown below. R never contains a

heterocyclic ring and no protease inhibitor activity is ascribed to these
molecules; they are described as a1-adrenergic receptor modulators.

Shutske, et. al. claim the bicylic pyrazoles below. The pyridine ring is
aromatic in their system (Shutske, G. M.; Kapples, K. J.; Tomer, J. D. US-
5264576 (1993)). Although reference is made to R being a linker to a
heterocycle, the claims specify only R = hydrogen. The compounds are
referred to as serotonin reuptake inhibitors.

The compound 2-[4-[4-(3-methyl-5-phenyl-1 H-pyrazol-1-yl)butyl]-1-
piperazinyl]-pyrimidine is known from EP-382637, which describes pyrimidines
having anxiolytic properties. This compound and analogs are further described
in EP-502786 as cardiovascular and central nervous system agents.
Pharmaceutical formulations with such compounds are disclosed in EP-655248
for use in the treatment of gastric secreation and as anti-ulcer agents. WO-
9721439 describes medicaments with such compounds for treating obsessive-
compulsive disorders, sleep apnea, sexual dysfunctions, emesis and motion
sickness.

The compounds 5-methyl-3-phenyl-1-[4-(4-phenyl-1-piperazinyl)butyl]-
1H-indazole and 5-bromo-3-(2-chlorophenyl)-1-[4-(4-phenyl-1-
piperazinyl)butyl]-1H-indazole, in particular the hydrochloride salts thereof, are
known from WO-9853940 and CA 122:314528, where these and similar
compounds are described as kinase inhibitors in the former reference and
possessing affinity for benzodlazepine receptors in the latter reference.

The present invention concerns compounds which can be represented by
formula (I):

wherein:
the dashed line adjacent C-R6 is absent or an sp2 bond;
Y is nitrogen or R20C;
Z is nitrogen or R21C;
T is nitrogen or R2C;
S is nitrogen or R3C;
provided between 0 and 3 of S, T, Y, and Z are nitrogen; and further
provided that one of S, T, Y, and Z can be =N+-O- where the remaining
three are not nitrogen;
R20 is selected from hydrogen, halogen, C1-5 alkoxy, hydroxy, C1-5 alkyl,
cyano, nitro, C1-5haloalkyl, RoRpN, RoRpNC=O, C2-6acyl, 4-7 membered
heterocyclyl, (4-7 membered heterocyclyl)- C1-5 alkylene, phenyl,
(phenyl)C1-5alkylene, R14OC=O, R14S, R14SO,and R14SO2;
R21 is selected from hydrogen, halogen, C1-5alkoxy, hydroxy, C1-5 alkyl,
cyano, nitro, C1-5haloalkyl, RcRdN, RcRdNC=O, C2-8acyl, 4-7 membered

heterocyclyl, (4-7 membered heterocyclyl)-C 1-5 alkylene, phenyl,
(phenyl)C 1-5 alkyiene. R15OC=O, R15S, R16SO,and R15SO2;
R2 is selected from hydrogen, halogen, C1-5alkoxy, hydroxy, C1-5 alkyl,
cyano, nitro, C1-5hatoalkyl, ReRfN, ReRfNC=O, C2-8acyl, 4-7 membered
heterocyclyl, (4-7 membered heterocyclyl)-C1-5 alkylene, phenyl,
(phenyl)C 1-5 alkylene, R18OC=O, R16S, R16SO and R16SO2
R3 is selected from hydrogen, halogen, C1-5alkoxy, hydroxy, C1-5 alkyl,
cyano, nitro, C1-5haloalkyl, RgRhN, C2-8acyl, 4-7 membered heterocyclyl,
(4-7 membered heterocyclyl)- C 1-5 alkylene, phenyl, (phenyl)C 1-6
alkyiene, R17OC=O, RmRnNC=O, RmRnNSO2, R17S, R17SO and R17SO2;
Rs and R6 are independently selected from hydrogen and C1-5 alkyl;
R7 and R8 independently are hydrogen, C1-5 alkyl, C1-5 alkenyl, C1-5 alkoxy, C1-5
alkylthio, halogen, or 4-7 membered carbocydyl or heterocyclyl;
alternatively, R7 and R8 can be taken together to form an optionally
substituted 5- to 7- membered carbocyclic or he ocyclic ring, which
ring may be unsaturated or aromatic; said ring being optionally
substituted with between 1 and 3 substituents independently selected
from halo, hydroxy, cyano, nitro, amino, Rt RtO-, RtS-, RtO(C 1-5
alkylene)-, RtO(C=O)-, Rt(C=O)-, Rt(C=S)-, Rt(C=O)O-, RtO(C=O)(C=O)-,
RtSO2, NHRU(C=NH)-, NHRUSO2-, and NHRU(C=O)-;
Rt is C 1-6 alkyl, phenyl, benzyl, phenethyl, or C 2-5 heterocyclyl, (C 1-5
heterocydyl)C 1-6 alkylene, NH2, mono- or di(C 1-6 alkyl)N-, or R49OR50-,
wherein R49 is H, C 1-5 alkyl, C 2-5 alkenyl, phenyl, benzyl, phenethyl, C 1-5
heterocyclyl, or (C 1-5 heterocydyl)C 14 alkyiene and R50 is C 1-5 alkyiene,
phenylene, or divalent C1-5 heterocydyl; and
Ru can be H in addition to the values for Rt;
Rc is hydrogen, C1-5 alkyl, phenyl, C 2-5 heterocyclyl, C 2-8 acyl, aroyl,
R10OC=O-, RiRJNC=O, R10SO-, R10SO2-, and RiRJNSO2;
Re is hydrogen, C1-5 alkyl, phenyl, C2-5 heterocydyl, C 2-8 acyl, aroyl,
R40OC=O, R43R44NC=O, R40SO, R40SO2, and R43R44NSO2;
Rm is hydrogen, C1-5 alkyl, phenyl, C 2-5 heterocydyl, C 2-8 acyl, aroyl,
R41OC=O, R45R46NC=O, R41SO, R41SO2, and R45R46NSO2;

R° is hydrogen, C1-5 alkyl, phenyl, C 2-5 heterocyclyl, C 2-8 acyl, aroyl,
R42OC=O, R47R48NC=O, R42SO, R42SO2, and R47R48NSO2.
each of Rd, Rf, Rn, and Rp is independently selected from hydrogen, C1-5 alkyl,
phenyl, and C 2-5 heterocyclyl; in addition, Rc and Rd, Re and Rf, Rm and
Rn, or R° and Rp, independently, can be taken together to form an
optionally substituted 4- to 7-membered heterocyclic ring, which ring
may be saturated, unsaturated or aromatic;
each of R9, R10, R11, R14, R15, R16, R17, R40, R41, and R42 is independently C1-5
alkyl, phenyl, or C 2-5 heterocyclyl;
each of Ri and Rj, Rk and Rl, R43 and R44, R45 and R46, R47 and R48 are
independently hydrogen, C1-5 alkyl, C3-5 alkenyl, phenyl, or C 2-5
heterocyclyl; in addition, Rj and Rj, and Rk and Rl, R48 and R44, R45 and
R46, and R47 and R48, independently, can be taken together to form an
optionally substituted 4- to 7-membered heterocyclic ring, which ring
may be saturated, unsaturated or aromatic;
Rs is hydrogen, C1-5 alkyl, phenyl, or C 2-5 heterocyclyl, C 2-8 acyl, aroyl,
R9OC=O, R18R19NC=O, R9SO, R9SO2, or R18R19NSO2;
Rh is hydrogen, C1-5 alkyl, phenyl, or C 2-5 heterocyclyl;
alternatively, R° and Rh can be taken together to form an optionally
substituted 4- to 7- membered heterocydic ring, which ring may be
saturated, unsaturated or aromatic;
R18 and R19 independently are hydrogen, C1-5 alkyl, phenyl, or C 2-5 heterocyclyl;
alternatively, R18 and R19 can be taken together to form an optionally
substituted 4- to 7- membered heterocydic ring, which ring maybe
saturated, unsaturated or aromatic;
n is 0, 1 or 2;
G is C3-6 alkenediyl or C3-6 alkanediyl, optionally substituted with hydroxy,
halogen, C1-5 alkyl, C1-5alkoxy, oxo, hydroximino, CO2Rk NRkRl, (L)-C 1-4
alkylene-, RkRlNCO2, [(L)-C 1-5 alkylene]amino, N3, or (L)-C14 alkoxy;
L is amino, mono- or di-C1-5alkylamino, pyrrolidinyl, morpholinyl,
piperidinyl, homopiperidinyl, or piperazinyl, wherein available ring
nitrogens can be optionally substituted with C1-5 alkyl, benzyl, C2-5acyl, C
1-5 alkylsulfonyl, or C1-5alkoxycarbonyl;

Ar represents a monocyclic or bicyclic aryt or heteroaryl ring, optionally
substituted with between 1 and 3 substituents independently selected
from halogen, C1-5alkoxy, C1-5 alkyl, C2-5alkenyl, cyano, azido, nitro,
R22R23N, R22S, R22SO, R22SO2, R22OC=O, R22R23NC=O, C1-5 haloalkyl, C1-
5haloalkoxy, C1-5hatoalkylthio, and C1-5 alkylthio;
R22 is hydrogen, C1-5 alkyl, C3-5alkenyl, phenyl, benzyl, C 2-5 heterocyclyl, C 2-8
acyl, aroyl, R11OC=O, R24R25NC=O, R11S, R11SO, R11SO2, or
R23 is hydrogen, C1-5 alkyl, phenyl, benzyl, or C 2-5 heterocyclyl;
alternatively, R22 and R23 can be taken together to form an optionally
substituted 4- to 7-membered heterocyclic ring, which ring may be
saturated, unsaturated or aromatic;
R24 and R25 are independently hydrogen, C1-5 alkyl, phenyl, benzyl, or C 1-5
heteroaryl;
alternatively, R24 and R25 can be taken together to form an optionally
substituted 4- to 7- membered carbocyclic or heterocyclic ring, which
ring may be saturated, unsaturated or aromatic;
R32 is hydrogen, C1-5 alkyl, cyano, C1-5 hydroxyalkyl, C2-8, acyl, -(C=O)NRvRx,
CHO, or C1-6 alkoxycarbonyl, wherein each of Rv and Rx is independently
selected from H , C1-5 alkyl, C1-5 hydroxyalkyl, C1-5 heterocyclyl, (C1-5
heterocyclyl) C1-5 alkylene, C1-5 aminoalkylene, C3-8 acyloxy, CHO, C1-6
alkoxycarbonyl, and cyano;
Q is NR33, S, or O;
R33 represents hydrogen, C1-5 alkyl, phenyl, benzyl, phenethyl, C2-5
heterocyclyl, (C2-5 heterocyclyl)C 1-5 alkylene, C2-8 acyl, aroyl, R35OC=O,
R36R37NC=O R35SO, R35S, R35SO2 and R36R37NSO2;
R35 is selected from hydrogen, C1-5 alkyl, phenyl, benzyl, phenethyl, and C 2-5
heteroaryl;
R36 and R37 are each independently selected from hydrogen, C1-5 alkyl, phenyl,
or C 2-5 heteroaryl;
alternatively, R36 and R37 can be taken together to form an optionally
substituted 4- to 7-membered ring heterocyclic ring, which ring may be
saturated, unsaturated or aromatic;

wherein each of the above hydrocarbyl or heterocarbyi groups, unless
otherwise indicated, and in addition to any specified substituents, is
optionally and independently substituted with between 1 and 3
substituents selected from methyl, halo methyl, hydroxymethyl, halo,
hydroxy, amlno, nrtro, cyano, C 1-5 alkyl, C 1-5 alkoxy, -COOH, C 2-6 acyl,
[di(C 1-4 alkyl)amino]C 2-5 alkylene, [di(C 1-4 alkyl)amino] C 2-5 alkyl-NH-
CO-, and C 1-5 haloalkoxy;
or a pharmaceutically acceptable salt, amide, or ester thereof, or a
stereoisomeric form thereof.
The disclosed compounds are high-affinity inhibitors of the proteoiytic
activity of human cathepsin S. For use in medicine, the preparation of
pharmaceutically acceptable salts of compounds of formula (I) may be
desirable.
Certain compounds of the present invention may have one stareogenic
atom and may exist as two enantiomers. Certain compounds of the present
invention may have two or more stereogenic atoms and may further exist as
diastereomers. It is to be understood by those skilled in the art that all such
stereoisomers and mixtures thereof in any proportion are encompassed within
the scope of the present invention.
Another aspect of the invention provides pharmaceutical compositions
comprising a compound of formula (I) and a pharmaceutically acceptable
carrier. A further embodiment of the invention is a process for making a
pharmaceutical composition comprising mixing a disclosed compound as
described above, with a suitable pharmaceutically acceptable carrier.
The invention also contemplates pharmaceutical compositions
comprising more than one compound of formula (I) and compositions

comprising a compound of formula (I) and another pharmaceutically active
agent.
The invention features a method of treating disorders or conditions
mediated by the cathepsin S enzyme, in a subject in need thereof, comprising
administering to the subject a therapeutically effective amount of any of the
compounds or pharmaceutical compositions described above. If more than
one active agent is administered, the therapeutically effective amount may be a
jointly effective amount. The compounds described herein inhibit the protease
activity of human cathepsin S, an enzyme involved in the immune response. In
preferred embodiments, cathepsin S inhibition is selective. As such, the
disclosed compounds and compositions are useful in the prevention, inhibition,
or treatment of autoimmune diseases such as lupus, rheumatoid arthritis, and
asthma, and for the prevention, inhibition, or treatment of tissue transplant
rejection.
Additional features and advantages of the invention will become
apparent from the detailed description below, including examples, and the
appended claims.

Detailed Description of the Invention
The invention features pyrazole compounds of formula (I), methods of
making them, compositions containing them, and methods of using them to
treat diseases and conditions, including those mediated by Cathepsin S.
A. Terms
The following terms are defined below and by their usage throughout
this disclosure.
"Alky!" includes optionally substituted straight chain and branched
hydrocarbons with at least one hydrogen removed to form a radical group.
Alkyl groups include methyl, ethyl, propyl, isopropyl, butyl, isobutyl, t-butyl, 1-
methylpropyl, pentyl, isopentyl, sec-pentyl, hexyl, heptyl, octyl, and so on.
Alkyl includes cycloalkyl, such as cyclopropyl, cyclobutyl, cyclopentyl, and
cyclohexyl.
"Alkenyl" includes optionally substituted straight chain and branched
hydrocarbon radicals as above with at least one carbon-carbon double bond
(sp2). Alkenyls include ethenyl (or vinyl), prop-1-enyl, prop-2-enyl (or allyl),
isopropenyl (or 1-methylvinyl), but-1-enyl, but-2-enyl, butadienyls, pentenyls,
hexa-2,4-dienyl, and so on. Hydrocarbon radicals having a mixture of double
bonds and triple bonds, such as 2-penten-4-ynyl, are grouped as alkynyls
herein. Alkenyl includes cycloalkenyl. Cis and trans or (E) and (Z) forms are
included within the invention.
"Alkynyl" includes optionally substituted straight chain and branched
hydrocarbon radicals as above with at least one carbon-carbon triple bond (sp).
Alkynyls include ethynyl, propynyls, butynyls, and pentynyls. Hydrocarbon
radicals having a mixture of double bonds and triple bonds, such as 2-penten-
4-ynyl, are grouped as alkynyls herein. Alkynyl does not include cycloalkynyl.

"Alkoxy" includes an optionally substituted straight chain or branched
alkyl group with a terminal oxygen linking the alkyl group to the rest of the
molecule. Alkoxy includes methoxy, ethoxy, propoxy, isopropoxy, butoxy, i-
butoxy, pentoxy and so on. "Aminoalkyl", "thioalkyl", and "surfonytalkyl" are
analogous to alkoxy, replacing the terminal oxygen atom of alkoxy with,
respectively, NH (or NR), S, and SO2. Heteroalkyl includes alkoxy, aminoalkyl,
thioalkyl, and so on.
"Aryl" includes phenyl, naphthyl, biphenyiyl, tetrahydronaphthyl, and so
on, any of which may be optionally substituted. Aryl also includes arylalkyl
groups such as benzyl, phenethyl, and phenylpropyl. Aryl includes a ring
system containing an optionally substituted 6-membered carbocyclic aromatic
ring, said system may be bicyclic, bridge, and/or fused. The system may
include rings that are aromatic, or partially or completely saturated. Examples
of ring systems include indenyl, pentalenyl, 1-4-dihydronaphthyl, indanyl,
benzimidazolyl, benzothiophenyl, indolyl, benzofuranyl, isoquinolinyl, and so
on.
"Heterocyclyl" includes optionally substituted aromatic and nonaromatic
rings having carbon atoms and at least one heteroatom (O, S, N) or
heteroatom moiety (SO2, CO, CONH, COO) in the ring. Unless otherwise
indicated, a heterocyclic radical may have a valence connecting it to the rest of
the molecule through a carbon atom, such as 3-furyl or 2-imidazolyl, or through
a heteroatom, such as N-piperidyl or 1-pyrazolyl. Preferably a monocyclic
heterocyclyl has between 4 and 7 ring atoms, or between 5 and 6 ring atoms;
there may be between 1 and 5 heteroatoms or heteroatom moieties in the ring,
and preferably between 1 and 3. A heterocyclyl may be saturated,
unsaturated, aromatic (e.g., heteroaryl), nonaromatic, or fused.
Heterocyclyl also includes fused, e.g., bicyclic, rings, such as those
optionally condensed with an optionally substituted carbocyclic or heterocyclic
five- or six-membered aromatic ring. For example, "heteroaryl" includes an

optionally substituted six-membered heteroaromatic ring containing 1,2 or 3
nitrogen atoms condensed with an optionally substituted five- or six-
memebered carbocyclic or heterocyclic aromatic ring. Said heterocyclic five- or
six-membered aromatic ring condensed with the said five- or six-membered
aromatic ring may contain 1,2 or 3 nitrogen atoms where it is a six-membered
ring, or 1, 2 or 3 heteroatoms selected from oxygen, nitrogen and sulfur where
it is a five-membered ring.
Examples of hetenocyclyls include thiazoylyl, furyl, pyranyl,
isobenzofuranyl, pyrrolyl, imidazolyl, pyrazolyl, isothiazolyl, isoxazolyl, pyridyl,
pyrazinyl, pyrimidinyl, pyridazinyl, indolizinyl, isoindoiyl, indolyl, indazolyl,
purinyl, quinolyl, furazanyl, pyrrolidinyl, pyrrolinyl, imdazolidinyl, imidazolinyl,
pyrazolidinyl, pyrazolinyl, piperidyl, piperazinyl, indolinyl, and morpholinyl. For
example, preferred heterocyclyls or heterocyclic radicals include morpholinyl,
piperazinyl, pyrrolidinyl, pyridyl, cyclohexylimino, cycloheptylimino,and more
preferably, piperidyl.
Examples illustrating heteroaryl are thienyl, furanyl, pyrrolyl, imidazolyl,
oxazolyl, thiazolyl, benzothienyl, benzofuranyl, benzimidazoiyl, benzoxazolyl,
benzothiazolyl.
"Acyl" refers to a carbonyl moiety attached to either a hydrogen atom
(i.e., a formyl group) or to an optionally substituted alkyl or alkenyl chain, or
heterocyclyl.
"Halo" or "halogen" includes fluoro, chloro, bromo, and iodo, and
preferably chloro or bromo as a substituent.
"Alkanediyl" or "alkylene" represents straight or branched chain
optionally substituted bivalent alkane radicals such as, for example, methylene,
ethylene, propylene, butylene, pentylene or hexylene.

"Alkenediyl" represents, analogous to the above, straight or branched
chain optionally substituted bivalent alkene radicals such as, for example,
propenylene, butenylene, pentenylene or hexenylene. In such radicals, the
carbon atom linking a nitrogen preferably should not be unsaturated.
"Aroyl" refers to a carbonyl moiety attached to an optionally substituted
aryl or heteroaryl group, wherein aryl and heteroaryl have the definitions
provided above. In particular, benzoyl is phenylcarbonyl.
As defined herein, two radicals, together with the atom(s) to which they
are attached may form an optionally substituted 4- to 7-, 5 - to 7-, or a 5- to 6-
membered ring carbocyclic or heterocyclic ring, which ring may be saturated,
unsaturated or aromatic. Said rings may be as defined above in the Summary
of the invention section. Particular examples of such rings are as follows in the
next section.
"Pharmaceutically acceptable salts, esters, and amides" include
carboxylate salts (e.g., C 1-8alkyl, cycloalkyl, aryl, heteroaryl, or non-aromatic
heterocyclic) amino acid addition salts, esters, and amides which are within a
reasonable benefit/risk ratio, pharmacologically effective and suitable for
contact with the tissues of patients without undue toxicity, irritation, or allergic
response. Representative salts include hydrobromide, hydrochloride, sulfate,
bisulfate, nitrate, acetate, oxalate, valerate, oleate, palmitate, stearate, laurate,
borate, benzoate, lactate, phosphate, tosylate, citrate, maleate, fumarate,
succinate, tartrate, naphthylate, mesylate, glucoheptonate, lactiobionate, and
laurylsulfonate. These may include alkali metal and alkali earth cations such
as sodium, potassium, calcium, and magnesium, as well as non-toxic
ammonium, quaternary ammonium, and amine cations such as tetramethyl
ammonium, methylamine, trimethylamine, and ethylamine. See example, S.M.
Berge, et al., "Pharmaceutical Salts," J. Pharm. Sci., 1977, 66:1-19 which is
incorporated herein by reference. Representative pharmaceutically acceptable
amides of the invention include those derived from ammonia, primary C 1-6 alkyl
amines and secondary di (C 1-6alkyl) amines. Secondary amines include 5- or
6-membered heterocyclic or heteroaromatic ring moieties containing at least

one nitrogen atom and optionally between 1 and 2 additional heteroatoms.
Preferred amides are derived from ammonia, C 1-3alkyl primary amines, and di
(C 1-2alkyl)amines. Representative pharmaceutically acceptable esters of the
invention include C 1-7alkyl, C 5-7cycloalkyl, phenyl, and phenyl(C 1-6)alkyl
esters. Preferred esters include methyl esters.
"Patient" or "subject" includes mammals such as humans and animals
(dogs, cats, horses, rats, rabbits, mice, non-human primates) in need of
observation, experiment, treatment or prevention in connection with the
relevant disease or condition. Preferably, the patient or subject is a human.
"Composition" indudes a product comprising the specified ingredients
in the specified amounts as well as any product which results directly or
indirectly from combinations of the specified ingredients in the specified
amounts.
Therapeutically effective amount" or "effective amount" means that
amount of active compound or pharmaceutical agent that elicits the biological or
medicinal response in a tissue system, animal or human that is being sought by
a researcher, veterinarian, medical doctor or other clinician, which includes
alleviation of the symptoms of the disease or disorder being treated.
Concerning the various radicals in this disclosure and in the claims,
three general remarks are made. The first remark concerns valency. As with
all hydrocarbon radicals, whether saturated, unsaturated or aromatic, and
whether or not cyclic, straight chain, or branched, and also similarly with all
heterocyclic radicals, each radical includes substituted radicals of that type and
monovalent, bivalent, and multivalent radicals as indicated by the context of
the claims. The context will indicate that the substituent is an alkylene or
hydrocarbon radical with at least two hydrogen atoms removed (bivalent) or
more hydrogen atoms removed (multivalent). An example of a bivalent radical
linking two parts of the molecule is G in formula (I) which links two rings.

Second, radicals or structure fragments as defined herein are
understood to include substituted radicals or structure fragments. Hydrocarbyls
include monovalent radicals containing carbon and hydrogen such as alkyl,
alkenyl, alkynyl, cycloalkyl, and cycloalkenyl (whether aromatic or unsaturated),
as well as corresponding divalent radicals such as alkylene, alkenylene,
phenylene, and so on. Heterocarbyls include monovalent and divalent radicals
containing carbon, hydrogen, and at least one heteroatom. Examples of
monovalent heterocarbyls include acyl, acyloxy, alkoxyacyl, heterocyclyl,
heteroaryl, aroyl, benzoyl, dialkylamino, hydroxyalkyl, and so on. Using "alky!"
as an example, "alkyl" should be understood to include substituted alkyl having
one or more substitutions, such as between 1 and 5, 1 and 3, or 2 and 4
substituents. The substituents may be the same (dihydroxy, dimethyl), similar
(chlorofluoro), or different (chtorobenzyl- or aminomethyl-substituted).
Examples of substituted alkyl include haloalkyl (such as fluoromethyl,
chloromethyl, difluoromethyl, perchloromethyl, 2-bromoethyl, perfluoromethyl,
and 3-iodocyclopentyl), hydroxyalkyl (such as hydroxymethyl, hydroxyethyl, 2-
hydroxypropyl, aminoalkyl (such as aminomethyl, 2-aminoethyl, 3-aminopropyl,
and 2-aminopropyl), nitroalkyl, alkylalkyl, and so on. A di(C 1-6 alkyl)amino
group includes independently selected alkyl groups, to form, for example,
methylpropylamino and isopropylmethylamino, in addition dialkylamino groups
having two of the same alkyl group such as dimethyl amino or diethylamino.
Third, only stable compounds are intended. For example, where there
is an NR'R" group, and R can be an alkenyl group, the double bond is at least
one carbon removed from the nitrogen to avoid enamine formation. Similarly,
where a dashed line is an optional sp2 bond, if it is absent, the appropriate
hydrogen atom(s) is(are) included.

Preferred substitutions for Ar include methyl, methoxy, fluoromethyl,
difluoromethyl, perfluoromethyl (trffluorornethyl), 14kJOfoethyl, 2-fluoroethyl,
ethoxy, fluoro, chloro, and bromo, and particularly methyl, bromo, chloro,
perfluoromethyl, perfluoromethoxy, methoxy, and fluoro. Preferred substitution
patterns for Ar are 4-substituted or 3,4-disubstituted phenyl. Compounds of the
invention are further described in the next section.

B. Compounds
The invention features compounds of formula (I) as described in the
Summary section.
Preferred compounds include those wherein:
(a) one of S, T, Y, and Z is nitrogen;
(b) S and T are CR3 and CR2, respectively;
(c) S, T, Y, and Z are CR3, CR2, CR20, and CR21, respectively;
(d) (1) Z is N, Y is N, S is CR3, and T is CR2; or (2) S is N, T is N, Y is
CR20, and Z is CR21;
(e) R2 is hydrogen, halogen, C1-5 alkoxy, cyano, ReRfN, or a 5-6
membered heterocyclyl;
(f) R3 is hydrogen, halogen, C1-5 alkoxy, C1-5 alkyl, cyano, R17OC=O, or
RgRhN, where Rg and Rhare H or C 1-5 alkyl, or are taken together to
form a 5-6 membered heterocyclyl;
(g) each of R2 and R3 is independently selected from hydrogen, halogen,
and a 5-6 membered heterocyclyl;
(h) R5 and R6 are independently selected from hydrogen and C1-3 alkyl;
(i) one of R5 and R6 is H;
(j) R5 and R6 are each H;
(k) one of R7 and R8 is H and the other is 5-7 membered carbocyclyl or
heterocyclyl;
(I) R7 and R8 are taken together to form an optionally substituted 5- to
7- membered carbocyclic or heterocyclic ring;
(m) R7 and R8 are taken together to form a six-membered heterocyclyl;
(n) R7 and R8 taken together form a 5-7 membered heterocyclyl
optionally N-substituted with Rt(C=O)-, RtSO2, or NHRU(C=O)-
wherein Rt is C 1-6 alkyl, phenyl, or C 2-5 heterocyclyl and Ru is H, C 1-6
alkyl, phenyl, or C 2-5 heterocyclyl;

(o) each of Rc, Re, Rm, and R° is independently selected from hydrogen.
C1-5 alkyl, C2-8acyl, (C 1-5 alkyl)OC=O, and the respective RRNC=O,
RSO, RSO2, and RRNSO2 groups;
(p) each of Rc, Rd, R°, Rh, R°, Rf, and Rp is independently selected from
hydrogen and C1-5alkyl; or, independently, Re and Rf, Rg and Rh, or
R° and Rp taken together form an optionally substituted 4- to 7-
membered carbocyclic or heterocyclic ring;
(q) Re and Rf taken together are morpholinyl, piperidinyl, or pyrrolidinyl;
(r) each of R43, R44, R45, R46, R47, R48, Ri, Rj, Rk and Rl independently is
hydrogen or C1-5alkyl;
(s) each of R9, R11, R14, R15, R16and R17 is independently C1-5alkyl;
(t) R° is C1-5alkyl, C 2-5 acyl, R9OC=O, R18R19NC=O, R9SO, R9SO2, or
R18R19NSO2; and Rh is H or C1-5 alkyl; alternatively, R° and Rh can be
taken together to form an optionally substituted 5- to 6-membered
heterocyelyl;
(u) R° and Rh are each C 1-3 alkyl;
(v) R18 and R19 independently are hydrogen or C1-5alkyl;
(w) n is 0 or 1; or n is 1;
(x) G is C3-4 alkanedryl, optionally substituted with hydroxy, halogen, [(L)-
C 1-5 alkylene]amino, or (L)-C1-5alkyloxy;
(y) G is C3 alkanediyl, optionally substituted with hydroxy;
(z) R20 and R21 are independently selected from hydrogen, halogen, C1-5
alkoxy, C1-5 alkyl, cyano, nitro, 4-7 membered heterocyelyl, and
R°RpN or RcRdN, respectively;
(aa) R20 and R21 are independently selected from hydrogen, halogen,
5- to 6-membered heterocyelyl, and R°RPN or RcRdN, respectively;
(bb) Ar represents a monocyclic ring, optionally substituted with 1 to 2
substituents selected from halogen, C1-5alkyl, cyano, nitro, R22R23N,
C1-3haloalkyl, and C1-3haloalkoxy;
(cc) Ar is a six-membered aromatic ring monosubstituted at the 4-
position with halogen, methyl, CF3, or OCF3, or disubstituted at the 3-
and 4-positions with substituents independently selected from
halogen, CF3, methyl, and OCF3;

(dd) each of R22, R23, and R24 is independently hydrogen or C1-5 alkyl;
(ee) R25 and R26 independently are hydrogen or C1-5alkyl,
or, alternatively, R25 and R26 are taken together to form an optionally
substituted 4- to 7- membered heterocyclic ring, which ring may be
saturated, unsaturated or aromatic;
(ff) R25 and R26 independently are hydrogen or C1-5 alkyl;
(gg) Q is NR33 or S;
(hh) Q is NR33, R33 is H or C2-5 heterocyclyl, and R32 is H, C 1-5 alkyl, C1-5
hydroxyalkyl, -(C=O)NRVRX, CHO, or C 1-6 alkoxycarbonyl, wherein
each of Rv and Rx is independently selected from H, C 1-5
hydroxyalkyl, (C 1-6 heterocyclyl)-C 1-5 alkylene, and C 1-5
aminoalkylene;
(ii) wherein Q is S and R33 is NR36R37(C=O)- where each of R36 and R37
are independently selected from hydrogen and C1-5 alkyl;
(jj) R35 is selected from hydrogen and C1-5 alkyl; R36 and R37 are each
independently selected from hydrogen, C1-5 alkyl, or, alternatively,
R36 and R37 can be taken together to form an optionally substituted 4-
to 7-membered heterocyclic ring;
(kk) Y is nitrogen or R20C; Z is nitrogen or R21C; T is nitrogen or R2C;
S is nitrogen or R3C; provided between 0 and 2 of S, T, Y, and Z are
nitrogen; for example 1 of them is N;
(II) R2 is hydrogen, halogen, hydroxy, C1-5 alkoxy, C1-5 alkyl, 5- to 6-
membered heterocyclyl, or ReRfN;
(mm) R3 is hydrogen, halogen, C1-5 alkoxy, hydroxy, C1-5 alkyl, 5- to
6-membered heterocyclyl, or R°RhN;
(nn) R7 and R8 independently are taken together to form an optionally
substituted 5- to 7- membered unsaturated heterocyclic ring;
(oo) each of Ra- Re, Rm , and R° is independently selected from
hydrogen, C1-5 alkyl, C 2-8 acyl, (C1-5 alkyl)OC=O, and the respective
RRNC=O, RSO, RSO2, and RRNSO2 groups;
(pp) each of Rb, Rf, Rn, and Rp, is independently selected from
hydrogen and C1-5alkyl; each of R9, R11, R14, R15, R16, R17, R40, R41
and R42 is independently C1-5 alkyl; and each of Rc, Rd, Ri, Rj, R43,

R44, R45, R46, R47, Rk and R1 are independently are hydrogen or C1-5
alkyl;
(qq) R9 is hydrogen, or C1-5 alkyl, C 2-8 acyl, R9OC=O, R18R19NC=O,
R9SO, R9SO2, or R18R19NSO2; Rh is hydrogen or C1-5 alkyl;
alternatively, R° and Rh can be taken together to form an optionally
substituted 4- to 7- membered carbocyclic or heterocydic ring, which
ring may be saturated, unsaturated or aromatic; R18 and R19
independently are hydrogen or C1-5 alkyl; n is 0 or 1;
(rr) G is C3-4 alkenedtyl or C3-4 alkanediyl, optionally substituted with
hydroxy, halogen, C1-5alkyloxy, oxo, hydroximino, CO2Rk, RKRlNCO2,
or (L)-C1-5alkoxy; L is amino, mono- or di-C1-5alkylamino, pyrrolidinyl,
morpholinyl, piperidinyl homopiperidinyl, or piperazinyl, available ring
nitrogens being optionally with C1-5 alkyl, benzyl, C2-5acyl, or C1-5
alkyloxycarbonyl;
(ss) R20 and R21 are independently selected from hydrogen, halogen,
C1-5alkoxy, C1-5 alkyl, cyano, nitro, and R°RPN; alternatively, R3 and
R20 or R3 and R21 can be taken together to form an optionally
substituted 5- or 6-membered carbocyclic or heterocydic ring, which
ring may be saturated, unsaturated or aromatic; and Ar represents a
monocyclic or bicyclic aryl or heteroaryl ring, optionally substituted
with hydrogen, halogen, C1-5alkoxy, C1-5alkyl, cyano, nitro, R22R23N,
R24SO2, R24OC=O, R25R26NC=O, CF3, OCF3, SCF3, or C1-5 alkylthio;
R22 is hydrogen, C1-5alkyl, phenyl, benzyl, phenethyl, C2-5heteroaryl,
C2-8acyl, aroyl, R24OC=O, R25R26NC=O, R24SO, R24SO2, or
R25R26NSO2; R23 is hydrogen or C1-5alkyl; alternatively, R22 and R23
can be taken together to form an optionally substituted 4- to 7-
membered carbocyclic or heterocydic ring, which ring may be
saturated, unsaturated or aromatic; R24 is hydrogen or C1-5alkyl; R25
and R26 are independently hydrogen or C1-5 alkyl; or, alternatively, R25
and R26 can be taken together to form an optionally substituted 4- to
7- membered carbocyclic or heterocydic ring, which ring may be
saturated, unsaturated or aromatic;

(tt) R32 is hydrogen, C1-5alkyl, C1-5 hydroxyalkyl, CHO, C 2-6 acyl, C 1-6
alkoxycarbonyl, or -(C=O)NRVRX, wherein each of RVRX is
independently selected from H, C 1-5 alkyl, C1-5 hydroxyalkyl, C 3-8
acyloxy, (amlno)C 1-6 alkylene, (C1-5 heterocyclyl)C1-5 alkylene, or C
1-6 alkoxycarbonyl; and Q is NR33 or S; R33 represents hydrogen, C1-5
alkyl, phenyl, benzyl, (C 2-5 heterocyclyl)C1-5 alkylene, C 2-8 acyl,
aroyl, R35OC=O, R38R37NC=O, R35SO2 and R36R37NSO2; R35 is
selected from hydrogen and C1-5 alkyl; R36 and R37 are each
independently selected from hydrogen and C1-5 alkyl;
(uu) one of R5 and R6 is H, R7 and R8 are taken together to form an
optionally substituted 6- membered carbocyclic or heterocydic ring;
a~d Ar represents a monocyclic ring, optionally substituted with 1 to
2 abstituents selected from halogen, C1-5 alkyl, cyano, nitro, R22R23N,
CF3 and OCF3;
(w) both R5 and R6 are each H, and
(ww) Ar is a six membered ring substituted with halogen, CF3, methyl,
halomethyl, or OCF3, at the 3- or 4- position, or disubstituted at the
3- and 4- positions;
(xx) R7 and R8 taken together form pyridinyl, pyrimidinyl, or
piperazinyl, optionaly N-substituted with -(C=O)Rt, SO2-Rt, or -
(C=O)NHRU;
(yy) Re and Rf taken together are independently morpholinyl,
piperidyl, or pyrrolidinyl, optionally substituted;
(zz) the dashed line adjacent C-R6 is absent;
(aaa) or combinations of the above.
Specific preferred compounds include those in the Examples below,
such as:
1-[1-{2-Hydroxy-3-[4-(1H-indol-3-yl)-piperidin-1-yl]-propyl}-3-(4-trifluoromethyl-
phenyl)-1,4,6,7-tetrahydro-pyrazolo[4,3-c]pyridin-5-yl]-ethanone; 1-[4-(5-
Fluoro-1H-indol-3-yl)-piperidin-t-yl]-3-{5-methanesulfonyl-3-(4-trifluoromethyl-
phenyl)-4,5,6,7-tetrahydro-pyrazoto[4,3-c]pyridin-1-yl]-propan-2-ol; 1 -[3-(4-
Bromo-phenyl)-5-memanesulfonyl-4,5,6,7-tetrahydro-pyrazolo[4,3-c]pyridin-1-

yl]-3-[4-(5-chloro-1H-indol-3-yl)-piperidin-1-yl]-propan-2-ol; 1-[3-(4-Bromo-
phenyl)-5-methanesulfonyl-4,5,6,7-tetrahydro-pyrazolo[4,3-c]pyridin-1-yl]-3-[4-
(6-chloro-2-methyl-1H-indol-3-yl)-piperidin-1-yl]-propan-2-ol; 1-[5-
Methanesulfonyl-3-(4-trifluoromethyl-phenyl)-4,5,6,7-tetrahydro-pyrazolo[4,3-
c]pyridin-1-yl]-3-[4-(5-methyl-1H-indol-3-yl)-piperidin-1-yl]-propan-2-ol; 3-(1-{2-
Hydroxy-3-[5-methanesulfonyl-3-(4-trifluoromethyl-phenyl)-4,5,6,7-tetrahydro-
pyrazolo[4,3-c]pyridin-1-yl]-propyl}-piperidin-4-yl)-1H-indole-5-carbonitrite; 1-[5-
Methanesulfonyl-3-(4-trifluorornethyl-phenyl)-4,5,6,7-tetrahydro-pyrazolo[4,3-
c]pyridin-1-yl]-3-[4-(5-methoxy-1H-indol-3-yl}-piperidin-1-yl]-propan-2-ol; 3-(1-
{2-Hydroxy-3-[5-methanesulfonyl-3-(4-trifluoromethyl-phenyl)-4,5,6,7-
tetrahydro-pyrazolo[4,3-c]pyridin-1-yl]-propyl}-piperidin-4-yl)-1H-indole-5-
carboxylic acid ethyl ester; 1-[4-4-(6-Chloro-1H-indol-3-yl)-piperidin-1-yl]-3-[6-
methanesulfonyl-3-(4-trifluoromethyl-phenyl)-4,5,6,7-tetrahydro-pyrazolo[4,3-
c]pyridin-1-yl]-propan-2-ol; 1-{1-(3-{4-[6-Chloro-1-(2-morpholin-4-yl-ethyl)-1H-
indol-3-yl]-piperidin-1-yl}-2-hydroxy-propyl)-3-(4-trifluoromethyl-phenyl)-1,4,6,7-
tetrahydro-pyrazolo[4,3-c]pyridin-5-yl]-ethanone; 1-[5-Methanesulfonyl-3-(4-
trlfluoromethyl-phenyl)-4,5,6,7-tetrahydro-pyrazolo[4,3-c]pyridin-1-yl]-3-[4-(1H-
pyrrolo[3,2-b]pyridin-3-yl)-piperidin-1-yl]-propan-2-ol; 1-[5-Methanesulfonyl-3-
(4-trifluoromethyl-phenyl)-4,5,6,7-tetrahydro-pyrazolo[4,3-c]pyridin-1-yl]-3-[4-
(1H-pyrrolo[2,3-c]pyridin-3-yl)-piperidin-1-yl]-propan-2-ol; 1-[5-
Methanesulfonyl-3-(4-trifluoromethyl-phenyl)-4,5,6,7-tetrahydro-pyrazolo[4,3-
c]pyridin-1-yl]-3-[4-(5-oxy-1H-pyrrolo[3,2-c]pyridin-3-yl)-piperidin-1-yl]-propan-2-
ol; 1-[4-(5-Dimethylamino-1H-pyrrolo[3,2-b]pyridin-3-yl)-piperidin-1-yl]-3-[5-
methanesulfonyl-3-(4-trifluoromethyl-phenyl)-4,5,6,7-tetrahydro-pyrazolo[4,3-
c]pyridin-1-yl]-propan-2-ol; 1-[4-(5-Dimethylamino-1H-pyrrolo[2,3-c]pyridin-3-
yl)-piperidin-1-yl]-3-[5-methanesulfonyl-3-(4-trifluoromethyl-phenyl)-4,5,6,7-
tetrahydro-pyrazolo[4,3-c]pyridin-1-yl]-propan-2-ol; 3-(1-{2-Hydroxy-3-[5-
methanesulfonyl-3-(4-trifluoromethyl-phenyl)-4,5,6,7-tetrahydro-pyrazolo[4,3-
c]pyridin-1-yl]-propyl}-piperidin-4-yl)-1H-pyrrolo[2,3-b]pyridine-6-carbonitrile ; 1-
[5-Methanesulfonyl-3-(4-trifluoromethyl-phenyl)-4,5,6,7-tetrahydro-pyrazolo[4,3-
c]pyridin-1-yl]-3-{4-[1-(2-morpholin-4-yl-ethyl)-1H-pyrrolo[2,3-b]pyridin-3-yl]-
piperidin-1-yl}-propan-2-ol; 1-[5-Methanesulfonyl-3-(4-trifluoromethyl-phenyl)-
4,5,6,7-tetrahydro-pyrazolo[4,3-c]pyridin-1-yl]-3-[4-(7-morpholin-4-yl-1H-

pyrrolo[2,3-c]pyridin-3-yl)-piperidin-1-yl]-propan-2-ol; 1-[4-(6-Fluoro-2-
hydroxymethyl-benzo[b]thiophen-3-yl)-piperidin-1-yl]-3-[5-methanesulfonyl-3-
(4-trlfluoromethyl-phenyl)-4,5,6,7-tetrahydro-pyrazolo[4,3-c]pyridin-1-yl]-
propan-2-ol; 6-Fluono-3-(1-{2-hydroxy-3-[5-methanesulfonyl-3-(4-
trifluoromethyl-phenyl)-4,5,6,7-tetrahydro-pyrazolo[4,3-c]pyridin-1-yl]-propyl}-
piperidin-4-yl)-benzo[b]thiophene-2-carbaldehyde; 6-Fluoro-3-(1-{2-hydroxy-3-
[5-methanesulfonyl-3-(4-trifluoromethyl-phenyl)-4,5,6,7-tetrahydro-pyrazolo[4,3-
c]pyridin-1-yl]-propyI}-pjperidin-4-yl)-benzo[b]thiophene-2-carboxylic acid
methyl ester; 6-Fluoro-3-(1-{3-[5-methanesulfonyl-3-(4-trifluoromethyl-phenyI)-
4,5,6,7-tetrahydro-pyrazolo[4,3-c]pyridin-1-yl]-propyl}-piperidin-4-
yl)benzo[b]thiophene-2-carboxylic acid amide ; and 6-Fluoro-3-(1-{3-[5-
methanesulfonyl-3-(4-trifluoromethyl-phenyl)-4,5,6,7-tetrahydro-pyrazolo[4,3-
c]pyridin-1-yl]-propyl}-piperidin-4-yl)benzo[b]thiophene-2-carboxylic.
Furthermore, preferred compounds include those wherein Ar is selected
from 4-trifluoromethylphenyl, 4-bromophenyl, 4-chlorophenyl, 4-chloro-3-
methylphenyl and 3,4-dichlorophenyl.
More preferred compounds include those in Examples 4, 9,13, and 26.

Related Compounds
The invention provides the disclosed compounds and closely related,
pharmaceutically acceptable forms of the disclosed compounds, such as salts,
esters, amides, acids, hydrates or solvated forms thereof; masked or protected
forms; and racemic mixtures, or enantiomerically or optically pure forms.
Related compounds also include compounds of the invention that have been
modified to be detectable, e.g., isotopically labelled with 18F for use as a probe
in positron emission tomography (PET) or single-photon emission computed
tomography (SPECT).
The invention also includes disclosed compounds having one or more
functional groups (e.g., hydroxyl, amino, or carboxyl) masked by a protecting
group. See, e.g., Greene and Wuts, Protective Groups in Organic Synthesis,
3rd ed., (1999) John Wiley & Sons, NY. Some of these masked or protected
compounds are pharmaceutically acceptable; others will be useful as
intermediates. Synthetic intermediates and processes disclosed herein, and
minor modifications thereof, are also within the scope of the invention.

HYDROXYL PROTECTING GROUPS
Protection for the hydroxyl group includes methyl ethers, substituted
methyl ethers, substituted ethyl ethers, substitute benzyl ethers, and silyl
ethers.
Substituted Methyl Ethers
Examples of substituted methyl ethers include methyoxymethyl,
methylthiomethyl, t-butylthiomethyl, (phenyldimethylsilyl)methoxymethyl,
benzyloxymethyl, p-methoxybenzyloxymethyl, (4-methoxyphenoxy)methyl,
guaiacolmethyl, t-butoxymethyl, 4-pentenyloxymethyl, siloxymethyl, 2-
methoxyethoxymethyl, 2,2,2-trichloroethoxymethyl, bis(2-chloroethpxy)methyl,
2-(trimethylsilyl)ethoxymethyl,tetrahydropyranyl, 3-bromotetrahydropyranyl,
tetrahydrothiopyranyl, 1-methoxycyclohexyl, 4-methoxytetrahydropyranyl, 4-
methoxytetrahydrothiopyranyl, 4-methoxytetrahydrothiopyranyl S,S-dioxido, 1-
[(2-chloro-4-methyl)phenyl]-4-methoxypiperidin-4-yl, 1,4-dioxan-2-yl,
tetrahydrofuranyl, tetrahydrothiofuranyl and 2,3,3a,4,5,6,7,7a-octahydro-7,8,8-
trimethyl-4,7-methanobenzofuran-2-yl.
Substituted Ethyl Ethers
Examples of substituted ethyl ethers include 1-ethoxyethyl, 1-(2-
chloroethoxy)ethyl, 1-methyl-1-methoxyethyl, 1-methyl-1-benzyloxyethyl, 1-
methyl-1-benzyloxy-2-fluoroethyl, 2,2,2-trichloroethyl, 2-trimethylsilylethyl, 2-
(phenylselenyl)ethyl, t-butyl, allyl, p-chlorophenyl, p-methoxyphenyl, 2,4-
dinitrophenyl, and benzyl.
Substituted Benzyl Ethers
Examples of substituted benzyl ethers include p-methoxybenzyl, 3,4-
dimethoxybenzy/, o-nitrobenzyl, p-nitrobenzyl, p-halobenzy), 2,6-
dichlorobenzyl, p-cyanobenzyl, p-phenylbenzyl, 2- and 4-picolyl, 3-methyl-2-
picolyl N-oxido, diphenylmethyl, p, p'-dinitrobenzhydryl, 5-dibenzosuberyl,

triphenylmethyl, ?-naphthyldiphenylmethyl, p-methoxyphenyldiphenylmethyl,
di(p-methoxyphenyl)phenylrnethyl, tri(p-methoxyphenyl)methyl, 4-(4'-
bromophenacyloxy)phenyldiphenylmethyl, 4,4',4"-tris(4,5-
dichlorophthalimidophenyl)methyl, 4,4',4"-tris(levulinoyloxyphenyl)methyl,
4,4',4"-tris(benzoyloxyphenyl)methyl, 3-(/midazol-1-ylmethyl)bis(4',4"-
dimethoxyphenyl)methyl, 1,1-bis(4-methoxyphenyl)-1'-pyrenylmethyl, 9-anthryl,
9-(9-phenyl)xanthenyl, 9-(9-phenyl-10-oxo)anthryl, 1,3-benzodithiolan-2-yl, and
benzisothiazolyl S,S-dioxido.
Silyl Ethers
Examples of silyl ethers include trimethylsilyl, triethylsilyl, triisopropylsilyl,
dimethylisopropylsilyl, diethylisopropylsilyl, dimethylthexyisilyl, t-
butyldimethylsilyl, t-butyldiphenylsilyl, tribenzylsilyl, tri-p-xylylsilyl, triphenylsilyl,
diphenylmethylsilyl, and t-butyimethoxyphenylsilyl.
Esters
In addition to ethers, a hydroxyl group may be protected as an ester.
Examples of esters include formate, benzoylformate, acetate, chloroacetate,
dichloroacetate, trichloroacetate, trifluoroacetate, methoxyacetate,
triphenylmethoxyacetate, phenoxyacetate, p-chlorophenoxyacetate, p-P-
phenylacetate, 3-phenylpropionate, 4-oxopentanoate(levulinate), 4,4-
(ethylenedithio)pentanoate, pivaloate, adamantoate, crotonate, 4-
methoxycrotonate, benzoate, p-phenylbenzoate, 2,4,6-
trimethylbenzoate(mesitoate)
Carbonates
Examples of carbonate protecting groups include methyl, 9-
fluorenylmethyl, ethyl, 2,2,2-trichloroethyl, 2-(trimethyisilyl)ethyl, 2-
(phenylsulfonyl)ethyl, 2-(triphenylphosphonio)ethyl, isobutyl, vinyl, allyl, p-
nitrophenyl, benzyl, p-methoxybenzyl, 3,4-dimethoxybenzyl, o-nitrobenzyl, p-
nitrobenzyl, S-benzyl thiocarbonate, 4-ethoxy-1-naphthyl, and methyl
dithiocarbonate.

Assisted Cleavage
Examples of assisted cleavage include 2-iodobenzoate, 4-azidobutyrate,
4-nitro-4-methylpentanoate, o-(dibromomethyl)benzoate, 2-
formylbenzenesulfonate, 2-(methylthiomethoxy)ethyl carbonate, 4-
(methylthiomethoxy)butyrate, and 2-(methylthiomethoxymethyl)benzoate.
Miscellaneous Esters
Examples of miscellaneous esters include 2,6-dichloro-4-
methylphenoxyacetate, 2,6-dichloro-4-(1,1,3,3-
tetramethylbutyl)phenoxyacetate, 2,4-bis(1,1-dimethylpropyl)phenoxyacetate,
chlorodiphenylacetate, isobutyrate, monosuccinoate, (E)-2-methyl-2-
butenoate(tigloate), o(methoxycarbonyl)benzoate, p-P-benzoate, ?-
naphthoate, nitrate, alkyl N,N,N',N'-tetramethylphosphorodiamidate, N-
phenylcarbamate, borate, dimethylphosphinothioyl, and 2,4-
dinitrophenylsulfenate.
Sulfonates
Examples of sulfonates include sulfate, methanesulfonate(mesylate),
benzylsulfonate, and tosylate.
AMINO PROTECTING GROUPS
Protection for the amino group includes carbamates, amides, and
special -NH protective groups.
Examples of carbamates include methyl and ethyl carbamates,
substituted ethyl carbamates, assisted cleavage carbamates, photolytic
cleavage carbamates, urea-type derivatives, and miscellaneous carbamates.

Carbamates
Examples of methyl and ethyl carbamates include methyl and ethyl, 9-
fluorenylmethyl, 9-(2-sulfo)fluorenylmethyl, 9-(2,7-dibromo)fluorenylmethyl, 2,7-
di-t-butyl-[9-(10,10-dioxo-10,10,10',10-tetrahydrothioxanthyl)]methyl, and 4-
methoxyphenacyl.
Substituted Ethyl
Examples of substituted ethyl carbamates include 2,2,2-trichloroethyl, 2-
trimethylsilylethyl, 2-phenylethyl, 1-(1-adamantyl)-1-methylethyl, 1,1-dimethyl-
2-haloethyl, 1,1-dimethyl-2,2-dibromoethyl, 1,1-dimethyl-2,2,2-trichloroethyl, 1-
methyl-1-(4-biphenylyl)ethyl, 1-(3,5-di-t-butylphenyl)-1-methylethyl, 2-(2'- and
4'-pyridyl)ethyl, 2-(N,N-dicyclohexylcarboxamido)ethyl, t-butyl, 1-adamantyl,
vinyl, allyl, 1-isopropylallyl, cinnamyl, 4-nitrocinnamyl, 8-quinolyl, N-
hydroxypiperidinyl, alkyldithio, benzyl, p-methoxybenzyl, p-nitrobenzyl, p-
bromobenzyl, p-chlorobenzyl, 2,4-dichlorobenzyl, 4-methylsulfinylbenzyl, 9-
anthrylmethyl and diphenylmethyl.
Assisted Cleavage
Examples of assisted cleavage include 2-methylthioethyl, 2-
methylsulfonylethyl, 2-(p-toluenesulfonyl)ethyl, [2-(1,3-dithianyl)]methyl, 4-
methylthiophenyl, 2,4-dimethylthiophenyl, 2-phosphonioethyl, 2-
triphenylphosphonioisopropyl, 1,1-dimethyl-2-cyanoethyl, m-chloro-p-
acyloxybenzyl, p-(dihydroxyboryl)benzyl, 5-benzisoxazolylmethyl, and 2-
(trifluoromethyl)-6-chromonylmethyl.
Photolytic Cleavage
Examples of photolytic cleavage include m-nitrophenyl, 3,5-
dimethoxybenzyl, o-nitrobenzyl, 3,4-dimethoxy-6-nitrobenzyl, and phenyl(o-
nitrophenyl)methyl.

Urea-Type Derivatives
Examples of urea-type derivatives include phenothiazinyl-(10)-carbonyl
derivative, N' -p-toluenesulfonylaminocarbonyl, and N'-
phenylaminothiocarbonyl.
Miscellaneous Carbamates
Examples of miscellaneous carbamates include t-amyl, S-benzyl
thiocarbamate, p-cyanobenzyl, cyclobutyl, cyclohexyl, cyclopentyl,
cyclopropylmethyl, p-decyloxybenzyl, diisopropylmethyl, 2,2-
dimethoxycarbonylvinyl, o-(N,N-dimethylcarboxamido)benzyl, 1,1-dimethyl-3-
(N,N-dimethylcarboxamido)propyl, 1,1-dimethylpropynyl, di(2-pyridyl)methyl, 2-
furanylmethyl, 2-iodoethyl, isobornyl, isobutyl, isonicotinyl, p-(p'-
methoxyphenylazo)benzyl, 1-methylcyclobutyl, 1-methylcyclohexyl, 1-methyl-1 -
cyclopropylmethyl, 1-methyl-1-(3,5-dimethoxyphenyl)ethyl, 1-methyl-1-(p-
phenylazophenyl)ethyl, 1 -methyl-1-phenylethyl, 1 -methyl-1-(4-pyridyl)ethyl,
phenyl, p-(phenylazo)benzyl, 2,4,6-tri-t-butylphenyl, 4-
(trimethylammonium)benzyl, and 2,4,6-trimethylbenzyl.
Examples of amides include:
Amides
N-formyl, N-acetyl, N-chloroacetyl, N-trichloroacetyl, N-trifluoroacetyl, N-
phenylacetyl, N-3-phenylpropionyl, N-picolinoyl, N-3-pyridylcarboxamide, N-
benzoylphenylalanyl derivative, N-benzoyl, N-p-phenylbenzoyl.
Assisted Cleavage
N-o-nitrophenylacetyl, N-o-nitrophenoxyacetyl, N-acetoacetyl, (N'-
dithiobenzyloxycarbonylamino)acetyl, N-3-(p-hydroxyphenyl)propionyl, N-3-(o-
nitrophenyl)propionyl, N-2-methyl-2-(o-nitrophenoxy)propionyl, N-2-methyl-2-
(o-phenylazophenoxy)propionyl, N-4-chlorobutyryl, N-3-methyl-3-nitrobutyryl,
N-o-nitrocinnamoyl, N-acetylmethionine derivative, N-o-nitrobenzoyl, N-o-
(benzoyloxymethyl)benzoyl, and 4,5-diphenyl-3-oxazoiin-2-one.

Cyclic Imide Derivatives
N-phthalimide, N-dithiasuccinoyl, N-2,3-diphenylmaleoyl, N-2,5-
dimethylpyrrolyl, N-1,1,4,4-tetramethyldisilylazacyclopentane adduct, 5-
substituted 1,3-dimethyl-1,3,5-triazacyclohexan-2-one, 5-substituted 1,3-
dibenzyl-1,3,5-triazacyclohexan-2-one, and 1-substituted 3,5-dinitro-4-
pyridonyl.
SPECIAL - NH PROTECTIVE GROUPS
Examples of special NH protective groups include
N-Alkyl and N-Aryl Amines
N-methyl, N-allyl, N-[2-(trimethylsilyl)ethoxy]methyl, N-3-acetoxypropyl,
N-(1-isopropyl-4-nitro-2-oxo-3-pyrrolin-3-yl), quaternary ammonium salts, N-
benzyl, N-di(4-methoxyphenyl)methyl, N-5-dibenzosuberyl, N-triphenylmethyl,
N-(4-methoxyphenyl)diphenylmethyl, N-9-phenylfluorenyl, N-2,7-dichloro-9-
fluorenylmethylene, N-ferrocenylmethyl, and N-2-picolylamine N'-oxide.
Imine Derivatives
N-1,1-dimethylthiomethylene, N-benzylidene, N-p-methoxybenzylidene,
N-diphenylmethylene, N-[(2-pyridyl)mesityl]methylene, and N-(N',N'-
dimethylaminomethylene).
PROTECTION FOR THE CARBONYL GROUP
Acyclic Acetals and Ketals
Examples of acyclic acetals and ketals include dimethyl, bis(2,2,2-
trichloroethyl), dibenzyl, bis(2-nitrobenzyl) and diacetyl.

Cyclic Acetals and Ketals
Examples of cyclic acetals and ketals include 1,3-dioxanes, 5-
methylene-1,3-dioxane, 5,5-dibromo-1,3-dioxane, 5-(2-pyridyl)-1,3-dioxane,
1,3-dioxolanes, 4-bromomethyl-1,3-dioxolane, 4-(3-butenyl)-1,3-dioxolane, 4-
phenyl-1,3-dioxolane, 4-(2-nitrophenyl)-1,3-dioxolane, 4,5-dimethoxymethyl-
1,3-dioxolane, O,O'-phenylenedioxy and 1,5-dihydro-3H-2,4-benzodioxepin.
Acyclic Dithio Acetals and Ketals
Examples of acyclic dithio acetals and ketals include S,S'-dimethyl,
S,S'-diethyl, S,S'-dipropyl, S,S'-dibutyl, S,S'-dipentyl, S,S'-diphenyl, S,S'-
dibenzyl and S,S'-diacetyl.
Cyclic Dithio Acetals and Ketals
Examples of cyclic dithio acetals and ketals include 1,3-dithiane, 1,3-
dithiolane and 1,5-dihydro-3H-2,4-benzodithiepin.
Acyclic Monothio Acetals and Ketals
Examples of acyclic monothio acetals and ketals include O-trimethylsilyl-
S-alkyl, O-methyl-S-alkyl or -S-phenyl and O-methyl-S-2-(methylthio)ethyl.
Cyclic Monothio Acetals and Ketals
Examples of cyclic monothio acetals and ketals include 1,3-
oxathiolanes.
MISCELLANEOUS DERIVATIVES
O-Substituted Cyanohydrins
Examples of O-substituted cyanohydrins include O acetyl, O-
trimethylsilyl, O-1-ethoxyethyl and O-tetrahydropyrany.

Substituted Hydrazones
Examples of substituted hydrazones include N,N-dimethyl and 2,4-
dinitrophenyl.
Oxime Derivatives
Examples of oxime derivatives include O-methyl, O-benzyl and O-
phenylthiomethyl.
Imines
Substituted Methylene Derivatives, Cyclic Derivatives
Examples of substituted methylene and cyclic derivatives include-
oxazolidines, 1-methyl-2-{1'-hydroxyalkyl)imidazoles, N,N'-
dimethylimidazolidines, 2,3-dihydro-1,3-benzothiazoles, diethylamine adducts,
and methylaluminum bis{2,6-di-t-butyl-4-methylphenoxide)(MAD)complex.

PROTECTION FOR THE CARBOXYL GROUP
Esters
Substituted Methyl Esters
Examples of substituted methyl esters include 9-fluorenylmethyl,
methoxymethyl, methylthiomethyl, tetrahydropyranyl, tetrahydrofuranyl,
methoxyethoxymethyl, 2-(trimethylsilyl)ethoxymethyl, benzyloxymethyl,
phenacyl, p-bromophenacyl, ?-methylphenacyl, p-methoxyphenacyl,
carboxamidomethyl, and N-phthalimidomethyl.
2-Substituted Ethyl Esters
Examples of 2-substituted ethyl esters include 2,2,2-trichloroethyl,
2-haloethyl, ?-chloroalkyl, 2-(trimethylsilyl)ethyl, 2-methylthioethyl, 1,3-
dithianyl-2-methyl, 2-(p-nitrophenylsulfenyl)ethyl, 2-(p-toluenesulfonyl)ethyl,
2-(2'-pyridyl)ethyl, 2-(diphenylphosphino)ethyl, 1 -methyl-1-phenylethyl, t-butyl,
cyclopentyl, cyclohexyl, allyl, 3-buten-1-yl, 4-(trimethylsilyl)-2-buten-1-yl,
cinnamyl, ?-methylcinnamyl, phenyl, p-(methylmercapto)phenyl and benzyl.
Substituted Benzyl Esters
Examples of substituted benzyl esters include triphenylmethyl,
diphenylmethyl, bis(o-nitrophenyl)methyl, 9-anthrylmethyl, 2-(9,10-
dioxo)anthrylmethyl, 5-dibenzosuberyl, 1-pyrenylmethyl, 2-(trifluoromethyl)-6-
chromylmethyl, 2,4,6-trimethylbenzyl, p-bromobenzyl, o-nitrobenzyl, p-
nitrobenzyl, p-methoxybenzyl, 2,6-dimethoxybenzyl, 4-(methylsulfinyl)benzyl, 4-
sulfobenzyl, piperonyl, 4-picolyl and p-P-benzyl.
Silyl Esters
Examples of silyl esters include trimethylsilyl, triethylsilyl,
t-butyldimethylsilyl, i-propyldimethylsilyl, phenyldimethylsilyl and di-t-
butylmethylsilyl.

Activated Esters
Examples of activated esters include thiols.
Miscellaneous Derivatives
Examples of miscellaneous derivatives include oxazoles, 2-alkyl-1,3-
oxazolines, 4-alkyl-5-oxo-1,3-oxazolidines, 5-alkyl-4-oxo-1,3-dioxolanes, ortho
esters, phenyl group and pentaaminocobalt(lll) complex.
Stannyl Esters
Examples of stannyl esters include triethylstannyi and tri-n-butylstannyl.
AMIDES AND HYDRAZIDES
Amides
Examples of amides include N,N-dimethyl, pyrrolidinyl, piperidinyl, 5,6-
dihydrophenanthridinyl, o-nitroanilides, N-7-nitroindolyl, N-8-Nitro-1,2,3,4-
tetrahydroquinolyl, and p-P-benzenesulfonamides.
Hydrazides
Examples of hydrazides include N-phenyl and N,N'-diisopropyl
hydrazides.

C. Synthesis
The compounds of the present invention may be prepared by
conventional synthetic organic chemistry and by matrix or combinatorial
methods according to Schemes 1 to 12 below, and Examples 1 to 13. Those
of ordinary skill in the art will be able to modify and adapt the guidance
provided herein to make the disclosed compounds.














D. Formulation and Administration
The present compounds inhibit the proteolytic activity of human
cathepsin S and therefore are useful as a medicine especially in methods for
treating patients suffering from disorders or conditions which are modulated or
regulated by the inhibition of cathepsin S activity.
The invention features a method for treating a subject with a condition
mediated by cathepsin S, said method comprising administering to the subject
a therapeutically effective amount of a pharmaceutical composition comprising
a compound of the invention. The invention also provides a method for
inhibitinq cathepsin S activity in a subject, wherein the method comprises
administering to the subject a therapeutically effective amount of a
pharmaceutical composition comprising a compound of the invention. A third
method is a method for treating an autoimmune disease, or inhibiting the
progression of an autoimmune disease, in a subject, said method comprising
administering to the subject a therapeutically effective amount of a
pharmaceutical composition comprising a disclosed compound. The
autoimmune disease can be, for example, lupus, rheumatoid arthritis, or
preferably, asthma. The invention also provides a method for treating or
inhibiting the progression of tissue transplant rejection in a subject, the method
comprising administering to the subject a therapeutically effective amount of a
pharmaceutical composition comprising a compound of the invention. The
administration step can occur before, during, and/or after a tissue transplant
procedure.
In view of their inhibitory effect on the proteolytic activity of human
cathepsin, S the compounds of the present invention may be formulated into
various pharmaceutical forms for administration purposes. To prepare these
pharmaceutical compositions, an effective amount of a particular compound, in
base or acid addition salt form, as the active ingredient is intimately mixed with
a pharmaceutically acceptable carrier.

A carrier may take a wide variety of forms depending on the form of
preparation desired for administration. These pharmaceu compositions are
desirably in unitary dosage form suitable, preferably, for our administration or
parenteral injection. For example, in preparing the compositions in oral dosage
form, any of the usual pharmaceutical media may be employed. These include
water, glycols, oils, alcohols and the like in the case of oral liquid preparations
such as suspensions, syrups, elixirs and solutions; or solid carriers such as
starches, sugars, kaolin, lubricants, binders, disintegrating agents and the like
in the case of powders, pills, capsules and tablets. In view of their ease in
administration, tablets and capsules represent the most advantageous oral
dosage unit form, in which case solid pharmaceutical carriers are generally
employed. For parenteral compositions, the carrier will usually comprise sterile
water, at least in large part, though other ingredients, for example, to aid
solubility, may be included. Injectable solutions, for example, may be prepared
in which the carrier comprises saline solution, glucose solution or a mixture of
saline and glucose solution. Injectable suspensions may also be prepared in
which case appropriate liquid carriers, suspending agents and the like may be
employed. In the compositions suitable for percutaneous administration, the
carrier optionally comprises a penetration enhancing agent and/or a suitable
wetting agent, optionally combined with suitable additives of any nature in
minor proportions, which additives do not cause a significant deleterious effect
to the skin. Such additives may facilitate the administration to the skin and/or
may be helpful for preparing the desired compositions. These compositions
may be administered in various ways, e.g., as a transdermal patch, as a spot-
on, as an ointment. Acid addition salts of the compounds of formula I, due to
their increased water solubility over the corresponding base form, are more
suitable in the preparation of aqueous compositions.
It is especially advantageous to formulate the aforementioned
pharmaceutical compositions in dosage unit form for ease of administration
and uniformity of dosage. Dosage unit form as used in the specification herein
refers to physically discrete units suitable as unitary dosages, each unit
containing a predetermined quantity of active ingredient calculated to produce

the desired therapeutic effect in association with the required pharmaceutical
carrier. Examples of such dosage unit forms are tablets (including scored or
coated tablets), capsules, pills, powder packets, waters, injectable solutions or
suspensions, teaspoonfuls, tablespoonfuls and the like, and segregated
multiples thereof.
Pharmaceutically acceptable acid addition salts include the therapeu-
tically active non-toxic acid addition salt forms which the disclosed compounds
are able to form. The latter can conveniently be obtained by treating the base
form with an appropriate acid. Appropriate acids comprise, for example,
inorganic acids such as hydrohalic acids, e.g. hydrochloric or hydrobromic
acid; sulfuric; nitric; phosphoric and the like acids; or organic acids such as, for
example, acetic, propanoic, hydroxyacetic, lactic, pyruvic, oxalic, malonic,
succinic, maleic, fumaric, male, tartaric, citric, methanesulfonic,
ethanesulfonic, benzenesulfonic, p-toluenesulfonic, cyclamic, salicylic,
p-aminosalicylic, palmoic and the like acids. The term addition salt also
comprises the solvates which the disclosed componds, as well as the salts
thereof, are able to form. Such solvates are for example hydrates, alcoholates
and the like. Conversely the salt form can be converted by treatment with alkali
into the free base form.
Stereoisomeric forms defines all the possible isomeric forms which the
compounds of formula (I) may possess. Unless otherwise mentioned or
indicated, the chemical designation of compounds denotes the mixture of all
possible stereochemically isomeric forms, said mixtures containing all
diastereomers and enantiomers of the basic molecular structure. More in
particular, stereogenic centers may have the (R)- or (S)-configuration;
substituents on bivalent cyclic saturated radicals may have either the cis- or
trans-configuration. The invention encompasses stereochemically isomeric
forms including diastereoisomers, as well as mixtures thereof in any proportion
of the disclosed compounds. The disclosed compounds may also exist in their
tautomeric forms. Such forms although not explicitly indicated in the above

and following formulae are intended to be included within the scope of the
present invention.
Those of skill in the treatment of disorders or conditions mediated by the
cathepsin S enzyme could easily determine the effective daily amount from the
test results presented hereinafter and other information. In general it is
contemplated that a therapeutically effective dose would be from 0.001 mg/kg
to 5 mg/kg body weight, more preferably from 0.01 mg/kg to 0.5 mg/kg body
weight. It may be appropriate to administer the therapeutically effective dose
as two, three, four or more sub-doses at appropriate intervals throughout the
day. Said sub-doses may be formulated as unit dosage forms, for example,
containing 0.05 mg to 250 mg, and in particular 0.5 to 50 mg of active
ingredient per unit dosage form. Examples include 2 mg, 4 mg, 7 mg, 10 mg,
15 mg, 25 mg, and 35 mg dosage forms. Compounds of the invention may
also be prepared in time-release or subcutaneous or transdermal patch
formulations. Disclosed compound may also be formulated as a spray or other
topical or inhalabie formulations.
The exact dosage and frequency of administration depends on the
particular compound of formula (I) used, the particular condition being treated,
the severity of the condition being treated, the age, weight and general
physical condition of the particular patient as well as other medication the
patient may be taking, as is well known to those skilled in the art. Furthermore,
it is evident that said effective daily amount may be lowered or increased
depending on the response of the treated patient and/or depending on the
evaluation of the physician prescribing the compounds of the instant invention.
The effective daily amount ranges mentioned herein are therefore only
guidelines.
The next section includes detailed information relating to the
preparation, characterization, and use of the disclosed compounds.


1-{4-{5-Chloro-1H-indol-3-yl)-piperidin-1-yl]-3-[5-methanesutfonyl-3-(4-
trifluoromethyl-phenyl),5,6,7-tetrahydro-pyrazolo[4,3-c]pyrldin-1-
ol.
A. 1-Methanesulfonyl-piperidin-4-one.
Potassium carbonate (324 g, 2340 mmol) was added to a solution of 4-
piperidone monohydrate hydrochloride (90 g, 586 mmol) in chloroform (300
mL) and water (300 mL). The slurry was cooled to 0 °C and treated with
methylsulfonyl chloride (136 mL, 1760 mmol) by dropwise addition over a 1 h
period (gas evolution was observed). The reaction mixture was allowed to
shake for 72 h and was partitioned between CH2CI2 (500 mL) and saturated
aqueous NaHCO3 (500 mL). The aqueous layer was extracted with CH2CI2 (3
X 200 mL). The organic layer was washed with 1 % KHSO4 (250 mL), dried
(Na2SO4), and concentrated to afford 90.5 g (87%) of a white solid. MS
(electrospray): exact mass calculated for C6H11NO3S, 177.1; m/z found, 178.1
[M+H]+, HPLC (reverse phase conditions): tR = 2.19 min. 1H NMR (400 MHz,
CDCI3): 3.60 (t, J - 6.5 Hz, 4H), 2.89 (s, 3H), 2.59 (t, J = 6.3 Hz, 4H).
B. 5-Methanesulfonyl-3-(4-trifluoromethyl-phenyl)-4,5,6,7-tetrahydro-1H-
pvrazolo[4,3-c]pyridine.
p-Toluenesulfonic acid (1.34 g, 7.0 mmol) and morpholine (25.83 mL, 296
mmol) were added to a solution of 1-methanesulfonyl-piperidin-4-one (50.0 g,
282 mmol) in benzene (282 mL). The reaction mixture was heated in a flask

equipped with a condenser and a Dean-Stark trap at reflux for 15 h. The
reaction mixture was cooled and concentrated in vacuo to give the enamine
which was used without further purification. The enamine was dissolved in
CH2CI2 (200 mL) and cooled to 0°C. To this was added triethylamine (47.2 mL,
339 mmol) followed by dropwise addition of 4-trifluoromethylbenzoyl chloride
(42.3 mL, 285 mmol) dissolved in CH2CI2 (82 mL). The reaction mixture was
allowed to warm to room temperature and stirred for 20 h. The reaction
mixture was washed with 1 N aqueous HCI (250 mL) and the CH2CI2 layer was
separated, dried (Na2SO4), and concentrated. The resulting oil was taken up in
ethanol (300 mL) and treated with hydrazine (44.3 mL, 1.41 mol) at 0 °C. The
reaction mixture was allowed to warm to room temperature and stirred for 24 h.
The mixture was concentrated and the resulting solid was filtered with ethanol
wash and dried in vacuo to afford 70 g (72%) of 5-methanesulfonyl-3-(4-
trifluoromethyl-phenyl)-4,5,6,7-tetrahydro-1H-pyrazoto[4,3-c]pyridine as a white
solid. MS (electrospray): exact mass calculated for C14H14F3N3O2S, 345.0; m/z
found, 346.0 [M+H]+. HPLC (reverse phase conditions): tR = 6.33 min. 1H NMR
(400 MHz, CDCI3): 7.72 (s, 4H), 4.58 (s, 2H), 3.69 (t, J = 5.7 Hz, 2H), 2.99 (t, J
= 5.7 Hz, 2H), 2.92 (s, 3H).
C. 5-Methanesulfonyl-1-oxiranylmethyl-3-(4-trifluoromethyl-Dhenyl)-4,5,6,7-
tetrahydro-1H-pyrazolo[4,3-c]pyridine.
5-Methanesulfonyl-3-(4-trifluoromethyl-phenyl)-4,5,6,7-tetrahydro-1H-
pyrazolo[4,3-c]pyridine (10.0 g, 29.0 mmol) and epichlorohydrin (24 mL, 307
mmol) were set stirring in DMF (150 mL) containing Cs2CO3 (10.4 g, 31.9
mmol). After stirring at room temperature for 4 days the mixture was
evaporated, brought up in EtOAc and washed with water. The organics were
dried (MgSO4) and evaporated to give a light yellow solid. Column
chromatography (silica, 5% acetone/CH2CI2) gave 4.1g (35%) of a white solid.
TLC (silica, 5% acetone/CH2CI2): Rf = 0.28. MS (electrospray): exact mass
calculated for C17H18F3N3O3S, 401.10; m/z found. 402.1 [M+H]+. 1H NMR (400
MHz, CDCI3); 7.84 (d, J = 8.3 Hz, 2H), 7.79 (d, J = 8.3 Hz, 2H), 4.70-4.62 (m,
3H), 4.25 (d, J = 5.4 Hz, 1H), 3.90-3.70 (m, 2H), 3.47 (m, 1H), 3.10-2.9 (m,
6H), 2.65-2.60 (m,1H).

P. 4-(5-Chtoro-1H-indot-3-yl)-3,6-dihydro-2H-pyridine-1-carboxytic acid tert-
butyl ester.
5-Chloro-1H-indole (3.2 g, 20 mmol), 4-oxo-piperidine-1-carboxylic acid tert-
butyl ester (7.97 g, 40 mmol) and potassium hydroxide (4.5 g, 80 mmol) were
added in MeOH (40 mL) and heated to reflux for 16 h. The reaction mixture
was then cooled to room temperature and poured into ice water (200 mL). The
mixture were extracted with 10% MeOH/CH2CI2 (5 x 100 mL). The organic
extracts was dried over Na2SO4 and concentrated to form a solid. The solid
was washed with MeOH (100 mL), filtered and dried to give a light yellow solid
6.3 g (94%). TLC (silica, 5% MeOH/CH2CI2):Rf= 0.8. MS (electrospray):
exact mass calculated for C18H21CIN2O2, 332.12; m/z found, 355.0 [M++Na].
1H NMR (CDCI3, 400 MHz): 8.26 (br s, 1H), 7.83 (d, J = 1.76 Hz, 1H), 7.28 (d, J
= 8.80 Hz, 1H), 7.19-7.14 (m, 2H), 6.09 (br s, 1H), 4.15-4.10 (m, 2H), 3.66 (t, J
= 5.67 Hz, 2H), 2.56-2.49 (m, 2H), 1.50 (s, 9H).
E. 4-(5-Chloro-1H-indol-3-yl)-piperidine-1-carboxylic acid tert-butyl ester.
4-(5-Chloro-1H-indol-3-yl)-3,6-dihydro-2H-pyridine-1-carboxylic acid tert-butyl
ester (6.3 g, 18.9 mmol) in EtOH (125 mL) containing PtO2 (1 g) was placed on
a Parr hydrogenator at 60 psi H2. After 18 h the mixture was filtered through
celite and evaporated to give a white solid 6.0 g (94%). TLC (silica, 5%
MeOH/CH2CI2): Rt = 0.8. MS (electrospray): exact mass calculated for
C18H23CIN2O2, 334.14; m/z found, 335.1 [M++H]. 1H NMR (CDCI3,400 MHz)
8.46 (br s, 1H), 7.51 (d, J - 8.41 Hz, 1H), 7.32 (d, J = 1.57 Hz, 1H), 7.06 (dd, J
= 6.46 Hz, 2.15 Hz, 1H), 6.92 (d, J = 2.35 Hz, 1H), 4.24 (d, J = 13.11 Hz, 2H),
2.98-2.84 (m, 3H), 2.00 (d, J = 12.72 Hz, 2H), 1.69-1.55 (m, 2H), 1.50 (s. 9H).
F. 5-Chloro-3-Diperidin-4-yl-1H-indole.
4-(5-Chloro-1H-indol-3-yl)-piperidine-1-carboxylic acid tert-butyl ester (3.4 g,
10.2 mmol) was set stirring in 1:1 TFA/CH2CI2. After 45 min the mixture was
evaporated and the golden oil brought up in Et2O. A solid formed and was
filtered, washed with Et2O and air dried to give 3.5 g (97%) of a white solid as a

TFA salt. MS (electrospray): exact mass calculated for C12H15CIN2, 234.09; m/z
found, 235.1 [M++H].
G. 1-[4-(5-Chlorp-1H-indol-3-yl)-piperidin-1-vl]-3-[5-methanesulfonyl-3-(4-
trifluoromethyl-phenyl)-4,5,6,7-tetrahydro-pyrazolo[4,3-c]pyridin-1-yl)-propan-2-
ol.
5-Chloro-3-piperidin-4-yl-1H-indole (350 mg, 1.00 mmol) and 5-methane-
sulfonyl-1-oxiranylmethyl-3-(4-trifluoromethyl-phenyl)-4,5,6,7-tetrahydro-1H-
pyfazolo[4,3-c]pyridine (401 mg, 1.00 mmol) were set stirring in EtOH (20 mL)
containing Et3N (215 ?L, 1.54 mmol) at 80 °C. After 16 h the mixture was
cooled, evaporated, brought up in CH2CI2 and washed with water. The
organics were dried over Na2SO4 and concentrated. Column chromatography
(silica, 0-10% MeOH/CH2CI2) provided 551 mg (88%) of a white solid. TLC
(silica, 10% MeOH/CH2CI2): Rf= 0.8. MS (electrospray): exact mass calculated
for C30H33CIF3N5O3S, 635.19; m/z found, 636.2 [M++H]. 1H NMR (CDCI3, 400
MHz): 8.82 (br s, 1H), 7.68 (d, J = 8.41 Hz, 2H), 7.61 (d, J = 8.6 Hz, 2H), 7.54
(br s, 1H), 7.16 (d, J - 8.41 Hz, 1H), 7.03 (dd, J - 7.0 Hz, 1.6 Hz, 1H), 6.85 (br
s, 1H), 4.43 (dd, J- 25.2 Hz, 14.6 Hz, 2H), 4.30-4.05 (m, 3H), 4.00-3.88 (m,
1H), 3.62-3.50 (m, 1H), 3.47-3.35 (m, 1H), 3.02-2.89 (m, 2H), 2.88-2.81 (m,
2H), 2.79 (s, 3H), 2.72-2.60 (m, 1H), 2.47-2.28 (m, 3H), 2.12-2.00 (m, 1H),
1.96-1.85 (m, 2H), 1.74-1.50 (m, 2H).

1-[4-(7-Chloro-1H-indol-3-yl)-piperidin-1-yl]-3-[5-methanesulfonyl-3-(4-
trifluoromethyl-phenyl)-4,5,6,7-tetrahydro-pyrazolo[4,3-c]pyridin-1-yl]-propan-2-
ol.

A. 4-[7-Chloro-1H-indol-2-yl)-3,6-dihydro-2H-pyridine-1-carboxylicacid tert-
butyl ester.
7-Chloro-1H-indole (3.2g, 20 mmol), 4-oxo-piperidine-1-carboxylic acid tert-
butyl ester (7.97 g, 40 mmol) and potassium hydroxide (4.5 g, 80 mmol) were
added in MeOH (40 mL) and heated to reflux for 16 h. The reaction mixture
was then cooled to room temperature and poured into ice water (200 mL). The
mixture was extracted with 10% MeOH/CH2CI2 (5 x 100 mL). The organic
extracts was dried over Na2SO4 and concentrated to form a solid. The solid
was washed with MeOH (100 mL), filtered and dried to give a light yellow solid
6.3 g (94%). TLC (silica, 5% MeOH/CH2CI2): R,= 0.8. MS (electrospray):
exact mass calculated forC18H21CIN2O2, 332.12; m/z found, 355.0 [M++Na].
1H NMR (CDCl3 400 MHz): 8.26 (br s, 1H), 7.83 (d, J = 1.76 Hz, 1H), 7.28 (d, J
= 8.80 Hz, 1H), 7.19-7.14 (m, 2H), 6.09 (br s, 1H), 4.15-4.10 (m, 2H), 3.66 (t, J
- 5.67 Hz, 2H), 2.56-2.49 (m, 2H), 1.50 (s, 9H).
B. 4-(7-Chloro-1H-indol-3-yl)-piperidine-1-carboxylic acid tert-butyt ester.
4-(7-Chloro-1H-indol-3-yl)-3,6-dihydro-2H-pyridine-1-carboxylic acid tert-butyl
ester (6.3 g, 18.9 mmol) in EtOH (125 mL) containing PtO2 (1 g) was placed on
a Parr hydrogenator at 60 psi H2. After 18 h the mixture was filtered through
celite and evaporated to give a white solid 6.0 g (94%). TLC (silica, 5%
MeOH/CH2CI2): R, = 0.8. MS (electrospray): exact mass calculated for
C18H23ClN2O2, 334.14; m/z found, 335.1 [M++H]. 1H NMR (CDCI3, 400 MHz):
8.46 (br s, 1H), 7.51 (d, J = 8.41 Hz, 1H), 7.32 (d, J= 1.57 Hz, 1H), 7.06 (dd, J
= 6.46 Hz, 2.15 Hz, 1H), 6.92 (d, J = 2.35 Hz, 1H). 4.24 (d. J- 13.11 Hz. 2H),
2.98-2.84 (m, 3H), 2.00 (d, J - 12.72 Hz, 2H), 1.69-1.55 (m, 2H), 1.50 (s, 9H).
C. 7-Chloro-3-piperidin-4-yl-1H-indole.
4-(7-Chloro-1H-indol-3-yl)-piperidine-1-carboxylic add tert-butyl ester (3.4 g,
10.2 mmol) was set stirring in 1:1 TFA/CH2CI2. After 45 min the mixture was
evaporated and the golden oil brought up in Et2O. A solid formed and was
filtered, washed with Et2O and air dried to give 3.5 g (97%) of a white solid.

MS (electrospray): exact mass calculated for C12H1SCIN2,234.09; m/z found,
235.1 [M++H].
D. 1-[4-(7-Chloro-1H-indol-3-yl)-piperidin-1-yl]-3-[5-methanesulfonyl-3-(4-
trffluoromethvl-phenyl)-4,5,6,7-tetrahydro-pyrazollo[4,3-c]pyridin-1-yl]-propan-2-
ol.
7-Chloro-3-piperidin-4-yl-1H-indole (341 mg, 0.97 mmol) and 5-methane-
sulfonyl-1-oxiranylmethy1-3-(4-trifluoromethyl-phenyl)-4,5,6,7-tetrahydro-1H-
pyrazolo[4,3-c]pyridine (130 mg, 0.32 mmol) were set stirring in EtOH (15 mL)
containing Et3N (135 ?L, 0.97 mmol) at 80 °C. After 16 h the mixture was
cooled, evaporated, brought up in CH2CI2 and washed with water. The
organics were dried over Na2SO4 and concentrated. Column chromatography
(silica, 0-10% MeOH/CH2CI2) gave 120 mg (65%) of a white solid. TLC (silica,
10% MeOH/CH2CI2): R, = 0.7. MS (electrospray): exact mass calculated for
C30H33CIF3N5O3S, 635.19; m/z found, 636.2 [M++H]. 1H NMR (CDCI3, 400
MHz): 8.55 (br s, 1H), 7.70 (d, J = 8.22 Hz, 2H), 7.63 (d, J = 8.4 Hz, 2H), 7.49
(d, J - 9.4 Hz, 1H), 7.14 (d, J = 7.8 Hz, 1H), 7.00 (t, J = 8.02 Hz, 1H), 6.94 (br
s, 1H), 4.51 (dd, J = 12.5 Hz, 14.5 Hz, 2H), 4.25-4.11 (m, 3H), 4.07-3.95 (m,
1H), 3.73-3.61 (m, 1H), 3.61-3.50 (m, 1H), 3.11-2.98 (m, 2H), 2.88-2.85 (m,
2H), 2.83 (s, 3H), 2.82-2.72 (m, 1H), 2.55-2.38 (m, 3H), 2.24-2.10 (m, 1H),
2.05-1.90 (m, 2H), 1.82-1.61 (m, 2H).

1 -[4-(5-Chloro-2-methyl-1H-indol-3-yl)-piperidin-1-yl]-3-[5-methanesulfonyl-3-(4-
trifluoromethyl-phenyl)-4,5,6,7-tetrahydro-pyrazolo[4,3-c]pyridin-1-yl]-propan-2-
ol.

A. 4-[5-Chloro-2-methyl-1H-indol-3-yl)-3,6-dihydro-2H-pyridine-1-carboxylic
acid tert-butyl ester.
5-Chtoro-2-methyl-1H-indole (3.3 g, 20 mmol), 4-oxo-piperidine-1-carboxylic
acid tert-butyl ester (7.97 g, 40 mmol) and potassium hydroxide (4.5 g, 80
mmol) were added in MeOH (40 mL) and heated to reflux for 16 h. The
reaction mixture was then cooled to room temperature and poured into ice
water (200 mL). The mixture was extracted with 10% MeOH/CH2CI2 (5 x 100
mL). The organic extracts was dried over Na2SO4 and concentrated to form a
solid. The solid was washed with MeOH (100 mL), filtered and dried to give a
light yellow solid 6.2 g (90%). TLC (silica, 5% MeOH/CH2CI2): Rf = 0.8.
MS (electrospray): exact mass calculated for C19H23CIN2O2, 346.14; m/z found,
347.1 [M++H].
B. 4-[5-Chloro-2-methyl-1H-indol-3-yl)-piperidine-1-carboxylic acid tert-butyl
ester.
4-(5-Chloro-2-methyl-1H-indol-3-yl)-3,6-dihydro-2H-pyridine-1-carboxylic acid
tert-butyl ester (6.2 g, 17.9 mmol) in EtOH (125 mL) containing PtO2 (1 g) was
placed on a Parr hydrogenator at 60 psi H2. After 18 h the mixture was filtered
through celite and evaporated to give a white solid 6.2 g (99%). TLC (silica,
5% MeOH/CH2Cl2): Rf = 0.8. MS (electrospray): exact mass calculated for
C19H25CIN2O2, 348.16; m/z found, 349.1 [M++H].
C. 5-Chloro-2-methyl-3-piperidin-4-yl-1H-indole.
4-(5-Chloro-2-methyl-1H-indol-3-yl)-piperidine-1-carboxylic acid tert-butyl ester
(6.2 g, 107.8 mmol) was set stirring in 1:1 TFA/CH2CI2. After 45 min the
mixture was evaporated and the golden oil brought up in Et2O. A solid formed
and was filtered, washed with Et2O and air dried to give 6.2 g (95%) of a white
solid as a TFA salt. MS (electrospray): exact mass calculated for C14H17CIN2,
248.11; m/z found, 249.1 [M++H].

P. 1 -[4-(5-Chloro-2-methyl-1H-indol-3-yl)-piperidin-1-yl]-3-[5-methanesulfonyl-
3-(4-trifluoromethyl-phenyl)-4,5,6,7-tetrahydro-pyrazolo[4,3-c]pyridin-1-yl]-
propan-2-ol.
5-Chloro-2-methyl-3-piperidin-4-yl-1H-indole (480 mg, 1.32 mmol) and 5-
methanesulfonyl-1-oxiranylmethyl-3-(4-trifluoromethyl-phenyl)-4,5,6,7-
tetrahydro-1H-pyrazolo[4,3-c]pyridine (177 mg, 0.44 mmol) were set stirring in
EtOH (20 mL) containing Et3N (215 ?L, 1.54 mmol) at 80 °C. After 16 h the
mixture was cooled, evaporated, brought up in CH2CI2 and washed with water.
The organics were dried over Na2SO4, and concentrated. Column
chromatography (silica, 0-10% MeOH/CH2CI2) gave 169 mg (62%) of a white
solid. TLC (silica, 10% MeOH/CH2CI2):R,= 0.6. MS (etectrospray): exact
mass calculated for C31H35CIF3N5O3S, 649.21; m/z found, 650.2 [M++H]. 1H
NMR (CDCl3, 400 MHz): 8.00 (s, 1H), 7.70 (d, J = 8.11 Hz, 2H), 7.64 (d, J =
8.41 Hz, 2H), 7.57 (d, J - 1.96 Hz, 1H), 7.12 (d, J = 8.61 Hz, 1H), 6.99 (dd, J =
6.85 Hz, 1.96 Hz, 1H), 4.53 (dd, J = 14.28 Hz, 12.91 Hz, 2H), 4.26-4.14 (m,
2H), 4.09-3.99 (m. 1H), 3.75-3.65 (m, 1H), 3.64-3.54 (m, 1H), 3.14-3.02(m,
2H), 3.00-2.89 (m, 2H), 2.86 (s, 3H), 2.76-2.63 (m, 1H), 2.54-2.45 (m, 2H),
2.45-2.36 (m, 1H), 2.34 (s, 3H), 2.25-2.00 (m, 3H), 1.77-1.63 (m, 2H).

1-{4-[6-Chloro-1-(2-morpholin-4-yl-ethyl)-1H-indol-3-yl]-piperidin-1-yl}-3-[5-
rnethanesulfonyl-3-(4-trifluoromethyl-phenyl)-4,5,6,7-tetrahydro-pyrazolo[4,3-
c]pyridin-1-yl]-propan-2-ol.

A. 6-Chloro-3-piperidin-4-yl-1H-indole.
6-Chloro-1H-indole (3.2g, 20 mmol), piperidin-4-one monohydrate (6.1 g, 40
mmol) and potassium hydroxide (4.5 g, 80 mmol) were added in MeOH (40
mL) and heated to reflux for 16 h. The reaction mixture was then cooled to
room temperature and poured into ice water (200 mL). The mixture was
extracted with 10% MeOH/CH2Cl2 (5 x 100 mL). The organic extracts were
dried over Na2SO4 and concentrated. Column chromatography (silica, 20-
100% MeOH/CH2CI2with 2% NH4OH) to obtain 5.8 9 (100%) of a yellow solid.
The solid (5.8 g, 20 mmol) in EtOH (150 mL) containing PtO2 (1 g) was placed
on a Parr hydrogenator at 60 psi H2. After 18 h the mixture was filtered through
cellte and evaporated to give an off white solid 4.6 g (97%). MS (electrospray):
exact mass calculated for C13H15CIN2, 234.09; m/z found, 235.0 [M++H].
B. 4-(6-Chloro-1H-indol-3-yl-piperidine-1-carboxylic acid tert-butyl ester.
To a solution of 6-chloro-3-piperidin-4-yl-1H-indole (4.6 g, 19.5 mmol) in DMF
(20 mL) was added di-tert-butyl dicarbonate (4.6 g, 21.4 mmol). The reaction
mixture was stirred at room temperature for 6 h. The reaction mixture was
dissolved in EtOAc (400 mL). washed with water (3 x 50 mL), brine (1 x 50
mL). The organic layer was dried over Na2SO4 and concentrated. Column
chromatography (silica, 20-50% EtOAc/hexanes) gave 4.2 g (64%) of the
desired product TLC (silica, 20% EtOAc/hexanes): Rf = 0.24. MS
(electrospray): exact mass calculated for C18H23CIN2O2, 334.14; m/z found,
335.1 [M++H]. 1H NMR (CDCI3, 400 MHz) 8.46 (br s, 1H), 7.42 (d, J = 8.61 Hz,
1H), 7.14 (d, J = 1.57 Hz, 1H), 6.96 (dd, J - 6.65 Hz, 1.76 Hz, 1H), 6.74 (s,
1H), 4.14 (br s, 2H), 2.89-2.70 (m, 3H), 1.90 (d, J = 12.13, 2H), 1.65-1.50 (m,
2H),1.41 (s,9H).
C. 4-[6-Chloro-1-(2-morpholin-4-yl-ethyl)-1H-indol-3-yl]-piperidine-1-carboxylic
acid tert-butyt ester.
4-(6-Chloro-1H-indol-3-yl)-piperidine-1-carboxylic acid tert-butyl ester (2.0 g,
5.95 mmol) was dissolved in THF (30 mL). At 0 °C, potassium
bis(trimethylsilyl)amide (2.37 g, 11.9 mmol) was added. The reaction mixture
was stirred at room temperature for 1 h. 4-(2-Chloro-ethyl)-morpholine

hydrochtoride (1.8 g, 11.9 mmol) was added and stirred at room temperature
for an additional 1 h. The mixture was dissolved in EtOAC (250 mL) and
washed with water (2 x 30 mL) and brine (30 mL). The organics were dried
over Na2SO4 and concentrated. Column chromatography (silica, 0-5%
MeOH/CH2CI2) provided 2.6 g (97%) of a white solid. TLC (silica, 5%
MeOH/CH2CI2): Rf= 0.67. MS (elecrospray): exact mass calculated for
C24H34CIN3O3, 447.23; m/z found, 448.2 [M++H]. 1H NMR (CDCI3, 400 MHz):
7.45 (d, J = 8.61 Hz, 1H), 7.27 (d, J = 1.57 Hz, 1H), 6.99 (dd, J = 6.65 Hz, 1.76
Hz, 1H), 6.84 (s, 1H), 4.18 (br s, 2H), 4.06 (t, J - 6.85 Hz, 2H), 3.69-3.60 (m,
4H), 2.92-2.80 (m, 2H), 2.69-2.60 (m, 3H), 2.44 (t J = 4.89 Hz, 2H), 2.40 (t, J =
4.30 Hz, 2H), 1.94 (d, J = 12.13, 2H), 1.65-1.50 (m, 2H), 1.45 (s, 9H).
P. 6-Chloro-1-(2-morpholin-4-yl-ethyl)-3-piperidin-4-yl-1H-indole.
4-[6-Chloro-1-(2-morpholin-4-yl-ethyl)-1H-indol-3-yl]-piperidine-1-carboxylic
acid tert-butyl ester (2.6 g, 5.81 mmol) was set stirring in 1:1 TFA/CH2CI2. After
45 min the mixture was evaporated and the golden oil brought up in Et2O. A
solid formed and was filtered, washed with Et2O and air dried to give 2.5 g
(95%) of a white solid. MS (electrospray): exact mass calculated for
C19H26CIN3O, 347.18; m/z found, 348.2 [M++H].
E. 1-[4-[6-Chloro-1-(2-morpholin-4-yl-ethyn-1H-indol-3-yl]-piperidin-1-yl}-3-[5-
methanesulfonyl-3-(4-trifluoromethyl-phenyl)-4,5,6,7-tetrahydro-pyrazolo[4,3-
c]pyridin-1-yl]-propan-2-ol.
6-Chloro-1-(2-morpholin-4-yl-ethyl)-3-piperidin-4-yl-1H-indole (209 mg, 0.6
mmol) and 5-methanesulfonyl-1-oxiranylmethyl-3-(4-trifluoromethyl-phenyl)-
4,5,6,7-tetrahydro-1H-pyrazolo[4,3-c]pyridine (120 mg, 0.3 mmol) were set
stirring in EtOH (20 mL) containing Et3N (84 uL, 0.6 mmol) at 80 °C. After 16 h
the mixture was cooled, evaporated, brought up in CH2CI2 and washed with
water. The organics were dried over Na2SO4 and concentrated. Column
chromatography (silica, 0-10% MeOH/CH2CI2) provided 180 mg (85%) of a
white solid. TLC (silica, 10% MeOH/CH2CI2): Rf= 0.54. MS (electrospray):
exact mass calculated for C36H44CIF3N6O4S, 748.28; m/z found, 749.3 [M++H].
1H NMR (CDCI3, 400 MHz): 7.70 (d. J = 8.61 Hz, 2H), 7.64 (6, J = 8.261 Hz,

2H), 7.47 (d, J = 8.80 Hz, 1H), 7.29 (d, J = 1.96, 1H), 7.02 (dd, J = 6.46 Hz,
1.76 Hz, 1H), 6.81 (br s, 1H), 4.54 (dd, J = 4.09 Hz, 7.43 Hz, 2H), 4.24-4.14
(m, 2H), 4.14-4.08 (m, 2H), 4.06-3.98 (m, 1H), 3.73-3.57 (m, 5H), 3.12-3.02 (m,
2H), 2.97-2.87 (m, 2H), 2.86 (s, 3H), 2.83-2.74 (m, 1H), 2.70-2.64 (t, J = 7.24
Hz, 2H), 2.54-2.42 (m, 8H), 2.23-2.14 (m, 1H), 2.05-1.96 (m, 2H). 1.82-1.60 (m,
2H).

1-[5-Methanesutfonyl-3-(4-trifluoromethyl-phenyl)-4,5,6,7-tetrahydro-
pyrazolo[4,3-c]pyridin-1-yl]-3-[4-(1H-pyrrolo[3,2-c]pyridin-3-yl)-piperidin-1-yl]-
propan-2-ol.
A. 4-(1H-Pyrrolo[3,2-c]pyridin-3-yl)-3,6-dihydro-2H-pyridine-1-carboxylic acid
tert-butyl ester.
A solution of 1.9 g (8.47 mmol) of 1H-pyrrolo[3,2-c]pyridine (synthesized
following the procedure described in Synthesis, 1996, 882), 4-oxo-piperidine-1-
carboxylic acid tert-butyl ester (3.4 g, 16.9 mmol) and potassium hydroxide (1.9
g, 33.9 mmol) in MeOH (20 mL) was heated to reflux for 16 h. The reaction
mixture was then cooled to room temperature and poured into ice water (100
ml). The mixture was extracted with 10% MeOH/CH2CI2 (5 x 50 mL). The
organic extracts was dried over Na2SO4 and concentrated to form a solid. The
solid was washed with MeOH (50 mL), filtered and dried to give a light yellow
solid 2.0 g (79%). TLC (silica, 10% MeOH/CH2CI2): Rf = 0.5. MS
(electrospray): exact mass calculated for C17H21N3O2, 299. 16; m/z found, 300.1
[M++H]. 1H NMR (CDCI3, 400 MHz): 12.26 (br s, 1H), 9.20 (s, 1H), 8.28 (d, J =
5.67 Hz, 1H), 7.35 (dd, J = 5.09 Hz, 0.78 Hz, 1H). 7.32 (s. 1H), 6.19 (br s, 1H),
4.14 (br s, 2H), 3.68 (t, J = 5.67 Hz, 2H), 2.61-2.55 (m, 2H), 1.48 (s, 9H).

B. 4-(1H-Pyrrolo[3,2-c]pyridin-3yl]-piperidine-1-carboxylic acid tert-butyl ester.
4-(1H-Pyrrolo[3,2-c]pyridin3-yl)-3,6-dihydro-2H-pyrldine-1-carboxylic acid tert-
butyl ester (2 g, 6.6 mmol) in EtOH (50 mL) containing PtO2 (500 mg) was
placed on a Parr hydrogenator at 60 psi H2. After 18 h the mixture was filtered
through celite and evaporated to give a white solid (2.0 g, 100%). TLC (silica,
10% MeOH/CH2CI2): Rf= 0.49. MS (electrospray): exact mass calculated for
C17H23N3O22, 301.18; m/z found, 302.2 [M++H]. 1H NMR (CDCI3, 400 MHz):
13.66 (br s, 1H), 8.88 (s, 1H), 8.79 (d, J - 6.46 Hz, 1H), 7.69 (d, J = 6.46 Hz,
1H), 7.30 (s, 1H), 4.14 (br s, 2H), 2.99-2.87 (m, 1H), 2.86-2.71 (m, 2H), 1.91 (d,
J = 11.54 Hz, 2H), 1.64-1.50 (m, 2H), 1.38 (s, 9H).
C. 3-Piperidin-4-yl-1H-pyrrolo[3,2-c]pyridine.
4-(1H-Pyrrolo[3,2-c]pyridin-3-yl)-piperidine-1-carboxylic acid tert-butyl ester (2.0
g, 6.6 mmol) was set stirring in 1:1 TFA/CH2CI2. After 45 min the mixture was
evaporated and the golden oil brought up in Et2O. A solid formed and was
filtered, washed with Et2O and air dried to give 2.1 g (100%) of a white solid as
a TFA salt MS (electrospray): exact mass calculated for C12H15N3,201.13; m/z
found, 202.1 [M++H]. 1H NMR (CDCI3, 400 MHz): 9.4 (br s, 1H), 8.96 (s, 1H),
8.26 (d, J - 5.87 Hz, 1H), 7.24 (s, 1H), 6.99 (s, 1H), 3.22-3.16 (m, 2H), 3.05-
2.95 (m, 1H), 2.86-2.77 (m, 2H), 2.05 (d, J = 12.72 Hz, 2H), 1.89 (br s, 1H),
1.75-1.63 (m, 2H).
D. 1-[5-Methanesulfonyl-3-(4-trifluoromethyl-phenyl)-4,5,6,7-tetrahydro-
pyrazolo[4,3-c]pyridin-1-yl]-3-[4-(1H-pyrrolo[3,2-c)pyridin-3-yl)-piperilin-1-vl]-
propan-2-ol.
3-Piperidin-4-yl-1H-pyrrolo[3,2-c]pyridine (159 mg, 0.5 mmol) and 5-
methanesulfonyl-1-oxiranylmethyi-3-(4-trifluoromethyl-phenyl)-4,5,6,7-
tetrahydro-1H-pyrazolo[4,3-c]pyridine (200 mg, 0.5 mmol) were set stirring in
EtOH (10 mL) containing Et3N (112 uL, 0.77 mmol) at 80 °C. After 16 h the
mixture was cooled, evaporated, brought up in CH2CI2 and washed with water.
The organics were dried over Na2SO4 and concentrated. Column
chromatography (silica, 0-10% (2 N NH3 in MeOH)/CH2CI2) provided 82 mg

(27%) of a white solid. TLC(silica, 10% MeOH/CH2Cl2):R,=0.8. MS
(electrospray): exact mass calculated for C29H33F3N6O3S, 602.23; m/z found,
603.2 [M++H]. 1H NMR (CDCI3, 400 MHz): 9.62 (s, 1H), 8.90 (s. 1H), 8.21 (d, J
= 5.87 Hz, 1H), 7.69 (d, J = 7.83 Hz, 2H), 7.62 (d, J = 8.41 Hz, 2H), 7.23 (d, J =
5.87, 1H), 6.97 (s. 1H), 4.51 (dd, J = 14.48 Hz, 8.80 Hz, 2H), 4.23-4.13 (m,
2H), 4.05-3.95 (m, 1H). 3.72-3.54 (m, 3H), 3.11-2.98 (m, 2H), 2.95-2.86 (m,
2H), 2.84 (s, 3H), 2.51-2.39 (m, 3H), 2.20-2.11 (m, 1H), 2.07-1.97 (m, 2H),
1.85-1.63 (m,2H).

1-[5-Methanesulfonyl-3-(4-trifluoromethyl-phenyl)-4,5,6,7-tetrahydro-
pyrazoto[4,3-c]pyridin-1-yl]-3-[4-(1H-pyrrolo[2,3-b]pyridin-3-yl)-piperidin-1-yl]-
propan-2-ol.
A. 4-(1H-Pyrrolo[2,3-b]pyridin-3-yl)-3,6-dihydro-2H-pyridine-1-carboxylic acid
tert-butyt ester.
1H-Pyrrolo[2,3-b]pyridine (3 g, 25 mmol), 4-oxo-piperidine-1-carboxylic acid
tert-butyl ester (4.2 g, 21 mmol) and potassium hydroxide (3.56 g, 63 mmol)
were added in MeOH (60 mL) and heated to reflux for 16 h. The reaction
mixture was then cooled to room temperature and poured into ice water (300
mL). The mixture was extracted with 10% MeOH/CH2CI2 (5 x 150 mL). The
organic extracts was dried over Na2SO4 and concentrated to form a solid. The
solid was washed with MeOH (150 mL), filtered and dried to give a light yellow
solid 5.7 g (91%). TLC (silica, 50% EtOAc/hexanes): Rf = 0.3. MS
(electrospray): exact mass calculated for C17H21N3O2, 299.16; m/z found, 300.2
[M++H]. 1H NMR (CDCI3, 400 MHz) 10.97 (br s, 1H), 8.33 (dd, J = 3.33 Hz,
1.37 Hz, 1H), 8.20 (dd, J = 6.65 Hz, 1.37 Hz, 1H), 7.34 (br s, 1H), 7.25 (s, 1H).

7.13 (dd, J = 4.89 Hz, 3.13 Hz, 1H), 4.14 (br s, 2H), 3.68 (t, J = 5.28 Hz, 2H),
2.56 (brs, 2H). 1.49 (s. 9H).
B. 4-(1H-Pyrrolo[2,3-b]pyridin-3-yl)-piperidine-1-carboxylic acid tert-butyl ester.
4-(1H-Pyrrolo[2,3-b]pyridin-3-yl)-3,6-dihydro-2H-pyridine-1-carboxylic acid tert-
butyl ester (1 g, 3.3 mmol) in EtOH (25 mL) containing PtO2 (250 mg) was
placed on a Parr hydrogenator at 60 psi H2. After 18 h the mixture was filtered
through celite and evaporated to give 0.96 g (97%) of a white solid. TLC
(silica, 50% EtOAc/hexanes): Rf = 0.5. MS (electrospray): exact mass
calculated for C17H23N3O22, 301.18; m/z found, 302.2 [M++H]. 1H NMR (CDCI3,
400 MHz) 10.95 (brs, 1H), 8.26 (dd, J = 3.33 Hz, 1.37 Hz, 1H), 7.96 (dd, J =
6.26 Hz, 1.57 Hz, 1H), 7.11 (s, 1H), 7.05 (dd, J = 4.89 Hz, 3.13 Hz, 1H), 4.22
(br s, 2H), 3.00-2.79 (m, 3H), 1.99 (d, J = 13.89 Hz, 2H), 1.74-1.60 (m, 2H),
1.47 (s, 9H).
C. 3-Piperidin-4-yl-1H-pyrrolo[2,3-b]pyridine.
4-(1H-Pyrrolo[2,3-b]pyridin-3-yl)-piperidine-1-carboxylic acid tert-butyl ester
(963 mg, 3.2 mmol) was set stirring in 1:1 TFA/CH2CI2. After 45 min the
mixture was evaporated and the golden oil brought up in Et2O. A solid formed
and was filtered, washed with Et2O and air dried to give 974 mg (96%) of a
white solid as a TFA salt MS (electrospray): exact mass calculated for
C12H15N3, 201.13; m/z found, 202.1 [M++H]. 1H NMR (CDCI3, 400 MHz): 8.09
(dd, J = 3.33 Hz, 1.57 Hz, 1H), 7.89 (dd, J = 6.26 Hz, 1.57 Hz, 1H), 7.01 (s,
1H), 6.99 (dd, J = 4.89 Hz, 3.13 Hz, 1H), 5.04 (br s, 2H), 3.11-3.04 (m, 2H),
2.88-2.79 (m, 1H), 2.73-2.64 (m, 2H), 1.94 (d, J = 12.52 Hz, 2H), 1.65-1.63 (m,
2H).
P. 1-[5-Methanesulfonyl-3-(4-trifluoromethyl-phenyl)-4,5,6,7-tetrahydro-
pyrazolo[4,3-c]pyridin-1-yl]-3-[4-(1H-pyrrolo[2,3-b]pyridin-3-yl)piperidin-1-vl]-
propan-2-ol.
3-Piperidin-4-yl-1H-pyrrolo[2,3-b]pyridine (443 mg, 1.4 mmol) and 5-
methanesulfonyl-1-oxiranylmethyl-3-(4-trifluoromethyl-phenyl)-4,5,6,7-
tetrahydro-1H-pyrazolo[4,3-c]pyridine (289 mg, 0.7 mmol) were set stirring in

EtOH (10 mL) containing Et3N (146 ?L, mmol) at 80 °C. After 16 h the mixture
was cooled, evaporated, brought up in CH2CI2 and washed with water. The
organics were dried over Na2O4, and concentrated. Column chromatography
(silica, 0-10% (2 N NH3 in MeOH)/CH2CI2) provided 107 mg (25%) of a white
solid. TLC (silica. 10% MeOH/CH2CI2): Rf= 0.45. MS (electrospray): exact
mass calculated for C29H33F3N6O3S, 602.23; m/z found. 603.3 [M++H]. 1H NMR
(CDCI3, 400 MHz): 10.6 (br s, 1H), 8.24 (m, 1H), 7.91 (m, 1H), 7.70 (m, 2H),
7.63 (m, 2H), 7.05 (br s, 1H), 7.02 (m, 1H), 4.52 (dd, J = 4.28 Hz, 9.78 Hz, 2H),
4.24-4.16 (m. 2H), 4.06-3.98 (m, 1H), 3.72-3.64 (m, 1H), 3.64-3.55 (m, 1H),
3.11-3.00 (m, 2H), 2.96-2.87 (m, 2H). 2.85 (s, 3H), 2.82-2.74 (m, 1H), 2.53-
2.40 (m, 3H), 2.22-2.12 (m, 1H), 2.05-1.95 (m, 2H), 1.85-1.64 (m, 2H).

1-[5-Methanesulfonyl-3-(4-trifluoromethyl-phenyl)-4,5,6,7-tetrahydro-
pyrazolo[4,3-c]pyridin-1-yl]-3-[4-(5-morpholin-4-yl-1H-pyrrolo[2,3-c]pyridin-3-yl)-
piperidin-1-yl]-propan-2-ol.
A. [2-(2-Chloro-5-nitro-pyridin-4-yl)-yinyl]-dimethyl-amine.
A solution of 2-chloro-4-methyl-5-nitro-pyridine (2 g, 11.59 mmol) in DMF (11.6
mL) was treated with 3.08 mL (23.2 mmol, 2 eq) of DMF-dimethylacetal and
the reaction mixture was stirred at 100 °C for 4 h. All volatiles were removed
under reduced pressure. Column chromatography (silica, 20% EtOAc/hexanes)
provided 2.37 g (90%) of [2-(2-chloro-5-nitro-pyridin-4-yl)-vinyl]-dimethyl-amine.
TLC (silica, 20% EtOAc/hexanes): Rf = 0.30. MS (electrospray): exact mass
calculated for C9H10CIN3O2, 227.05; m/z found, 228.1 [M+H]+. 1H NMR (400

MHz, CDCl3: 8.79 (s, 1H), 8.02 (s, 1H), 7.35 (d, J = 13 Hz, 1H), 5.94 (d, J = 13
Hz, 1H), 2.96 (s, 3H), 2.87 (s, 3H).
B. 5-Morpholin-4-yl-1H-pyrrolo[2,3-c]pyridine.
A solution of 450 mg (2 mmol) of [2-(2-chloro-5-nitro-pyridin-4-yl)-yinyl]-
dimethyl-amine in a 20 mL of mixed solvent of MeOH-CH2CI2 (1:1) was treated
with 3 mL of morpholine. The reaction mixture was stirred at 65 °C for 8 h.
Volatiles were then removed. CH2CI2 (100 mL) and H2O (30 mL) were added.
The organic layer was separated and washed with H2O (30 mL), brine (30 mL),
dried over Na2SO4 and concentrated. The red powder was treated with 4.0 g
(63 mmol, 32 eq) of ammonium formate and 10% Pd-C (120 mg). The reaction
mixture was stirred at 65 °C for 30 min. The reaction mixture was then filtered
through a pad of celite and concentrated to obtain a yellow solid. Column
chromatography (silica, 5% MeOH/CH2CI2) provided 210 mg (52% for 2 steps)
of 5-morpholin-4-yl-1H-pyrrolo[2,3-c]pyridine as a yellow solid. TLC (silica, 5%
MeOH/CH2CI2): Rf = 0.40. MS (electrospray): exact mass calculated for
C11H13N3O, 203.11; m/z found, 204.2 [M+H]+.
C. 4-(5-Morpholin-4-yl-1H-pyrrolo[2,3-c]pyridin-3-yl)-piperidine-1-carboxylic
acid tert-butyl ester.
A solution of 200 mg (1.0 mmol) of 5-morpholin-4-yl-1H-pyrrolo[2,3-c]pyridine
and 398 mg (2.0 mmol, 2 eq) of 4-oxo-piperidine-1-carboxylic acid tert-butyl
ester in 5 mL of MeOH was treated with 224 mg (4.0 mmol, 4 eq) of potassium
hydroxide. The reaction mixture was stirred at 65 °C for 12 h and volatiles were
removed. The crude product was partitioned between CH2Cl2 (100 mL) and 20
mL of H2O. The organic layer was washed with H2O (2 x 20 mL), dried over
Na2SO4 and concentrated. The yellow powder was treated with 630 mg (10
mmol, 10 eq) of ammonium formate and 10% Pd-C (50 mg). The reaction
mixture was stirred at 65 °C for 1 h. The reaction mixture was then filtered
through a pad of celite and concentrated to obtain a yellow solid. Column
chromatography (silica, 5% MeOH/CH2CI2) provided 180 mg (47% for 2 steps)
of a yellow solid. TLC (silica, 5% MeOH/CH2Cl2): Rf= 0.40. MS (electrospray):
exact mass calculated for C21H30N4O3, 386.23; m/z found, 387.2 [M+H]+.

P. 1-[5-Methanesulfonyl-3-(4-trifluoromethyl-phenyl)-4,5,6,7-
tetrahydropyrazolo[4,3-c]pyridin-1-yl]-3-[4-(5-rnorpholin-4-yl-1 H-pyrrolo[2,3-
c]pyridin-3-yl)-piperidin-1-yl]-propah-2-ol.
4-(5-Morpholin-4-yl-1H-pyrrolo[2,3-c]pyridin-3-yl)-piperidine-1-cart)oxylic acid
tert-butyl ester (180 mg, 0.47 mmol) was dissolved in 3.0 mL of CH2CI2 and
treated with 2.5 mL of trifluoroacetic acid. The reaction mixture was stirred at
25 °C for 1h before all voiatiles were removed. The solid was dissolved in
MeOH (20 mL) and neutralized with DOWEX 550A OH anton exchange resin
to pH 8. The resin was then filtered off and MeOH was removed under
reduced pressure. The residue was dissolved in 2.5 mL of PrOH and treated
with 187 mg (0.47 mmol, 1 eq) of 5-methanesutfonyl-1-oxiranylmethyl-3-(4-
trifluoromethyl-phenyl)-4,5,6,7-tetrahydro-1H-pyrazdo[4;3-c]pyridine. The
reaction was stirred at 85 °C for 3 h before solvent was removed. Column
chromatography (silica, 5-10% MeOH/CH2CI2 then 5-10% (2 N NH3 in
MeOH)/CH2CI2) provided 97 mg (30%) of the title compound. TLC (silica, 5%
MeOH/CH2CI2): Rf = 0.25. MS (electrospray): exact mass calculated for
C33H40F3N7O4S, 687.28; m/z found, 688.3 [M+H]+. 1H NMR (400 MHz, CDCI3):
8.47 (br s, 1H), 8.44 (d, J - 1.0 Hz, 1H), 7.70 and 7.65 (AB pattern, J = 8.4 Hz.
4H), 7.03 (d, J = 2.1 Hz, 1H), 6.76 (s, 1H), 4.58- 4.50 (m. 2H), 4.21-4.00 (m,
3H), 3.90 (t, J = 4.5 Hz, 4H), 3.72-3.58 (m, 2H), 3.40 (t, J = 4.5 Hz, 4H), 3.10-
2.85 (m, 4H), 2.88 (s, 3H), 2.80-2.70 (m, 1H), 2.52-2.41 (m, 3H), 2.20-2.00 (m,
3H), 1.80-1.60 (m,2H).


1 -[4-(6-Dimethylamino-1H-pyrrolo[3,2-c]pyridin-3-yl)-piperidin-1-yl]-3-[5-
methanesulfonyl-3-(4-trifluoromethyl-phenyl)-4,5,6,7-tetrahydro-pyrazolo[4,3-
c]pyridin-1-yl]-propan-2-ol.
A. Dimethyl-(5-methyl-4-nitro-1-oxy-pyridin-2-yl)-amine.
A solution of 2-bromo-5-methyl-4-nitro-pyricline 1-oxide (674 mg, 2.78 mmol) in
2 M dimethylamine in methanol (20 mL) was heated at 65 °C for 16 h. The
solvent was evaporated under reduced pressure. The residue was purified by
column chromatography (silica, 30-80% EtOAc/hexanes) to obtain 290 mg
(53%) of the desired product. TLC (silica, 50% EtOAc/hexanes): Rf = 0.10. MS
(electrospray): exact mass calculated for C8H11N3O3, 197.08; m/z found, 198.1
[M++H]. 1H NMR (CDCI3, 400 MHz): 8.04 (s, 1H), 7.50 (s, 1H), 3.00 (s, 6H),
2.44 (s, 3H).
B. Dimethyl-(1H-pyrrolo[3,2-c]pyridin-6-yl)-amine.
A solution of dimethyl-(5-methyl-4-nitro-1-oxy-pyridin-2-yl)-amine (290 mg. 1.47
mmol) in DMF (3 mL) was treated with DMF-dimethylacetal (390 ?L, 2.94
mmol) and the reaction mixture was stirred at 100 °C for 4 h. All volatiles were
removed under reduced pressure. The red powder was treated with
ammonium formate (927 mg, 14.7 mmol) and 10% Pd-C (156 mg). The
reaction mixture was stirred at 65 °C for 30 min. The reaction mixture was then
filtered through a pad of celtte and concentrated to obtain a yellow solid.
Column chromatography (silica, 5% MeOH/CH2CI2) provided 100 mg (42% for
two steps) of product as a yellow solid. TLC (silica, 10% MeOH/CH2CI2): Rf =
0.2. MS (electrospray): exact mass calculated for C9H11N3, 161.10; m/z found,

162.1 (M++H]. 1H NMR (CDCl3, 400 MHz): 8.55 (8,1H), 8.28 (br s. 1H), 6.96
(dd, J = 1.96 Hz, 1.37 Hz, 1H), 6.45-6.43 (m, 1H), 6.39 (s. 1H), 3.08 (s, 6H).
C. 4-(6-Dimethylamino-1H-pyrrolo[3.2-c]pyridin-3-yl)-3.6-dihydro-2H-pyridine-
1-carboxylic acid tert-butyl ester.
Dimethyl-(1H-pyrrolo[3,2-c]pyridin-6-yl)-amine (100 mg, 0.62 mmol), 4-oxo-
piperidine-1-carboxylic acid tert-butyl ester (248 mg, 1.24 mmol) and potassium
hydroxide (139 mg, 2.48 mmol) were added in MeOH (5 mL) and heated to
reflux for 16 h. The reaction mixture was then cooled to room temperature and
poured into ice water (20 mL). The mixture was extracted with 10%
MeOH/CH2CI2 (5 x 10 mL). The organic extracts was dried over Na2SO4 and
concentrated. The residue was purified by column chromatography (silica, 0-
5% MeOH/CH2CI2) to obtain 180 mg (85%) of the title compound TLC (silica,
10% MeOH/CH2Cl2): Rf = 0.58. MS (electrospray): exact mass calculated for
C19H26N4O2, 342.21; m/z found, 343.2 (M++H). 1H NMR (CDCl3, 400 MHz): 9.09
(br s, 1H), 8.76 (s, 1H), 6.90 (d, J = 2.15 Hz, 1H), 6.32 (s, 1H), 6.10 (br s, 1H),
4.10-4.05 (m, 2H), 3.62 (t, J = 5.87 Hz, 2H), 3.03 (s, 6H), 2.52-2.44 (m, 2H),
1.46 (s, 9H).
D. 4-(6-Dimethytamino-1H-pyrrolo[3,2-c]pyridin-3-yl)-piperidine-1-carboxylic
acid tert-butyl ester.
A solution of 4-(6-dimethylamino-1H-pyrrolo[3,2-c]pyridin-3-yl)-3,6-dihydro-2H-
pyridine-1-carboxylic acid tert-butyl ester (180 mg, 0.53 mmol) in MeOH (10
mL) was treated with ammonium formate (332 mg, 5.3 mmol) and 10% Pd-C
(56 mg). The reaction mixture was stirred at 65 °C for 1 h. The reaction
mixture was then filtered through a pad of celite and concentrated to obtain an
off white solid. Column chromatography (silica, 0-5% MeOH/CH2CI2) provided
135 mg (75%) of product as a white solid. TLC (silica, 10% MeOH/CH2CI2): Rf
= 0.50. MS (electrospray): exact mass calculated for C19HaN4O2, 344.22; m/z
found, 345.2 [M++H]. 1H NMR (CDCI3, 400 MHz): 8.53 (s, 1H), 8.30 (br s, 1H),
6.67 (dd, J = 1.17 Hz, 0.78 Hz, 1H), 6.34 (d, J = 0.78 Hz, 1H), 4.33-4.16 (m,
2H), 3.05 (s, 6H), 2.97-2.80 (m, 3H), 1.99 (d, J - 12.72 Hz, 2H), 1.69-1.53 (m,
2H), 1.46 (s, 9H).

E. Dimethyl-(3-piperidin-4-yl-1H-pyrrolo[3,2-c]pyridin-6-yl)-amine.
The 4-(6-dimethylamino-1H-pyrrolo[3,2-c]pyridin-3-yl)-pipericline-1-carboxylic
acid tert-butyl ester (135 mg, 0.39 mmol) was set stirring in 1:1 TFA/CH2Cl2.
After 45 min the mixture was evaporated. The residue was dissolved in MeOH
(10 mL) and neutralized with DOWEX 550A OH anlon exchange resin to pH 8.
The resin was then filtered off and MeOH was removed under reduced .
pressure to give 96 mg (100%) of a yellow solid. MS (electrospray): exact
mass calculated for C14H20N4, 244.17; m/z found, 245.2 [M++H]. 1H NMR
(CDCI3, 400 MHz): 9.23 (br s, 1H), 8.54 (s, 1H), 6.67 (s, 1H), 6.31 (d, J = 0.98
Hz, 1H), 3.15 (d, J= 2.13 Hz, 2H), 3.02 (s, 6H), 2.91-2.81 (m, 1H), 2.81-2.72
(m, 2H), 2.01 (d, J= 12.52 Hz, 2H), 1.69-1.52 (m, 2H).
F. 1-[4-(6-Dimethylamino-1H-pyrrolo[3,2-c]pyridin-3-yl)-piperidin-1-yl]-3-[5-
rnethanesulfonyl-3-(4-trifluoromethyl-prienyl)-4,5,6,7-tetrahydro-pyrazolo[4,3-
c]pyridin-1-yl]-propan-2-ol.
Dimethyl-(3-piperidin-4-yl-1H-pyrrolo[3,2-c]pyridin-6-yl)-amine (96 mg, 0.53
mmol) and 5-methanesulfonyl-1-oxiranylmethyl-3-(4-trifluoromethyl-phenyl)-
4,5,6,7-tetrahydro-1H-pyrazolo[4,3-c]pyridine (319 mg, 0.80 mmol) were set
stirring in PrOH (10 mL) at 80 °C. After 16 h the mixture was cooled and
concentrated. The residue was purified by column chromatography (silica, 0-
10% (2 N NH3 in MeOH)/CH2CI2 to obtain 61 mg (18%) of a white solid. TLC
(silica, 10% MeOH/CH2CI2): Rf =0.12. MS (electrospray): exact mass
calculated for C31H38F7N7O3S, 645.27; m/z found, 646.3 [M++H]. 1H NMR
(CDCI3, 400 MHz): 8.53 (s, 1H), 7.93 (br s, 1H), 7.71 (d, J = 8.22 Hz, 2H), 7.64
(d, J = 8.22, 2H), 6.67 (br s, 1H), 6.33 (d, J = 0.98 Hz, 1H), 4.54 (dd, J = 14.28
Hz, 9.59 Hz, 2H), 4.22-4.10 (m, 2H), 4.04-3.97 (m, 1H), 3.74-3.57 (m, 2H),
3.13-3.06 (m, 1H). 3.05 (s, 6H), 3.03-2.87 (m, 3H), 2.85 (s, 3H), 2.82-2.71 (m,
1H), 2.50-2.37 (m, 3H), 2.20-2.11 (m, 1H), 2.06-1.97 (m, 2H), 1.82-1.61 (m,
2H).


1-[5-Methanesulfonyl-3-(4-trifluoromethyl-phenyl)-4,5,6,7-tetrahydro-
pyrazolo[4,3-c]pyridin-1-yl]-3-[4-(6-morpholin-4-yl-1H-pyrrolo[3,2-c]pyridin-3-yl)-
piperidin-1-yl]-propan-2-ol.
A. 4-(5-Methyl-4-nitro-1-oxy-pyridin-2-yl)-morpholine.
A solution of 2-bromo-5-methyl-4-nitro-pyricline 1-oxide (500 mg, 2.14 mmol) in
morpholine (15 mL) was heated at 70 °C for 16 h. The solvent was evaporated
under reduced pressure. The residue was purified by column chromatography
(silica, 30-80% EtOAc/hexanes) to obtain 480 mg (94%) of the desired product.
TLC (silica, 50% EtOAc/hexanes): Rf = 0.10. MS (electrospray): exact mass
calculated for C10H13N3O4,239.09; m/z found, 240.1 [M++H]. 1H NMR (CDCI3,
400 MHz): 8.09 (s, 1H), 7.55 (s, 1H), 3.90 (t J = 4.50 Hz, 4H), 3.36 (t, J = 4.70
Hz, 4H), 2.50 (s, 3H).
B. 6-Morpholin-4-yl-1H-pyrrolo[3,2-c]pyridine.
A solution of 4-(5-methyl-4-nitro-1-oxy-pyridin-2-yl)-morpholine (480 mg, 2
mmol) in DMF (5 mL) was treated with DMF-dimethylacetal (533 ?L, 4 mmol)
and the reaction mixture was stirred at 100 °C for 4 h. All volatiles were
removed under reduced pressure. The red powder was treated with
ammonium formate (1.26 g, 20 mmol) and 10% Pd-C (212 mg). The reaction
mixture was stirred at 65 °C for 30 min. The reaction mixture was then filtered
through a pad of celite and concentrated to obtain a yellow solid. Column
chromatography (silica, 5% MeOH/CH2CI2) provided 197 mg (49% for two
steps) of a yellow solid. TLC (silica, 10% MeOH/CH2CI2): Rf = 0.55. MS

(electrospray): exact mass calculated for C11H13N3O, 203.11; m/z found, 204.1
[M+Hf. 1H NMR (CDCI3, 400 MHz) 8.68 (br s, 1H), 8.59 (s, 1H), 7.04 (dd, J =
2.15 Hz, 1.17HZ, 1H),6.51 (s. 1H), 6.49-6.47 (m, 1H), 3.86 (t, J = 4.70 Hz.
4H), 3.40 (t, J - 4.70 Hz, 4H).
C. 4-(6-Morpholin-4-yl-1H-pyrrolo[3,2-c]pyridin-3-yl)-3,6-dihydro-2H-pyridine-1-
carboxytic acid tert-butyl ester.
6-Morpholin-4-yl-1H-pyrrolo[3,2-c]pyridine (197 mg, 0.97 mmol), 4-oxo-
piperidine-1-carboxylic acid tert-butyl ester (387 mg, 1.94 mmol) and potassium
hydroxide (218 mg, 3.88 mmol) were added in MeOH (10 mL) and heated to
reflux for 16 h. The reaction mixture was then cooled to room temperature and
poured into ice water (50 mL). The mixture was extracted with 10%
MeOH/CH2CI2 (5 x 20 mL). The organic extracts was dried over Na2SO4 and
concentrated. The residue was purified by column chromatography (silica, 0-
5% MeOH/CH2CI2) to obtain 337 mg (91%) of the desired product. TLC (silica,
5% MeOH/CH2CI2): Rf= 0.50. MS (electrospray): exact mass calculated for
C21H28N4O3, 384.22; m/z found, 749.3 [M++H]. 1H NMR (CDCI3, 400 MHz): 9.24
(br s, 1H), 8.77 (s, 1H), 6.95 (d, J = 2.15 Hz, 1H), 6.45 (s, 1H), 6.09 (br s, 1H),
4.09-4.04 (m, 2H), 3.66 (t, J = 6.06 Hz, 4H). 3.60 (t, J = 5.28 Hz, 2H), 3.25 (t, J
= 5.09 Hz, 4H), 2.38 (d, J = 6.26 Hz, 2H), 1.44 (s, 9H).
D. 4-(6-Morpholin-4-yl-1H-pyrrolo[3,2-c]pyridin-3-yl)-piperidine-1-carboxylic
acid tert-butyl ester.
4-(6-Morpholin-4-yl-1H-pyrrolo[3,2-c]pyridin-3-yl)-3,6-dihydro-2H-pyridine-1-
carboxylic acid tert-butyl ester (337 mg, 0.9 mmol) in MeOH (20 mL) was
treated with ammonium formate (568 mg, 9.0 mmol) and 10% Pd-C (95 mg).
The reaction mixture was stirred at 65 °C for 1 h. The reaction mixture was
then filtered through a pad of celite and concentrated to obtain an off-white
solid. Column chromatography (silica, 0-5% MeOH/CH2CI2) provided 340 mg
(98%) of a white solid. TLC (silica, 5% MeOH/CH2CI2): Rf = 0.40. MS
(electrospray): exact mass calculated for C21H30N4O3, 386.23; m/z found, 387.3
[M++H]. 1H NMR (CDCI3, 400 MHz) 9.14 (br s, 1H), 8.55 (s, 1H), 6.74 (d, J =
i ,96 Hz, 1H), 6.45 (s, 1H), 4.27-4.08 (m, 2H), 3.80 (t, J = 4.50 Hz. 4H), 3.34 (t

J = 4.89 Hz. 4H). 2.96-2.77 (m, 3H), 1.97 (d, J = 12.91 Hz, 2H), 1.67-1.52 (m,
2H). 1.44 (s, 9H).
E. 6-Moroholin-4-yl-3-piperidin-4-yl-1H-pyrrolo[3,2-c]pyridine.
4-(6-Morpholin-4-yl-1H-pyrrok)[3,2-c]pyriclin-3-yl)-piperidine-1-carboxyllc acid
tert-butyl ester (380 mg, 0.98 mmol) was set stirring in 1:1 TFA/CH2CI2. After
45 min the mixture was evaporated. The residue was dissolved in MeOH (20
mL) and neutralized with DOWEX 550A OH anion exchange resin to pH 8.
The resin was then filtered off and MeOH was removed under reduced
pressure to give 281 mg (100%) of a yellow solid. MS (electrospray): exact
mass calculated for C16H22N4O, 286.18; m/z found, 287.1 [M++H].
F. 1-[5-Methanesulfonyl-3-(4-trifluoromethyl-phenyl-4,5,6,7-tetrahydro-
pyrazolo[4,3-c]pyridin-1-vl]-3-[4-(6-morpholin-4-yl-1H-pyrrolo[3,2-c]pyridjn-3-yl)-
piperidin-1-yl]-propan-2-ol.
6-Morpholin-4-yl-3-piperidin-4-yl-1H-pyrrolo[3,2-c]pyridine (281 mg, 0.98 mmol)
and 5-methanesulfonyl-1-oxiranylmethyl-3-(4-trifluoromethyl-phenyl)-4,5,6,7-
tetrahydro-1H-pyrazolo[4,3-c]pyridine (591 mg, 1.47 mmol) were set stirring in
iPrOH (10 mL) at 80 °C. After 16 h the mixture was cooled and concentrated.
The residue was purified by column chromatography (silica, 0-10% (2 N NH3 in
MeOH)/CH2CI2) to obtain 468 mg (69%) of a white solid. TLC (silica, 10% (2 N
NH3 in MeOH)/CH2CI2): Rf = 0.62. MS (electrospray): exact mass calculated for
C33H40F3N7O4S, 687.28; m/z found, 688.3 [M++H]. 1H NMR (CDCI3, 400 MHz):
8.56 (s, 1H), 8.40 (br s, 1H), 7.69 (d, J = 8.41 Hz, 2H), 7.63 (d, J = 8.41, 2H),
6.73 (br s, 1H), 6.46 (s, 1H), 4.51 (dd, J = 14.28 Hz, 8.80 Hz, 2H), 4.21-4.10
(m, 2H), 4.03-3.95 (m, 1H), 3.82 (t, J = 4.11 Hz, 4H), 3.71-3.54 (m, 2H), 3.36 (t,
J = 4.89 Hz, 4H), 3.10-2.97 (m, 2H), 2.93-2.86 (m, 2H), 2.84 (s, 3H), 2.82-2.72
(m, 1H), 2.50-2.37 (m, 3H), 2.20-2.10 (m, 1H), 2.04-1.95 (m, 2H). 1.80-1.60 (m,
2H).


1-[5-Methanesulfonyl-3-(4-trifluoromethyl-phenyl)-4,5,6,7-tetrahydro-
pyrazolo[4,3-c]pyridin-1-yl]-3-[4-(6-morpholin-4-yl-5-oxy-1 H-pyrrolo[3,2-
c]pyridin-3-yl)-piperidin-1-yl]-propan-2-ol.
A. 6-Morpholin-4-yl-1H-pymoto[3,2-c]pyridine 5-oxide.
A solution of 4-(5-methyl-4-nitro-1-oxy-pyridin-2-yl)-morpholine (480 mg, 2
mmol) in DMF (5 mL) was treated with DMF-dimethylacetal (533 ?L, 4 mmol)
and the reaction mixture was stirred at 100 °C for 4 h. All volatiles were
removed under reduced pressure. The red powder was treated with
ammonium formate (1.26 g, 20 mmol) and 10% Pd-C (212 mg). The reaction
mixture was stirred at 65 °C for 30 min. The reaction mixture was then filtered
through a pad of celite and concentrated to obtain a yellow solid. Column
chromatography (silica, 5% MeOH/CH2CI2) provided 130 mg (30% for two
steps) of a yellow solid. TLC (silica, 10% MeOH/CH2CI2): Rf = 0.28. MS
(electrospray): exact mass calculated for C11H13N3O2, 219.10; m/z found, 220.1
[M+H]+. 1H NMR (CDCI3, 400 MHz): 8.42 (br s, 1H), 7.25 (s, 1H), 7.14 (s, 1H),
6.82 (s, 1H), 6.35 (s, 1H), 3.79 (t, J = 4.70 Hz, 4H), 3.18 (t, J = 4.70 Hz, 4H).
B. 4-(6-Morpholin-4-yl-5-oxy-1H-pyrrolo[3,2-c]pyridin-3-yl)-3,6-dihydro-2H-
pyridine-1-carboxylic acid tert-butyl ester.
6-Morpholin-4-yl-1H-pyrrolo[3,2-c]pyridine 5-oxide (130 mg, 0.59 mmol), 4-oxo-
piperidine-1-carboxylic acid tert-butyl ester (237 mg, 1.19 mmol) and potassium
hydroxide (133 mg, 2.37 mmol) were added in MeOH (8 mL) and heated to
reflux for 16 h. The reaction mixture was then cooled to room temperature and

poured into toe water (30 mL). The mixture was extracted with 10%
MeOH/CH2Cl2 (5 x 10 mL). The organic extracts was dried over Na2SO4 and
concentrated. The residue was purified by column chromatography (silica, 0-
5% MeOH/CH2Cl2 to obtain 140 mg (59%) of the desired product. TLC (silica.
10% MeOH/CH2CI2): Rf= 0.55. MS (electrospray): exact mass calculated for
C21H26N4O4, 400.21; m/z found, 401.2 (M++H).
C. 4-(6-Morpholin-4-yl-5-oxy-1H-pyrrolo[3,2-c]pyridin-3-yl)piperidine-1-
carboxylic acid tert-butyl ester.
4-(6-Morpholin-4-yl-5-oxy-1H-pyrrolo[3,2-c]pyridin-3-yl)-3,6-dihydro-2H-
pyridine-1-carboxylic acid tert-butyl ester (140 mg, 0.35 mmol) in EtOH (20 mL)
containing PtO2 (50 mg) was placed on a Parr hydrogenator at 60 psi H2. After
18 h mixture was filtered through celite and evaporated to give a white solid.
Column chromatography (silica, 0-5% (2 N NH3 in MeOH)/CH2CI2) provided 56
mg (40%) of a white solid. TLC (silica, 5% MeOH/CH2CI2): Rf = 0.13. MS
(electrospray): exact mass calculated for C21H30N4O4, 402.23; m/z found, 403.2
(M++H). 1H NMR (CDCI3, 400 MHz): 11.63 (br s, 1H), 8.58 (s, 1H), 6.97 (br s,
1H), 6.69 (s, 1H), 4.26-4.08 (m, 2H), 3.73 (t, J = 4.30 Hz, 4H), 3.17 (t, J = 4.50
Hz, 4H), 2.92-2.74 (m, 3H), 1.91 (d, J = 11.93 Hz, 2H), 1.62-1.50 (m, 2H), 1.43
(s, 9H).
D. 6-Morpholin-4-yl-3-piperidin-4-yl-1H-pyrrolo[3,2-c]pyridine 5-oxide.
4-(6-Morpholin-4-yl-5-oxy-1H-pyrrolo[3,2-c]pyridin-3-yl)-piperidine-1-carboxylic
acid tert-butyl ester (56 mg, 0.14 mmol) was set stirring in 1:1 TFA/CH2CI2.
After 45 min the mixture was evaporated. The residue was dissolved in MeOH
(10 mL) and neutralized with DOWEX 550A OH anion exchange resin to pH 8.
The resin was then filtered off and MeOH was removed under reduced
pressure to give 42 mg (100%) of a yellow solid. MS (electrospray): exact
mass calculated for C16H22N4O2, 302.17; m/z found, 303.1 [M++H].
E. 1-[5-Methanesulfonyl-3-(4-trifluoromethyl-phenyl)-4,5,6,7-tetrahydro-
pyrazoto[4,3-c]pyridin-1-yl]-3-[4-(6-morpholin-4-yl-5-oxy-1H-pyrrolo[3,2-
c]pyridin-3-yl) -piperidin-1-yl]-propan-2-ol.

6-Morpholin-4-yl-3-piperidin-4-yl-1H-pyrrolo(3,2-c]pyridine 5-oxide (42 mg, 0.14
mmol) and 5-methanesulfonyl-1-oxiranyfmethyt-3-(4-trifluoromethyl-phenyl)-
4,5,6,7-tetrahydro-1H-pyrazolo[4,3-c]pyridine (84 mg, 0.21 mmol) were set
stirring in 1PrOH (5 mL) at 80 °C. After 6 h the mixture was cooled and
concentrated. The residue was purified by column chromatography (silica, 0-
10% (2 N NH3 in MeOH)/CH2Cl2 to obtain 5.1 mg (5%) of a white solid. TLC
(silica, 10% (2 N NH3 in MeOH)/CH2CI2): Rf = 0.54. MS (electrospray): exact
mass calculated for C33H40F3N7O5S, 703.28; m/z found, 704.3 [M++H]. 1H NMR
(CDCI3, 400 MHz): 8.60 (s, 1H), 7.71 (d, J = 8.41 Hz, 2H), 7.66 (d, J = 8.41,
2H), 7.27 (s, 1H), 6.95 (s, 1H), 6.70 (s, 1H), 4.55 (dd, J = 14.48 Hz, 3.13 Hz,
2H), 4.23-4.11 (m, 2H), 4.05-3.97 (m, 1H), 3.84 (t, J = 4.30 Hz, 4H), 3.72-3.60
(m, 2H), 3.23 (t, J = 4.30 Hz, 4H), 3.12-2.98 (m, 2H), 2.97-2.89 (m, 2H), 2.88
(s, 3H), 2.73-2.63 (m, 1H), 2.51-2.36 (m, 3H), 2.17-2.08 (m, 1H), 1.99-1.90 (m,
2H), 1.78-1.58 (m, 2H).

6-Fluoro-3-(1-{3-[5-methanesulfonyl-3-(4-trifluoromethyl-phenyl)-4,5,6,7-
tetrahydropyrazolo[4,3-c]pyridin-1-yr|-propyl}-piperidin-4-yl)benzo[b]thiophene-
2-carboxylic acid (2-hydroxy-ethyl)-amide.
A. 1-[4-(2,4-Difluoro-benzovl)-piperidin-1-yl]-ethanone.
A stirred solution of 10 g (58.5 mmol) of 1-acetylpiperidine-4-carboxylic acid in
anhydrous dichloroethane (35 mL) was treated with 5.1 mL (70.2 mmol) of
thionyl chloride in 7 mL of dichloroethane and then heated to 60 °C for 30 min.
Another flask containing a suspension of 8.02 mL (81.8 mmol) of 1,3-
difluorobenzene and 17.9 g (134 mmol) of aluminum chloride in 55 mL of
dichloroethane was prepared, to this was added the previously prepared acid

chloride suspension in portions. The resulting suspension was refluxed for 4 h,
cooled and then poured over ice and HCI. The acidic solution was extracted
with CH2CI2 (3 x 300 mL) and the combined organic extracts were washed with
brine, dried over Na2SO4, and concentrated. The crude product was
recrystaJlized from hexanes to afford 9.5 g (61 %) of the desired product as a
white solid. MS (electrospray): exact mass calculated for C14H16F2NO2, 267.11;
m/z found, 268.1 [M+H]+, 1H NMR (CDCI3, 400 MHz): 7.87 (dt, J = 8.41, 6.65
Hz 1H), 6.98 (m, 1H). 6.88 (ddd, J = 10.96, 8.61, 2.35 Hz, 1H), 4.55 (m, 1H),
3.87 (m, 1H), 3.32 (dtt, J = 10.76. 3.91, 1.37 Hz, 1H), 3.19 (ddd, J = 13.89,
11.93, 2.93 Hz, 1H). 2.79 (ddd, J = 13.89, 12.24, 2.93 Hz, 1H), 2.10 (s, 3H),
1.95 (br d, J = 12.91 Hz, 2H), 1.72 (br m, 1H), 1.56 (br m, 1H).
B. 3-(1-Acetyl-piperidin-4-yl)-6-fluoro-benzo[b]thiophene-2-carboxylic acid
methyl ester.
To a stirred solution of 33.6 g (0.126 mol) of 1-[4-(2,4-difluoro-benzoyl)-
piperidin-1-yl]-ethanone and 13 mL (145 mol) of methyl thioglycolate in 320 mL
dry THF was added 5.8 g (145 mol) of 60% sodium hydride in mineral oil in
portions. The reaction mixture was heated to reflux overnight, allowed to cool
to room temperature and the solvent removed under reduced pressure. The
residue was then partitioned between 300 mL of CH2CI2 and 200 mL of water.
The aqueous layer was further extracted with CH2CI2 (2 x 500 mL). The
combined organic layers were washed with brine, dried over Na2SO4, and
concentrated to give a residue which was then triturated with hexanes/EtOAc
to give 27.5 g (65%) of the desired product as a white solid. MS (electrospray):
exact mass calculated for C17H18FNO3S, 335.1; m/z found, 336.1 [M+H]+. 1H
NMR (DMSO-d6. 400 MHz, a mixture of amide rotamers): 7.12 (m, 2H), 6.92
(dt, J = 8.41,1.77 Hz, 1H), 4.43 (d, J = 3.79 Hz, 1H), 4.43-4.36 (m, 1H), 3.82
(bt, J = 14.65 Hz, 1H), 3.57 (s, 3H), 2.92-2.79 (m, 1H), 2.38-2.34 (m, 1H), 1.94
(s, 1.5H), 1.93 (s, 1.5H), 1.86-1.72 (m, 1H), 1.47-1.38 (m, 1H), 1.38-1.27 (m,
0.5H), 1.27-1.16 (m, 1H), 1.15-1.03 (m, 0.5H).
C. 6-Fluoro-3-piperidin-4-yl-benzo[b]thiophene-2-carboxylic acid methyl ester
hvdrochloride salt.

A solution of 24.4 g (66.8 mmol) of 3-(1-acetyl-plperidin-4-yl)-6-fluoro-
benzo[b]thiophene-2-carboxylic acid methyl ester in 400 mL of MeOH and 50
mL of concentrated HCI was heated a reflux for 2 days. When the solution was
allowed to cod to room temperature the white precipitate was filtered, washed
with methanol and dried to give 17.9 g (74%) of product as a white powder.
MS (electrospray): exact mass calculated for C15H16FNO2S, 293.09; m/z found,
294.1 [M+H]+. 1H NMR (DMSO-d6, 400 MHz): 9.38 (br s, 1H). 9.02 (br s. 1H),
8.60 (dd, J = 9.19, 5.09 Hz, 1H), 7.98 (dd, J = 9.00, 2.54 Hz, 1H), 7.36 (dt, J =
9.00, 2.54 Hz, 1H), 4.37 (br t, J - 12.72 Hz, 1H), 3.87 (s, 3H), 3.40 (br d, J =
11.93 Hz, 2H), 3.02 (q, J = 11.35 Hz, 2H), 2.61 (dq, J = 13.30, 3.72 Hz, 2H),
1.77 (brd, J = 12.91 Hz, 2H).
D. 3-[5-Methanesulfonyl-3-(4-trifluoromethyl-phenyl)-4,5,6,7-tetrahydro-
pyrazolo[4,3-c]pyridin-1-yl]-propan-1-ol.
Cs2CO3 (33.74 g, 103.5 mmol) was added to a solution of 5-methanesulfonyl-3-
(4-rifluoromethyl-phenyl)-4,5,6,7-tetrahydro-1H-pyrazolo[4,3-c]pyridine (29.8 g,
86.3 mmol) in anhydrous DMF (70 mL) and stirred for 25 min. 3-Bromo-1-
propanol (8.6 mL, 13.2 g, 94.9 mmol) was added and stirred under N2 at room
temperature for 18 h. Water (500 mL) was added to the reaction and stirred for
5 min. The precipitated material was filtered out and washed with water (4 X
100 mL) and dried. The crude material (31.0 g) was taken up in anhydrous
DMF (65 mL) and Cs2CO3 (33.74 g, 103.5 mmol) was added, and stirred for 10
min. Then 3-bromo-1-propanol (8.6 mL, 13.2 g, 94.9 mmol) and MeOH (6.0
mL, 4.75 g, 148 mmol) were added and stirring continued under N2 at rt for 15
h. Water (500 mL) was added to the reaction and stirred for 10 min. The
precipitated material was filtered and washed with water (3 X 100 mL). The
filter cake was dissolved in CH2CI2 (200 mL) and washed with brine (50 mL),
dried (Na2SO4), and concentrated. The solid was triturated with Et2O (200 mL),
filtered, then washed with Et2O, and dried to furnish 16.0 g of the desired
compound. The mother liquor was chromatographed (silica, 0-10%
acetone/EtOAc) to obtain an additional 3.0 g of the title compound. The
combined yield was 54.6%. MS (electrospray): exact mass calculated for
C17H20F3N3O3S, 403.12; m/z found, 404.0 [M+H]+. 1H NMR (400 MHz, CDCI3):

7.71 (d, J = 8.2 Hz, 2H), 7.66 (d, J = 8.5 Hz, 2H), 4.55 (s, 2H), 4.23 (t J = 6.5
Hz, 2H), 3.70-3.63 (m, 4H), 2.90 (s. 3H). 2.90 (t J = 5.1 Hz. 2H), 2.62 (t J =
5.9 Hz, 1H), 2.06 (q, J = 6.1 Hz, 2H).
E. 3-[5-Methanesulfonyl]-3-(4-trifluoromethyl-phenyl)-4,5,6,7-tetrahydro-
pyrazolo[4,3-c]pyridin-1-yl]-propionaldehyde.
Dess-Martin periodinane (3.45 g, 8.2 mmol) was added to a solution of 3-[5-
methanesulfonyl-3-(4-trifluoromethyl-phenyl)-4,5,6,7-tetrahydro-pyrazolo[4,3-
c]pyridin-1-yl]-propan-1-ol (3.0 g, 7.4 mmol) in CH2CI2 (20 mL) at 0 °C under N2.
After 15 min, the reaction was allowed to warm to room temperature and stirred
for another 1.5 h. The reaction was diluted with Et2O (60 mL) and 20 % aq.
NaHCO3 (35 mL) was added slowly (caution! rapid gas evolution). Then
Na2S2O3 was added and stirred at room temperature for 30 min. The layers
were separated and the aqueous portion was extracted with Et2O (2x30 mL).
The combined organic extracts were washed with brine, dried (Na2SO4) and
concentrated. MPLC (silica, 1-10% MeOH/CH2CI2) afforded 2.53 g of the
desired aldehyde in 85% yield. MS (eiectrospray): exact mass calculated for
C17H18F3N3O3S, 401.11; m/z found, 402.1 [M+H]. 1H NMR (400 MHz, CDCI3):
9.82 (s, 1H), 7.63 (d, J = 8.4 Hz, 2H), 7.58 (d, J = 8.4 Hz, 2H), 4.68 (s, 2H),
4.25 (t, J = 6.1 Hz, 2H), 3.63 (t, J = 5.8 Hz, 4H), 3.14 (t, J = 6.1 Hz, 2H), 2.92 (t,
J = 5.8 Hz, 2H),2.81(s, 3H).
F. 6-Fluoro-3-(1-{3-[5-methanesulfonyl-3-(4-trifluoromethyl-phenyl)-4,5,6,7-
tetrahydro-pyrazolo[4,3-c]pyridin-1-yl]-propyl}-piperidin-4-yl)benzo[b]thiophene-
2-carboxylic acid methyl ester.
To a stirred solution of 410 mg (1.25 mmol) of 6-fluoro-3-piperidin-4-yl-
benzo[b]thiophene-2-carboxylic acid methyl ester hydrochloride salt in 10 mL of
dichloromethane and 0.18 mL (1.25 mmol) of triethylamine was added 500 mg
of 3-[5-methanesulfonyl-3-(4-trifluoromethyl-phenyl)-4,5,6,7-tetrahydro-
pyrazolo[4,3-c]pyridin-1-yl]-propionaldehyde (1.25 mmol) and 2 g of NaHCO3.
The mixture was stirred for 4 h before the portion wise addition of 792 mg (3.73
mmol) sodium triacetoxyborohydride. The reaction was stirred at room
temperature for 3 h before quenching with 20 mL of water. The aqueous

phase was extracted with CH2CI2 (3 x 50 mL). The combined organic layers
were then washed with brine, dried over Na2SO4, and concentrated. The crude
product was purified by column chromatography (silica, 0-5% MeOH/CH2CI2) to
afford 650 mg (77%) of a white solid. MS (electrospray): exact mass
calculated for C32H34F4N4O4S2: 678.20; m/z found, 679.2 [M+H]+. 1H NMR
(CDCI3, 400 MHz): 7.74 and 7.66 (A and B of AB quartet, J = 8.22 Hz, 4H),
7.50 (dd, J = 8.41, 2.54 Hz 1H), 7.14 (t, J = 8.22 Hz, 1H), 4.56 (s, 2H), 4.17 (m,
3H), 3.91 (s, 3H), 3.70 (t, J = 5.67 Hz, 2H), 3.03 (br m, 2H), 3.00 (t, J = 5.67
Hz, 2H), 2.90 (s, 3H), 2.40 (br m, 4H), 2.13 (br m, 4H), 1.76 (br d, J = 11.15 Hz,
4H).
G. 6-Fluoro-3-(1-{3-[5-methanesulfonyl-3-(4-trifluoromethyl-phenyl)-4,5,6,7-
tetrahydro-pyrazolo[4,3-c]pyridin-1-vl]propyl}-piperidin-4-yl)benzo[b]thiophene-
2-carboxylic acid.
To a stirred solution of 635 mg (0.94 mmol) of 6-fluoro-3-(1-{3-[5-
methanesutfonyl-3-(4-trifluoromethyl-phenyl)-4,5,67-tetrahydro-pyrazolo[4,3-c
]pyridin-1-yl]-propyl}-piperidin-4-yl)-benzo[b]thiophene-2-carboxylic acid methyl
ester in 10 mL of THF was treated a solution of 53 mg (0.94 mmol) of KOH in
0.5 mL of water. This was stirred overnight, after the hydrolysis was deemed
complete 1 mL of 1 N HCl solution was added. This was then extracted with
EtOAc (3 x 30 mL). The combined organic layers were then washed with brine,
dried over Na2SO4, and concentrated to yield 622 mg (100%) of a white solid.
MS (electrospray): exact mass calculated for C31H32F4N4O4S2: 664.18; m/z
found, 665.2 [M+H]+. 1H NMR (DMSO-d6, 400 MHz): 8.12 (dd, J = 8.81, 5.28
Hz, 1H), 7.83 and 7.76 (A and B of AB quartet, J = 8.41 Hz, 4H), 7.17 (br t, J =
8.61 Hz, 1H), 4.47 (s, 2H), 4.29 (br s, 1H), 4.16 (t, J = 7.04 Hz, 2H), 3.53 (t, J =
5.67 Hz, 2H), 3.28 (br m, 4H), 3.00 (s, 3H), 2.96 (m, 2H), 2.73 (br s, 2H), 2.52
(br m, 2H), 2 .13 (br m, 2H), 1.76 (br m, 2H).
H. 6-Fluoro-3-(143-[5-methanesulfonyl-3-[4-trifluoromethyl-phenyl)-4,5,6,7-
tetrahydro-pyrazolo[4,3-c]pyridin-1-yl]-propyl}-piperidin-4-yl)benzo[b]thiophene-
2-carboxylic acid (2-hydroxy-ethyl)-amide.

A stirred solution of 20 mg (0.03 mmol) of 6-fluoro-3-(1-{3-{5-methanesulfonyl-
3-(4-trifluoromethyl-phenyl)-4,5,6,7-tetrahydro-pyrazolo[4,3-c]pyridin-1-yl]-
propyl}-piperidin-4-yl}-benzo[b]thiophene-2-carboxylic acid in 0.3 mL of dry
DMF was treated with 14 mg (0.036 mmol) of HBTU and 8 ?L (0.045 mmol) of
DIEA. The solution was stirred for 5 min before the addition of 0.01 mL (0.15
mmol) of ethanol amine. The reaction was stirred at room temperature for 30
min then partitioned between EtOAc (30 mL) and saturated NaHCO3 (20 mL).
The aqueous layer was further extracted with EtOAc (2 x 20 mL). The
combined organic layers were then washed with brine, dried over Na2SO4, and
concentrated. Purification by column chromatography (silica, 5-10% of 2 N
NH3 in MeOH/CH2CI2) yielded 16 mg (76%) of a white solid. MS (electrospray):
exact mass calculated for C33H37F4NSO4S2: 707.22; m/z found, 708.2 [M+H]+.
1H NMR(CDCI3, 400 MHz): 7.97 (br s, 1H), 7.73 and 7.66 (A and B of AB
quartet, J = 8.41 Hz, 4H), 7.49 (dd, J = 8.41, 2.35 Hz, 1H), 7.15 (dt, J = 8.61,
2.54 Hz, 1H), 6.41 (t, J = 5.67 Hz, 1H), 4.56 (s, 2H), 4.16 (t. J = 7.04 Hz, 2H).
3.84 (dd, J - 5.28, 4.70 Hz, 2H), 3.70 (t, J = 5.67 Hz, 2H), 3.62 (m, 2H), 3.58
(br s, 1H), 3.05 (br m, 2H), 2.97 (t, J = 5.67 Hz, 2H), 2.91 (s, 3H), 2.40 (br m,
4H), 2.13 (br m, 4H), 1.84 (brd, J = 12.32 Hz, 2H).

6-Fluoro-3-(1-{3-[5-methanesutonyl-3-(4-trifluoromethyl-phenyl)-4,5,6,7-
tetrahydro-pyrazolo[4,3-c]pyridin-1-yl]-propyl}-piperidin-4-yl)benzo[b]thiophene-
2-carboxylic acid (2-amino-ethyl)-amide.
A stirred solution of 300 mg (0.43 mmol) 6-fluoro-3-(1-{3-[5-methanesulfonyl-3-
(4-trifluoromethyl-phenyl)-4,5,6,7-tetrahydro-pyrazolo[4,3-c]pyridin-1-yl]-propyl}-
piperidin-4-yl)-benzo[b]thiophene-2-carboxylic acid in 5 mL of dry DMF was

treated with 812 mg (2.14 mmol) of HBTU and 0.75 mL (4.28 mmol) of DlEA.
The solution was stirred for 5 min before the addition of 0.28 mL (4.28 mmol) of
ethylenediamine. The reaction was stirred at room temperature for 30 min then
partitioned between EtOAc (30 mL) and saturated sodium bicarbonate (20 mL).
The aqueous layer was further extracted with EtOAc (2 x 20 mL). The
combined organic layers were then washed with brine, dried over Na2SO4, and
concentrated. Purification by column chromatography (silica, 5-10% of (2 N
NH3 in MeOH)/CH2CI2) afforded 200 mg (66%) of a clear oil. MS (electrospray):
exact mass calculated for C33H38F4N6O3S2: 706.24; m/z found, 707.2 [M+H]+.
1H NMR (CD3OD, 400 MHz): 8.14 (m, 1H), 7.84 and 7.72 (A and B of AB
quartet, J = 8.41 Hz, 4H), 7.68 (m, 1H), 7.21 (dt, J = 8.81, 2.74 Hz, 1H), 4.54
(s, 2H), 4.27 (t, J = 6.26 Hz, 2H), 4.00-3.90 (m, 2H), 3.76-3.61 (m, 8H), 3.28-
3.23 (br m, 1H), 3.19-3.09 (or m, 3H), 2.98 (s, 3H), 2.97-2.93 (m, 2H), 2.67 (br
m, 2H), 2.52-2.37 (m, 3H), 2.02 (br d, J = 13.89 Hz, 2H).

6-Fluoro-3-(1-{3-[5-methanesulfonyl-3-(4-trifluoromethyl-phenyl)-4,5,6,7-
tetrahydro-pyrazolo[4,3-c]pyridin-1-yl]-propyl}-piperidin-4-yl)benzo[b]thiophene-
2-carboxylic acid (2-morpholin-4-yl-ethyl)-amide.
A stirred solution of 20 mg (0.03 mmol) of 6-fluoro-3-(1-{3-[5-methanesulfonyl-
3-(4-trifluoromethyl-phenyl)-4,5,6,7-tetrahydro-pyrazolo[4,3-c]pyridin-1-yl]-
propyl}-piperidin-4-yl)-benzo[b]thiophene-2-carboxylic acid in 0.3 mL of dry
DMF was treated with 14 mg (0.036 mmol) of HBTU and 8 ?L (0.045 mmol) of

DIEA. The solution was stirred for 5 min before the addition of 20 ?L (0.15
mmol) of 4-(2-aminoethyl)morpholine. The reaction was stirred at room
temperature for 30 min then partitioned between EtOAc (30 mL) and saturated
NaHCO3 (20 mL). The aqueous layer was further extracted with EtOAc (2 x 20
mL). The combined organic layers were then washed with brine, dried over
Na2SO4, and concentrated. Purification by column chromatography (silica, 5-
10% of (2 N NH3 in MeOH)/CH2CI2) afforded 15 mg (65%) of a white solid. MS
(electrospray), exact mass calculated for C37H44F4N6O4S2: 776.28; m/z found,
777.3 [M+H]+. 1H NMR (CDCI3, 400 MHz): 8.07 (br s, 1H), 7.73 and 7.66 (A
and B of AB quartet, J = 8.41 Hz, 4H), 7.50 (dd, J = 8.41, 2.35 Hz, 1H), 7.14
(dt, J = 8.61, 2.54 Hz, 1H), 6.64 (t, J = 4.70 Hz, 1H), 4.56 (s, 2H), 4.16 (t, J =
6.85 Hz, 2H), 3.80-3.67 (m, 7H), 3.53 (q, J = 5.48 Hz, 2H), 3.03 (br m, 2H),
2.98 (t, J = 5.67 Hz, 2H), 2.90 (s, 3H), 2.60 (t, J = 5.87 Hz, 2H), 2.38 (br m,
4H), 2.12 (br m, 4H), 1.86-1.73 (br m, 3H).

1-[1-{2-Hydroxy-3-[4-(1H-indol-3-yl)-piperidin-1-yl]-propyl}-3-(4-trifluoromethyl-
phenyl)-1,4,6,7-tetrahydro-pyrazolo[4,3-c]pyridin-5-yl]-ethanone.


1-[4-(5-Fluoro-1H-indol-3-yl)-piperidin-1-yl]-3-{5-methanesulfonyl-3-(4-
trifluoromethyl-phenyl)-4,5,6,7-tetrahyclro-pyrazolo[4,3-c]pyridin-1-yl]-propan-2-
ol.

1-[3-(4-Bromo-phenyl)-5-methanesulfonyl-4,5,6,7-tetrahydro-pyrazolo[4,3-
c]pyridin-1-yl]-3-[4-(5-chloro-1H-indol-3-yl)-piperidin-1-yl]-propan-2-ol.

1-[3-(4--Bromo-phenyl)-5-methanesulfonyl-4,5,6,7-tetrahydro-pyrazolo[4,3-
c]pyridin-1-yl]-3-[4-(5-chloro-2-methyl-1H-indol-3-yl)-piperidin-1-yl]-propan-2-ol.


1-{5-Methanesulfonyl-3-(4-trifluoromethyl-phenyl)-4,5,6,7-tetrahyclro-
pyrazolo[4,3-c]pyridin-1-yl]-3-[4-(5-methyl-1H-indol-3-yl)-piperidin-1-yl]-propan-
2-ol.

3-(1-{2-Hyclroxy-3-[5-methanesulfonyl-3-(4-trifluoromethyl-phenyl)-4,5,6,7-
tetrahydro-pyrazolo[4,3-c]pyridin-1-yl]-propyl}-piperidin-4-yl)-1H-indole-5-
carbonitrile.

1-[5-Methanesulfonyl-3-(4-trifluoromethyl-phenyl)-4,5,6,7-tetrahydro-
pyrazolo[4,3-c]pyridin-1-yl]-3-[4-(5-methoxy-1H-indol-3-yl)-piperidin-1-yl]-
propan-2-ol.


3-(1-{2-Hydroxy-3-[5-methanesulfonyl-3-(4-trifluoromethyl-phenyl)-4,5,6,7-
tetrahydro-pyrazolo[4,3-c]pyridin-1-yl]-propyl}-piperidin-4-yl)-1H-indole-5-
carboxylic acid ethyl ester.

1-[4-(6-Chloro-1H-indol-3-yl)-piperidin-1-yl]-3-[5-methanesulfonyl-3-(4-
trifluoromethyl-phenyl)-4,5,6,7-tetrahydro-pyrazolo[4,3-c]pyridin-1-yl]-propan-2-
ol.


1-[1-(3-{4-[6-Chloro-1-(2-morpholin-4-yl-ethyl)-1H-indol-3-yl]-piperidin-1-yl}-2-
hydroxy-propyl)-3-(4-trifluoromethyl-phenyl)-1,4,6,7-tetrahydro-pyrazolo[4,3-
c]pyridin-5-yl]-ethanone.

1-[5-Methanesulfonyl-3-(4-trifluoromethyl-phenyl)-4,5,6,7-tetrahydro-
pyrazolo[4,3-c]pyridin-1-yl]-3-{4-(1H-pyrrolo[3,2-b]pyridin-3-yl)-piperidin-1-yl]-
propan-2-ol.

1-[5-Methanesulfonyl-3-(4-trifluoromethyl-phenyl)-4,5,6,7-tetrahydro-
pyrazolo[4,3-c]pyridin-1-yl]-3-[4-(1H-pyrrolo[2,3-c]pyridin-3-yl)-piperidin-1-yl]-
propan-2-ol.


1-[5-Methanesulfonyl-3-(4-trifluoromethyl-phenyl)-4,5,6,7-tetrahydro-
pyrazolo[4,3-c]pyridin-1-yl]-3-[4-(5-oxy-1H-pyrrolo[3,2-c]pyridin-3-yl)-piperidin-
1-yl]-propan-2-ol.

1 -[4-(5-Dimethylamino-1H-pyrrolo[3,2-b]pyridin-3-yl)-piperidin-1-yl]-3-[5-
methanesulfonyl-3-(4-trifluorpmethyl-phenyl)-4,5,6,7-tetrahydro-pyrazolo[4,3-
c]pyridin-1-yl]-propan-2-ol.


1-[4-(5-Dimethylamino-1H-pyrrolo[2,3-c]pyridin-3-yl)-piperidin-1-yl]-3-[5-
methanesulfonyl-3-(4-trifluoromethyl-phenyl)-4,5,6,7-tetrahydro-pyrazolo[4,3-
c]pyridin-1-yl]-propan-2-ol.

3-(1-{2-Hydroxy-3-[5-methanesulfonyl-3-(4-trifluoromethyl-phenyl)-4,5,6,7-
tetrahydro-pyrazolo[4,3-c]pyridin-1-yl]-propyl}-piperidin-4-y1)-1H-pyrrolo[2,3-
b]pyridine-6-carbonitrile.

1-[5-Methanesulfonyl-3-(4-trifluoromethyl-phenyl)-4,5,6,7-tetrahydro-
pyrazolo[4,3-c]pyridin-1-yl]-3-{4-[1-(2-morpholin-4-yl-ethyl)-1H-pyrrolo[2,3-
b]pyridin-3-yl]-piperidin-1-yl}-propan-2-ol.


1-[5-Methanesulfonyl-3-(4-trifluoromethyl-phenyl)-4,5,6,7-tetrahyclro-
pyrazolo[4,3-c]pyridin-1-yl]-3-{4-(7-morpholin-4-yl-1H-pyrrolo[2,3-c]pyridin-3-yl)-
piperidin-1-yl]-propan-2-ol.

1-[4-(6-Fluoro-2-hydroxymethyl-benzo[b]thiophen-3-yl)-piperidin-1-yl]-3-[5-
methanesulfonyl-3-(4-trifluoromethyl-phenyl)-4,5,6,7-tetrahydro-pyrazolo[4,3-
c]pyridin-1-yl]-propan-2-ol.


6-Fluoro-3-(1-{2-hydroxy-3-[5-methanesutfonyl-3-{4-trifluoromethyl-phenyl)-
4,5,67-tetrahydro-pyrazolo[4,3-c]pyridin-1-yl]-propyl}-piperidin-4-yl)-
benzo[b]thiophene-2-carbaldehyde.

6-Fluoro-3-(1-{2-hydroxy-3-[5-methanesulfonyl-3-(4-trifluoromethyl-phenyl)-
4,5,6,7-tetrahydro-pyrazolo[4,3-c]pyridin-1-yl]-propyl}-piperidin-4-yl)-
benzo[b]thiophene-2-carboxylic acid methyl ester.

6-Fluoro-3-(1-{3-[5-methanesulfonyl-3-(4-trifluoromethyl-phenyl)-4,5,6,7-
tetrahydro-pyrazolo[4,3-c]pyridin-1-yl-propyl}-piperidin-4-yl)benzo[b]thiophene-
2-carboxylic acid amide.


6-Fluoro-3-(1-{3-[5-methanesulfonyl-3-(4-trifluoromethyl-phenyl)-4,5,6,7-
tetrahydro-pyrazolo[4,3-c]pyridin-1-yl]-propyl}-pipericlin-4-yl)benzo[b]thiophene-
2-carboxylic acid ethylamide.
EXAMPLE 37
Cathepsin S Inhibition Assay.
Recombinant human cathepsin S (CatS) was expressed in the
baculovirus system and purified in one step with a thiopropyl-sepharose
column. 10-L yielded ~700 mg of CatS and N-terminal sequencing confirmed
identity. The assay is run in 100 mM sodium acetate pH 5.0 containing 1 mM
DTT and 100 mM NaCI. The substrate for the assay is
(Aedens)EKARVLAEAA(Dabcyl)K-amide
The Km for the substrate is around 5 uM but the presence of substrate inhibition
makes kinetic analysis difficult. With 20 uM substrate the assay rate is linear
over the range of 1-8 ng CatS in 100 ?l reaction. Using 2 ng/well of CatS, the
production of product is linear and yields ~7-fold signal after 20 min with only
20% loss of substrate. Primary assays are run by quenching the reaction after
20 min with 0.1% SDS and then measuring the fluorescence. For other
assays, measurements are taken every min for 20 min. The rate is calculated
from the slope of the increase and the percent inhibition is calculated from this
(See Tables 1, 2 and 3 below).





EXAMPLE 101
1-(3-(4-Chloro-3-methyl-phenyl)-1-{2-hydroxy-3-[4-(1H-indol-3-yl)-piperidin-1-
yl]-propyl}-1,4,6,7-tetrahydro-pyrazolo[4,3-c]pyriclin-5-yl)-ethanone
EXAMPLE 102
1-[1-{3-{4-(5-Chloro-1H-indol-3-yl)-piperidin-1-yl]-2-hydroxy-propyl}-3-(4-
trifluoromethyl-phenyl)-1,4,6,7-tetrahydro-pyrazdo[4,3-c]pyridin-5-yl]-ethanone
EXAMPLE 103
1-{3-[4-(5-Chloro-1H-indol-3-yl)-piperidin-1-yl]-propyl}-5-methanesulfonyl-3-(4-
trifluorornethyl-phenyl)-4,5,6,7-tetrahydro-1H-pyrazolo[4,3-c]pyridine
EXAMPLE 104
3-(1-{2-Hydroxy-3-[5-methanesulfonyl-3-{4-trifluoromethyl-phenyl)-4,5,6,7-
tetrahydro-pyrazolo[4,3-c]pyrldin-1-yl]-propyl}-piperidin-4-yl)-1H-indole-5-
carbonitrile
EXAMPLE 105
1-[4-(6-Chloro-1-methyl-1H-indol-3-yl)-piperidin-1-yl]-3-[5-methanesulfonyl-3-(4-
trifluoromethyl-phenyl)-4,5,6,7-tetrahydro-pyrazolo[4,3-c]pyridin-1-yl]-propan-
2-ol
EXAMPLE 106
1-[4-(6-Chloro-1-methanesulfonyl-1H-indol-3-yl)-piperidin-1-yl]-3-[5-
methanesulfonyl-3-(4-trifluoromethyl-phenyl)-4,5,6,7-tetrahydro-pyrazolo[4,3-
c]pyridin-1-yl]-propan-2-ol
EXAMPLE 107
1-[3-{4-Bromo-phenyl)-5-methanesulfonyl-4,5,6,7-tetrahydro-pyrazolo[4,3-
c]pyridin-1-yl]-3-[4-(7-chloro-1H-indol-3-yl)-piperidin-1-yl]-propan-2-ol

EXAMPLE 108
3-(1-{3-[3-(4-Bromo-phenyl)-5-methanesulfonyl-4,5,6,7-tetrahydro-pyrazolo[4,3-
c]pyridin-1-yl]-2-hydroxy-propyl}-piperidin-4-yl)-1H-indole-5-carbonitrile
EXAMPLE 109
1-[3-(4-Bromo-phenyl)-5-methanesulfonyl-4,5,6,7-tetrahydro-pyrazolo[4,3-
c]pyridin-1-yI]-3-{4-[6-chloro-1-(2-morpholin-4-yl-ethyl)-1H-indol-3-yl]-piperidin-
1-yl}-propan-2-ol
EXAMPLE 110
1-[3-(4-Bromo-phenyl)-1-(3-{4-[6-chloro-1-(2-morpholin-4-yl-ethyl)-1H-indol-3-
yl]-piperidin-1-yl}-hydroxy-propyl)-1,4,6,7-tetrahydro-pyrazolo[4,3-c]pyridin-5-
yl]-ethanone
EXAMPLE 111
1-[1-{2-Hydroxy-3-[4-(1H-pyrrolo[2,3-b]pyridin-3-yl)-piperidin-1-yl]-propyl}-3-(4-
trifluoromethyl-phenyl)-1,4,6,7-tetrahydro-pyrazolo[4,3-c]pyridin-5-yl]-ethanone
EXAMPLE 112
1-[3-(4-Bromo-phenyl)-5-methanesulfonyl-4,5,6,7-tetrahydro-pyrazolo[4,3-
c]pyridin-1-yl]-3-[4-(1H-pyrrolo[2,3-b]pyridin-3-yl)-piperidin-1-yl]-propan-2-ol
EXAMPLE 113
1 -(3-(4-Bromo-phenyl)-1-{2-hydroxy-3-[4-(1H-pyrrolo[2,3-b]pyridin-3-yl)-
piperidin-1-yl]-propyl}-1,4,6,7-tetrahydro-pyrazolo[4,3-c]pyridin-5-yl)-ethanone
EXAMPLE 114
1-[1-(2-Hydroxy-3-{4-[1-(2-morpholin-4-yl-ethyl)-1H-pyrrolo[2,3-b]pyridin-3-yl]-
piperidin-1-yl}-propyl)-3-(4-trifluoromethyl-phenyl)-1,4,6,7-tetrahydro-
pyrazolo[4,3-c]pyridin-5-yl]-ethanone

EXAMPLE 115
5-Methanesulfonyl-1-{3-[4-(1H-pyrrolo[2,3-b]pyridin-3-yl)-3,6-dihydro-2H-
pyridin-1-yl]-propyl}-3-(4-trifluoromethyl-phenyl)-4,5,6,7-tetrahydro-1H-
pyrazolo[4,3-c]pyridine
EXAMPLE 116
5-Methanesulfonyl-1-{3-[4-(1H-pyrrolo[2,3-b]pyridin-3-yl)-piperidin-1-yl}-propyl}-
3-(4-trifluoromethyl-phenyl}-4,5,6,7-tetrahydro-1H-pyrazolo[4,3-c]pyridine
EXAMPLE 117
1-[3-(4-Bromo-phenyl)-5-rnethanesulfonyl-4,5,6,7-tetrahydro-pyrazolo[4,3-
c]pyridin-1-yl]-3-{4-[1-(2-morpholin-4-yl-ethyl)-1H-pyrrolo[2,3-b]pyridin-3-yl]-
piperidin-1-yl}-propan-2-ol
EXAMPLE 118
1-[3-(4-Bromo-phenyl)-1-(2-hydroxy-3-{4-[1-(2-morpholin-4-yl-ethyl)-1H-
pyrrolo[2,3-b]pyridin-3-yl]-piperidin-1-yl}-propyl)-1,4,6,7-tetrahydro-
pyrazolo[4,3-c]pyridin-5-yl]-ethanone
EXAMPLE 119
6-Chloro-3-(1-{2-hydroxy-3-[5-methanesulfonyl-3-(4-trifluoromethyl-phenyl)-
4,5,6,7-tetrahydro-pyrazolo[4,3-c]pyridin-1-yl]-propyl}-piperidin-4-yl)-pyrrolo[2,3-
b]pyridine-1-carboxylic acid methyl ester
EXAMPLE 120
1-[4-(6-Chloro-1H-pyrrolo[2,3-b]pyridin-3-yl)-piperidin-1-yl]-3-[5-
methanesulfonyl-3-trifluoromethyl-phenyl)-4,5,6,7-tetrahydro-pyrazolo[4,3-
c]pyridin-1-yl]-propan-2-ol
EXAMPLE 121
1-[5-Methanesulfonyl-3-(4-trifluoromethyl-phenyl)-4,5,6,7-tetrahydro-
pyrazolo[4,3-c]pyridin-1-yl]-3-[4-(7-oxy-1H-pyrrolo[2,3-b]pyridin-3-yl)-piperidin-
1-yl]-propan-2-ol

EXAMPLE 122
1-[5-Methanesutfonyl-3-(4-trifluoromethyl-phenyl)-4,5,6,7-tetrahydro-
pyrazolo[4,3-c]pyridin-1-yl]-[4-(6-morpholin-4-yl-1H-pyrrolo[2,3-b]pyriclin-3-yl}-
piperidin-1-yl]-propan-2-ol
EXAMPLE 123
1-[1-{2-Hydroxy-3-[4-(1H-pyrrolo[3,2-c]pyridin-3-yl)-piperidin-1-yl]-propyl}-3-(4-
trifluoromethyl-phenyl)-1,4,6,7-tetrahydro-pyrazolo[4,3-c]pyridin-5-yl]-ethanone
EXAMPLE 124
1-[3-(4-Bromo-phenyl)-5-methanesulfonyl-4,5,6,7-tetrahydro-pyrazolo[4,3-
c]pyridin-1-yl]-3-[4-{1H-pyrrolo[3,2-c]pyridin-3-yl)-piperidin-1-yl]-propan-2-ol
EXAMPLE 125
1-(3-(4-Bromo-phenyl)-1-{2-hydroxy-3-[4-(1H-pyrrolo[3,2-c]pyridin-3-yl)-
piperidin-1-yl]-propyl}-1,4,6,7-tetrahydro-pyrazolo[4,3-c]pyridin-5-yl)-ethanone
EXAMPLE 126
3-(1-{2-Hydroxy-3-[5-methanesulfonyl-3-(4-trifluoromethyl-phenyl)-4,5,6,7-
tetrahydro-pyrazolo[4,3-c]pyridin-1-yl]-propyl}-piperidin-4-yl)-5-oxy-pyrrolo[3,2-
c]pyridine-1-carboxylic acid methyl ester
EXAMPLE 128
3-(1-{3-[5-Acetyl-3-(4-trifluoromethyl-phenyl)-4,5,6,7-tetrahydro-
pyrazolo[4,3c]pyridin-1-yl]-2-hydroxy-propyl}-piperidin-4-yl)-6-fluoro-
benzofuran-2-carboxylic acid methyl ester
EXAMPLE 129
3-(1-{3-[5-Acetyl-3-(4-trifluoromethyl-phenyl)-4,5,6,7-tetrahydro-
pyrazolo[4,3c]pyridin-1-yl]-2-hydroxy-propyl}-piperidin-4-yl)-6-fluoro-
benzo[b]thiophene-2-carboxylic acid methyl ester

EXAMPLE 130
1-[4-{6-Fluoro-benzo[b]thiophen-3-yl)-pipericlin-1-yl]-3-[5-methanesulfonyl-3-
(4trifluoromethyl-phenyl)-4,5,6,7-tetrahydro-pyrazolo[4,3-c]pyridin-1-yl]-propan-
2-ol
EXAMPLE 131
1-[1-{3-[4-(6-Fluoro-benzofuran-3-yl)-pipericlin-1-yl]-2-hydroxy-propyl}-3-
(4trifluoromethyl-phenyl)-1,4,6,7-tetrahydro-pyrazolo[4,3-c]pyridin-5-yl]-
ethanone
EXAMPLE 132
6-Fluoro-3-(1-{2-hydroxy-3-[5-methanesulfonyl-3-(4-trifluoromethyl-phenyl)-
4,5,6,7-tetrahydro-pyrazolo[4,3-c]pyrilin-1-yl]-propyl}-piperidin-4-yl)-
benzo[b]thiophene-2-carboxylic acid
EXAMPLE 133
6-Fluoro-3-(1-{3-[5-methanesulfonyl-3-(4-trifluoromethyl-phenyl)-4,5,6,7-
tetrahydro-pyrazolo[4,3-c]pyridin-1-yl]-propyl}-piperidin-4-yl)-
benzo[b]thiophene-2-carboxylic acid dimethylamide
EXAMPLE 134
3-(1-{3-[5-Acetyl-3-(4-trifluoromethyl-phenyl)-4,5,6,7-tetrahydro-pyrazolo[4,3-
c]pyridin-1-yl]-2-hydroxy-propyl}-piperidin-4-yl)-6-fluoro-benzo[b]thiophene-2-
carbonitrile
EXAMPLE 135
6-Fluoro-3-(1-{2-hydroxy-3-[5-methanesulfonyl-3-(4-trifluoromethyl-phenyl)-
4,5,6,7-tetrahydro-pyrazolo[4,3-c]pyridin-1-yl]-propyl}-piperidin-4-yl)-
benzo[b]thiophene-2-carbonitriIe





F. Other Embodiments
The features and advantages of the invention are apparent to one of
ordinary skill in the art. Based on mis disclosure, including the summary,
detailed description, background, examples, and claims, one of ordinary skill in
the art will be able to make modifications and adaptations to various conditions
and usages. These other embodiments are also within the scope of the
invention.

We Claim
1.
A substituted pyrazoles compound of formula(I)

wherein:
the dashed line adjacent OR6 is absent or an sp2 bond;
Y is nitrogen or R20C;
Z is nitrogen or R21C;
T is nitrogen or R2C;
S is nitrogen or R3C;
provided between 0 and 3 of S, T, Y, and Z are nitrogen; and further
provided that one of S, T, Y, and Z can be =N+-O' where the remaining
three are not nitrogen;
R20 is selected from hydrogen, halogen, C1-5alkoxy, hydroxy, C1-5alkyl,
cyano, nitro, C1-5 haloalkyl, RoRPN, R°RPNC=O, C2-8acyl, 4-7 membered
heterocyclyl, (4-7 membered heterocyclyl)- C1-5 alkylene, phenyl,
(phenyl)C 1-5 alkylene. R14OC=O, R14S, R14SO, and R14SO2;
R21 is selected from hydrogen, halogen, C1-5alkoxy, hydroxy, C1-5alkyl,
cyano, nitro, C1-5 haloalkyl, RcRdN, RcRdNC=O, C2-8acyl, 4-7 membered
heterocyclyl, (4-7 membered heterocyclyl)-C 1-5 alkylene, phenyl,
(phenyl)C 1-5 alkylene, R15OC=O, R15S, R15SO and R15SO2;

R2 is selected from hydrogen, halogen, C1-5 alkoxy, hydroxy, C1-5 alkyl,
cyano, nitro, C1-5 haloalkyl, ReRfN, ReRfNC=O, C2-8acyl, 4-7 membered
heterocyclyl, (4-7 membered heterocyclyl)-C 1-5 alkylene, phenyl,
(phenyl)C 1-5 alkylene, R16OC=O, R16S, R16SO and R16SO2.
R3 is selected from hydrogen, halogen, C1-5 alkoxy, hydroxy, C1-5 alkyl,
cyano, nitro, C1-5 haloalkyl, R0RhN, C2-6 acyl, 4-7 membered heterocyclyl,
(4-7 membered heterocyclyl)- C 1-5 alkylene, phenyl, (phenyl)C 1-5
alkylene, R17OC=O, RmRnNC=O, RmR"NSO2, R17S, R17SO and R17SO2;
R5 and R6 are independently selected from hydrogen and C1-5 alkyl;
R7 and R8 independently are hydrogen, C1-5 alkyl, C1-5 alkenyl, C1-5 alkoxy, C1-5
alkylthio, halogen, or 4-7 membered carbocyclyl or heterocyclyl;
alternatively, R7 and R8 can be taken together to form an optionally
substituted 5- to 7- membered carbocyclic or heterocyclic ring, which
ring may be unsaturated or aromatic; said ring being optionally
substituted with between 1 and 3 substituents independently selected
from halo, hydroxy, cyano, nitro, amino, Rt, RtO-, RtS-, RtO(C 1-5
alkylene)-, RtO(C=O)-, Rt(C=O)-, Rt(C=S)-, Rt(C=O)O-, RtO(C=O)(C=O)-,
RtSO2, NHRU(C=NH)-, NHRUSO2-, and NHRU(C=O)-;
Rt is C 1-6 alkyl, phenyl, benzyl, phenethyl, or C 2-5 heterocyclyl, (C 1-5
heterocyclyl)C 1-6 alkylene, NH2, mono- or di(C 1-6 alkyl)N-, or R49OR50-,
wherein R49 is H, C 1-5 alkyl, C 2-5 alkenyl, phenyl, benzyl, phenethyl, C 1-5
heterocyclyl, or (C 1-5 heterocyclyl)C 1-6 alkylene and R50 is C 1-5 alkylene,
phenylene, or divalent C 1-5 heterocyclyl; and
Ru can be H in addition to the values for Rt;
Rc is hydrogen, C1-5 alkyl, phenyl, C 2-5 heterocyclyl, C 2-8 acyl, aroyl,
R10OC=O-, RiRjNC=O, R10SO-, R10SO2-, and RiRjNSO2;
Re is hydrogen, C1-5 alkyl, phenyl, C2-5 heterocyclyl, C 2-8 acyl, aroyl,
R40OC=O, R43R44NC=O, R40SO, R40SO2, and R43R44NSO2;
Rm is hydrogen, C1-5 alkyl, phenyl, C 2-5 heterocyclyl, C 2-8 acyl, aroyl,
R41OC=O, R45R46NC=O, R41SO, R41SO2, and R45R46NSO2;
R° is hydrogen, C1-5 alkyl, phenyl, C 2-5 heterocyclyl, C 2-8 acyl, aroyl,
R42OC=O, R47R48NC=O, R42SO, R42SO2, and R47R48NSO2;

each of Rd, Rf, Rn, and Rp is independently selected from hydrogen, C1-5 alkyl,
phenyl, and C 2-5 heterocyclyl; in addition, Rc and Rd, Re and Rf, Rm and
Rn, or R° and Rp, independently, can be taken together to form an
optionally substituted 4- to 7-membered heterocyclic ring, which ring
may be saturated, unsaturated or aromatic;
each of R9, R10, R11, R14, R15, R16, R17, R40, R41, and R42 is independently C1-5
alkyl, phenyl, or C 2-5 heterocyclyl;
each of Ri and Rf, Rk and Rl, R43 and R44, R45 and R46, R47 and R46 are
independently hydrogen, C1-5 alkyl, C3-5alkenyl, phenyl, or C 2-5
heterocyclyl; in addition, Ri and Rj, and Rk and Rj, R43 and R44, R45 and
R46, and R47 and R48, independently, can be taken together to form an
optionally substituted 4- to 7-membered heterocyclic ring, which ring
may be saturated, unsaturated or aromatic;
Rg is hydrogen, C1-5 alkyl, phenyl, or C 2-5 heterocyclyl, C 2-8 acyl, aroyl,
R9OC=O, R18R18NC=O, R9SO, R9SO2, or R18R19NSO2;
Rh is hydrogen, C1-5 alkyl, phenyl, or C 2-5 heterocyclyl;
alternatively, R° and Rh can be taken together to form an optionally
substituted 4- to 7- membered heterocyclic ring, which ring may be
saturated, unsaturated or aromatic;
R18 and R19 independently are hydrogen , C1-5 alkyl, phenyl, or C 2-5 heterocyclyl;
alternatively, R18 and R19 can be taken together to form an optionally
substituted 4- to 7- membered heterocyclic ring, which ring may be
saturated, unsaturated or aromatic;
n is 0, 1 or 2;
G is C3-6 alkenediyl or C3-6 alkanediyl, optionally substituted with hydroxy,
halogen, C1-5 alkyl, C1-5alkoxy, oxo, hydroximino, CO2Rk, NRkRl, (L)-C 1-4
alkylene-, RkRlNCO2, [(L)-C 1-5 alkylene]amino, N3, or (L)-C1-5 alkoxy;
L is amino, mono- or di-C1-5alkylamino, pyrrolidinyl, morpholinyl,
piperidinyl, homopiperidinyl, or piperazinyl, wherein available ring
nitrogens can be optionally substituted with C1-5 alkyl, benzyl, C2-5acyl, C
1-5 alkylsulfonyl, or C1-5 alkoxycarbonyl;
Ar represents a monocyclic or bicyclic aryl or heteroaryl ring, optionally
substituted with between 1 and 3 substituents independently selected

from halogen, C1-5alkoxy, C1-5 alkyl, C2-5alkenyl, cyano, azido, nitro,
R22R23N, R22S, R22SO, R22SO2, R22OC=O, R22R23NO=O, C1-5 haloalkyl, C1-
5 haloalkoxy, C1-5haloalkylthio, and C1-5 alkylthio;
R22 is hydrogen, C1-5 alkyl, C3-5alkenyl, phenyl, benzyl, C 2-5 heterocyclyl, C 2-8
acyl, aroyl, R11OC=O, R24R25NC=O, R11S, R11SO, R11SO2, or
R23 is hydrogen, C1-5 alkyl, phenyl, benzyl, or C 2-5 heterocydyl;
alternatively, R22 and R23 can be taken together to form an optionally
substituted 4- to 7-membered heterocyclic ring, which ring may be
saturated, unsaturated or aromatic;
R24 and R29 are independently hydrogen, C1-5 alkyl, phenyl, benzyl, or C 1-5
heteroaryl;
alternatively, R24 and R25 can be taken together to form ah optionally
substituted 4- to 7- membered carbocyclic or heterocydic ring, which
ring may be saturated, unsaturated or aromatic;
R32 is hydrogen, C1-5 alkyl, cyano, C1-5 hydroxyalkyl, C2-6 acyl, -(C=O)NRVRX,
CHO, or C1-5 alkoxycarbonyl, wherein each of Rv and Rx is independently
selected from H , C1-5 alkyl, C1-5 hydroxyalkyl, C1-5 heterocydyl, (C1-5
heterocydyl) C1-5 aikylene, C1-5 aminoalkylene, C3-8 acyloxy, CHO, C1-6
alkoxycarbonyl, and cyano;
Q is NR33, S, or O;
R33 represents hydrogen, C1-5 alkyl, phenyl, benzyl, phenethyl, C2-5
heterocydyl, (C2-5 heterocydyl)C 1-5 aikylene, C2-5 acyl, aroyl, R35OC=O,
R36R37NC=O, R35SO R35S R35SO2 and R36R37NSO2;
R35 is selected from hydrogen, C1-5 alkyl, phenyl, benzyl, phenethyl, and C 2-5
heteroaryl;
R36 and R37 are each independently selected from hydrogen, C1-5 alkyl, phenyl,
or C 2-5 heteroaryl;
alternatively, R36 and R37 can be taken together to form an optionally
substituted 4- to 7-membered ring heterocydic ring, which ring may be
saturated, unsaturated or aromatic;

wherein each of the above hydrocarbyl or heterocarbyi groups, unless
otherwise indicated, and in addition to any specified substituents, is
optionally and independently substituted with between 1 and 3
substituents selected from methyl, halomethyl, hydroxymethyl, halo,
hydroxy, amino, nitro, cyano, C 1-5 alkyl, C 1-5 alkoxy, -COOH, C 2-6 acyl,
[di(C 1-4 alkyl)amino]C 2-6 alkylene, [di(C 1-4 alkyl)amino] C 2-5 alkyl-NH-
CO-, and C1-5 haloalkoxy;
or a pharmaceutically acceptable salt, amide, or ester thereof, or a
stereoisomeric form thereof.
2. A compound as claim 1, wherein one of S, T, Y, and Z is nitrogen.
3. A compound as claim 1, wherein S and T are CR3 and CR2, respectively.
4. A compound as claim 1, wherein S, T, Y, and Z are CR3, CR2, CR20, and
CR21, respectively.
5. A compound as claim 1, wherein:
(a) Z is N, Y is N, S is CR3, and T is CR2; or
(b) S is N, T is N, Y is CR20, and Z is CR21.
6. A compound as claim 1, wherein R2 is hydrogen, halogen, C1-5 alkoxy,
cyano, ReRfN, or a 5-6 membered heterocyclyl.
7. A compound as claim 1, wherein R3 is hydrogen, halogen, C1-5 alkoxy,
C1-5 alkyl, cyano, R17OC=O, or R°RhN, where R° and Rhare H or C 1-5
alkyl, or are taken together to form a 5-6 membered heterocyclyl.
8. A compound as claim 1, wherein each of R2 and R3 is independently
selected from hydrogen, halogen, and a 5-6 membered heterocyclyl.

9. A compound as claim 1, wherein R5 and R6 are independently selected
from hydrogen and C1-3alkyl.
10. A compound of claim 9, wherein one of R5 and R6 is H.
11. A compound as claim 10, wherein R5 and R6 are each H.
12. A compound as claim 1, wherein one of R7 and R8 is H and the other is
5-7 membered carbocyclyl or heterocyclyl.
13. A compound as claim 1, wherein R7 and R8 are taken together to form an
optionally substituted 5- to 7- membered carbocyclic or heterocyclic ring.
14. A compound as claim 13, wherein R7 and R8 are taken together to form a
six-membered heterocyclyl.
15. A compound as claim 13 wherein R7 and R8 taken together form a 5-7
membered heterocyclyl optionally N-substituted with Rt(C=O)-, RtSO2-,
or NHRU(C=O)- wherein Rt is C 1-6 alkyl, phenyl, or C 2-5 heterocyclyl and
Ru is H, C 1-6 alkyl, phenyl, or C 2-5 heterocyclyl.
16. A compound as claim 1, wherein each of Rc, Re, Rm, and Rc is
independently selected from hydrogen, C1-5 alkyl, C2-8acyl, (C 1-5
alkyl)OC=O, and the respective RRNC=O, RSO, RSO2, and RRNSO2
groups.
17. A compound as claim 1, wherein each of Rc, Rd, Rg, Rh, R°, Rf, and Rp is
independently selected from hydrogen and C1-5alkyl; or, independently,
Re and Rf, R9 and Rh, or R° and Rp taken together form an optionally
substituted 4- to 7- membered carbocyclic or heterocyclic ring.
18. A compound as claim 17 wherein Re and Rf taken together are
morpholinyl, piperidinyl, or pyrrolidinyl.

19. A compound as claim 1, wherein each of R43, R44, R45, R46, R47, R48, Ri, Rj
Rk and Rl independently is hydrogen or C1-5 alkyl.
20. A compound as claim 1, wherein each of R8, R11, R14, R16, R16 and R17 is
independently C1-5 alkyl.
21. A compound ofclaim 1, wherein R° is C1-5 alkyl, C 2-6 acyl, R9OC=O,
R18R19NC=O, R9SO, R9SO2, or R18R19NSO2; and Rh is H or C1-5 alkyl;
alternatively, Rg and Rh can be taken together to form an optionally
substituted 5- to 6-membered heterocyclyl.
22. A compound as claim 21, wherein R° and Rh are each C 1-3 alkyl.
23. A compound as claim 1, wherein R18 and R19 independently are
hydrogen or C1-5 alkyl.
24. A compound as claim 1, wherein n is 1.
25. A compound as claim 1, wherein G is C3-4 alkanediyl, optionally
substituted with hydroxy, halogen, [(L)-C 1-5 alkylene]amino, or (L)-C1-5
alkyloxy.
26. A compound as claim 25, wherein G is C3 alkanediyl, optionally
substituted with hydroxy.
27. A compound as claim 1, wherein R20 and R21 are independently selected
from hydrogen, halogen, C1-5alkoxy, C1-5 alkyl, cyano, nitro, 4-7
membered heterocyclyl, and R°RPN or RcRdN, respectively.
28. A compound as claim 27, wherein R20 and R21 are independently
selected from hydrogen, halogen, 5- to 6-membered heterocyclyl, and
R°RpN or RcRdN, respectively.

29. A compound as claim 1, wherein Ar represents a monocydic ring,
optionally substituted with 1 to 2 substituents selected from halogen,
C1-5 alkyl, cyano, nitro, R22R23N, C1-3haloalkyl, and C1-3 haloalkoxy.
30. A compound as claim 29, wherein Ar is a six-membered aromatic ring
monosubstituted at the 4-position with halogen, methyl, CF3, or OCF3, or
disubstituted at the 3- and 4-positions with substituents independently
selected from halogen, CF3, methyl, and OCF3.
31. A compound as claim 29, wherein each of R22, R23, and R24 is
independently hydrogen or C1-5 alkyl.
32. A compound as claim 1, wherein R25 and R26 independently are
hydrogen or C1-5 alkyl,
or, alternatively, R25 and R26 are taken together to form an optionally
substituted 4- to 7- membered heterocyclic ring, which ring may be
saturated, unsaturated or aromatic.
33. A compound as claim 32, wherein R25 and R26 independently are
hydrogen or C1-5 alkyl.
34. A compound as claim 1, wherein Q is NR33 or S.
35. A compound as claim 34, wherein Q is NR33, R33 is H or C2-5heterocyclyl,
and R32 is H, C 1-5 alkyl, C1-5 hydroxyalkyl, -(C=O)NRVRX, CHO, or C 1-6
alkoxycarbonyl, wherein each of Rv and Rx is independently selected
from H, C 1-5 hydroxyalkyl, (C 1-5 heterocyclyl)-C 1-5 alkylene, and C 1-5
aminoalkylene.
36. A compound as claim 34, wherein Q is S and R33 is NR36R37(C=O)-
where each of R36 and R37 are independently selected from hydrogen
and C1-5 alkyl.

37. A compound as claim 1, wherein R35 is selected from hydrogen and
C1-5 alkyl; R36 and R37 are each independently selected from hydrogen,
C1-5 alkyl, or, alternatively, R36 and R37 can be taken together to form an
optionally substituted 4- to 7-membered heterocyclic ring.
38. A compound as claim 1, wherein
Y is nitrogen or R20C;
Z is nitrogen or R20C;
T is nitrogen or R2C;
S is nitrogen or R3C;
provided between 0 and 2 of S, T, Y, and Z are nitrogen;
R2 is hydrogen, halogen, hydroxy, C1-5 alkoxy, C1-5alkyl, 5- to 6-
membered heterocyclyl, or ReRfN;
R3 is hydrogen, halogen, C1-5 alkoxy, hydroxy, C1-5 alkyl, 5- to 6-
membered heterocyclyl, or RgRhN;
R5 and R6 are each H;
R7 and R8 independently are taken together to form an optionally substituted 5-
to 7- membered unsaturated heterocyclic ring;
each of Ra, Re, Rm, and R° is independently selected from hydrogen, C1-5alkyl,
C 2-8 acyt, (C1-5alkyl)OC=O, and the respective RRNC=O, RSO, RSO2,
and RRNSO2 groups;
each of Rb, Rf, Rn, and Rp, is independently selected from hydrogen and C1-5
alkyl;
each of R9, R11, R14, R15, R16, R17, R40, R41 and R42 is independently C1-5 alkyl;
each of Rc, Rd, Ri, Rj, R43, R44, R45, R46, R47, Rk and Rl are independently are
hydrogen or C1-5 alkyl;
Rg is hydrogen, or C1-5 alkyl, C 2-8 acyl, R9OC=O, R18R19NC=O, R9SO,
R9SO2, or R18R19NSO2;
Rh is hydrogen or C1-5 alkyl;
alternatively, Rg and Rh can be taken together to form an optionally
substituted 4- to 7- membered carbocyclic or heterocyclic ring, which
ring may be saturated, unsaturated or aromatic;

R18 and R19 independently are hydrogen or C1-5 alkyl;
n is o or 1;
G is C3-4 alkenediyl or C3-4 alkanediyl, optionally substituted with hydroxy,
halogen, C1-5alkyloxy, oxo, hydroximino, CO2Rk, RkRlNCO2, N3, or (L)-C1-
5alkoxy;
L is amino, mono- ordi-C1-5alkylamino, pyrrolidinyl, morpholinyl, piperidinyl
homopiperidinyi, or piperazinyl, available ring nitrogens being optionally
with C1-5 alkyl, benzyl, C2-5acyl, or C1-5alkyloxycarbonyl;
R20 and R21 are independently selected from hydrogen, halogen, C1-5alkoxy,
C1-5 alkyl, cyano, nitro, and R°RPN;
alternatively, R3 and R20 or R3 and R21 can be taken together to form an
optionally substituted 5- or 6-membered carbocyclic or heterocyclic ring,
which ring may be saturated, unsaturated or aromatic;
Ar represents a monocyclic or bicyclic aryl or heteroaryl ring, optionally
substituted with hydrogen, halogen, C1-51alkoxy, C1-5 alkyl, cyano, nitro,
R22R23N, R24SO2, R24OC=O, R25R26NC=O, CF3, OCF3, SCF3, or C1-5
alkylthio;
R22 is hydrogen, C1-5 alkyl, phenyl, benzyl, phenethyl, C2-5 heteroaryl, C2-8acyl,
aroyl, R24OC=O, R25R26NC=O, R24SO, R24SO2, or R25R26NSO2;
R23 is hydrogen or C1-5alkyl;
alternatively, R22 and R23 can be taken together to form an optionally
substituted 4- to 7- membered carbocyclic or heterocyclic ring, which
ring may be saturated, unsaturated or aromatic;
R24 is hydrogen or C1-5 alkyl;
R25 and R26 are independently hydrogen or C1-5 alkyl;
or, alternatively, R25 and R26 can be taken together to form an optionally
substituted 4- to 7- membered carbocyclic or heterocyclic ring, which
ring may be saturated, unsaturated or aromatic;
R32 is hydrogen, C1-5 alkyl, C1-5 hydroxyalkyl, CHO, C 2-6 acyl, C 1-6
alkoxycarbonyl, or -(C=O)NRVRX, wherein each of RVRX is independently
selected from H, C 1-5 alkyl, C1-5 hydroxyalkyl, C 3-6 acyloxy, (amino)C 1-6
alkylene, (C 1-5 heterocyclyl)C 1-5 alkylene, or C 1-5 alkoxycarbonyl;
Q is NR23 or S;

R33 represents hydrogen, C 1-5alky), phenyl, benzyl, (C 2-5 heterocydyl)C 1-5
alkylene, C 2-8 acyl, aroyl, R35OC=O, R36R37NC=O, R35SO2 and
R36R37NSO2;
R35 is selected from hydrogen and C1-5 alkyl;
R36 and R37 are each independently selected from hydrogen and C1-5 alkyl.
39. A compound as claim 1, wherein
one of R5 and R6 is H,
R7 and R6 are taken together to form an optionally substituted 6-
membered carbocyclic or heterocyclic ring; and
Ar represents a monocyclic ring, optionally substituted with 1 to 2
substituents selected from halogen, C1-5alkyl, cyano, nitro, R22R23N, CF3
and OCF3.
40. A compound as claim 39, wherein
both R5 and R6 are each H, and
Ar is a six membered ring substituted with halogen, CF3, methyl,
halomethyl, or OCF3, at the 3- or 4- position, or disubstituted at the 3-
and 4- positions.
41. A compound as claim 40, wherein R7 and R8 taken together form
pyridinyl, pyrimidinyl, or piperazinyl, optionally N-substituted with -
(C=O)Rt, SO2-Rt, or-(C=O)NHRu.
42. A compound as claim 39, wherein R22 and R23 taken together are
independently morpholinyl, piperidyl, or pyrrolidinyl, optionally
substituted.
43. A compound as claim 1, wherein the dashed line adjacent C-R6 is
absent.

44. A compound as claim 1, selected from:
1-{4-(5-Chloro-1H-indol-3-yl)-piperidin-1-yl]-3-[5-methanesulfonyl-3-(4-
trifluoromethyl-phenyl)-4,5,6,7-tetrahydro-pyrazolo[4,3-c]pyridin-1-yl]-propan-2-
ol;
1-{4-(7-Chloro-1H-indol-3-yl)-piperidin-1-yl]-3-[5-methanesulfonyl-3-(4-
trifluoromethyl-phenyl)-4,5,6,7-tetrahydro-pyrazolo[4,3-c]pyridin-1-yl]-propan-2-
ol;
1-[4-(5-Chloro-2-methyl-1H-indol-3-yl)-piperidin-1-yl]-3-[5-
methanesulfonyl-3-(4-trifluoromethy)-phenyl)-4,5,6,7-tetrahydro-pyrazolo[4,3-
c]pyridln-1-yl]-propan-2-ol;
1-{4-[6-Chloro-1-(2-morpholin-4-ylethyl)-1H-indol-3-yl]-piperidin-1-yl}-3-
[5-methanesulfonyl-3-(4-trifluoromethyl-phenyl)-4,5,6,7-tetrahydro-pyrazolo[4,3-
c]pyridin-1-yl]-propan-2-ol;
1-[5-Methanesulfonyl-3-(4-trifluoromethyl-phenyl)-4,5,6,7-tetrahydro-
pyrazolo[4,3-c]pyridin-1-yl]-3-[4-(1H-pyrrolo[3,2-c]pyridin-3-yl)-piperidin-1-yl]-
propan-2-ol;
1-[5-Methanesulfonyl-3-(4-trifluoromethyl-phenyl)-4,5,6,7-tetrahydro-
pyrazolo[4,3-c]pyridin-1-yl]-3-[1H-pyrrolo[2,3-b]pyridin-3-yl]-piperidin-1-yl]-
propan-2-ol;
1-[5-Methanesulfonyl-3-(4-trifluoromethyl-phenyl)-4,5,6,7-tetrahydro-
pyrazolo[4,3-c]pyridin-1-yl]-3-[4-(5-morpholin-4-yl-1H-pyrrolo[2,3-c]pyridin-3-yl)-
piperidin-1-yl]-propan-2-ol;
1 -[4-(6-Dimethylamino-1H-pyrrolo[3,2-c]pyridin-3-yl)-piperidin-1-yl]-3-[5-
methanesulfonyl-3-(4-trifluoromethyl-phenyl)-4,5,6,7-tetrahydro-pyrazolo[4,3-
c]pyridin-1-yl]-propan-2-ol;
1-[5-Methanesulfonyl-3-(4-trifluoromethyl-phenyl)-4,5,6,7-tetrahydro-
pyrazolo[4,3-c]pyridin-1-yl]-3-[4-(6-morpholin-4-yl-1H-pyrrolo[3,2-c]pyridin-3-yl)-
piperidin-1-yl]-propan-2-ol;
1-[5-Methanesulfonyl-3-(4-trifluoromethyl-phenyl)-4,5,6,7-tetrahydro-
pyrazolo[4,3-c]pyridin-1-yl]-3-[4-(6-morpholin-4-yl-5-oxy-1H-pyrrolo[3,2-
c]pyridin-3-yl)-piperidin-1-yl]-propan-2-ol;

6-Fluoro-3-(1-{3-[5-methanesulfonyl-3-(4-trifluoromethyl-phenyl)-4,5,6,7-
tetrahydro-pyrazolo[4,3-c]pyridin-1-yl]-propyl}-piperidin-4-yl)benzo[b]thiophene-
2-carboxylic acid (2-hydroxy-ethyl)-amide;
6-Fluoro-3-(1-{3-[5-methanesulfonyl-3-(4-trifluoromethyl-phenyl)-4,5,6,7-
tetrahydro-pyrazolo[4,3-c]pyridin-1-yl-propyl}-piperidin-4-yl)benzo[b]thiophene-
2-carboxylic acid (2-amino-ethyI)-amide; and
6-Fluoro-3-(1-{3-[5-methanesulfonyl-3-(4-trifluoromethyl-phenyl)-4,5,6,7-
tetrahydro-pyrazolo[4,3-c]pyridin-1-yl]-propyl}-piperidin-4-yl)benzo[b]thiophene-
2-carboxylic acid (2-morpholin-4-yl-ethyl)-amide.
45. A compound as claim 1, selected from:
1-[1-{1-Hyroxy-3-[4-(1H-inclol-3-yl)-piperidin-1-yl]-propyl}-3-(4-
trifluoromethyl-phenyl)-1,4,6,7-tetrahydro-pyrazolo[4,3-c]pyridin-5-yl]-ethanone;
1-[4-(5-Fluoro-1H-indol-3-yl)-piperidin-1-yl]-3-[5-methanesulfonyl-3-(4-
trifluoromethyl-phenyl)-4,5,6,7-tetrahydro-pyrazolo[4,3-c]pyridin-1-yl]-propan-2-
ol;
1-[3-(4-Bromo-phenyl)-5-methanesulfonyl-4,5,6,7-tetrahydro-
pyrazolo[4,3-c]pyridin-1-yl]-3-[4-(5-chloro-1H-indol-3-yl)-piperidin-1-yl]-propan-
2-ol;
1-[3-(4-Bromo-phenyl)-5-methanesulfonyl-4,5,6,7-tetrahydro-
pyrazolo[4,3-c]pyridin-1-yl]-3-[4-(5-chloro-2-methyl-1H-indol-3-yl)-piperidin-1-
yl]-propan-2-ol;
1-[5-Methanesulfonyl-3-(4-trifluoromethyl-phenyl)-4,5,6,7-tetrahydro-
pyrazolo[4,3-c]pyridin-1-yl]-3-[4-(5-methyl-1H-indol-3-yl)-piperidin-1-yl]-propan-
2-ol;
3-(1-{2-Hydroxy-3-[5-methanesulfonyl-3-(4-trifIuoromethyl-phenyl)-
4,5,6,7-tetrahydro-pyrazolo[4,3-c]pyridin-1-yl]-propyl}-piperidin-4-yl)-1H-indole-
5-carbonitrile;
1-[5-Methanesulfonyl-3-(4-trifluoromethyl-phenyl)-4,5,6,7-tetrahydro-
pyrazolo[4,3-c]pyridin-1-yI]-3-[4-(5-methoxy-1H-indol-3-yl)-piperidin-1-yl]-
propan-2-ol;

3-(1-{2-Hydroxy-3-{5-methanesulfonyl-3-(4-trifluoromethyl-phenyl)-
4,5,6,7-tetrahydro-pyrazolo[4,3-c]pyrldin-1-yr]-propyl}-piperidin-4-yl)-1H-indole-
5-carboxylic acid ethyl ester;
1-[4-(6-Chloro-1H-indol-3-yl)-piperidin-1-yl]-3-[5-methanesulfonyl-3-(4-
trifluoromethyl-phenyl)-4,5,6,7-tetrahydro-pyrazolo[4,3-c]pyridin-1-yl]-propan-2-
ol;
1-[1-(3-{4-[6-Chlolo-1-(2-morpholin-4-yl-ethyl)-1H-indol-3-yl]-piperidin-1 -
yl}-2-hydroxy-propyl)-3-(4-trifluoromethyl-phenyl)-1,4,6,7-tetrahydro-
pyrazolo[4,3-c]pyridin-5-yl]-ethanone;
1-[5-Methanesulfonyl-3-(4-trifiuoromethyl-phenyl)-4,5,6,7-tetrahydro-
pyrazolo[4,3-c]pyrklin-1-yl]-3-[4-(1H-pyrrolo[3,2-b]pyridin-3-yl)-piperidin-1-yl]-
propan-2-ol;
1-[5-Methanesulfonyl-3-(4-trifluoromethyl-phenyl)-4,5,6,7-tetrahydro-
pyrazolo[4,3-c]pyridin-1-yl]-3-{4-(1H-pyrrolo[2,3-c]pyridin-3-yl)-piperidin-1-yl]-
propan-2-ol;
1-[5-MethanesuIfonyl-3-(4-trifluoromethyl-phenyl}-4,5,6,7-tetrahydro-
pyrazolo[4,3-c]pyridin-1-yl]-3-[4-(5-oxy-1H-pyrrolo[3,2-c]pyridin-3-yl)-piperidin-
1-yl]-propan-2-ol;
1-[4-(5-Dimethylamino-1H-pyrrolo[3,2-b]pyridin-3-yl)-piperidin-1-yl]-3-[5-
methanesulfonyl-3-(4-trifluoromethyl-phenyl)-4,5,6,7-tetrahydro-pyrazolo[4,3-
c]pyridin-1-yl]-propan-2-ol;
1-[4-(5-Dimethylamino-1H-pymolo[2,3-c]pyridin-3-yl)-piperidin-1-yl]-3-[5-
methanesulfonyl-3-(4-trifluoromethyl-phenyl)-4,5,6,7-tetrahydro-pyrazolo[4,3-
c]pyridin-1-yl]-propan-2-ol;
3-(1-{2-Hydroxy-3-[5-methanesulfonyl-3-(4-trifluoromethyl-phenyl)-
4,5,6,7-tetrahydro-pyrazolo[4,3-c]pyridin-1-yl]-propyl}-piperidin-4-yl)-1H-
pyrrolo[2,3-b]pyridine-6-carbonitrile;
1-[5-Methanesulfonyl-3-(4-trifluoromethyl-phenyl)-4,5,6,7-tetrahydro-
pyrazolo{4,3-c]pyridin-1-yl]-3-{4-[1-(2-morpholin-4-yl-ethyl)-1H-pyrrolo[2,3-
b]pyridin-3-yl]-piperidin-1-yl}-propan-2-ol;
1-[5-Methanesulfonyl-3-(4-trifluoromethyl-phenyl)-4,5,6,7-tetrahydro-
pyrazolo[4,3-c]pyridin-1-yl]-3-[4-(7-morpholin-4-yl-1H-pyrrolo[2,3-c]pyridin-3-yl)-
piperidin-1-yI]-propan-2-ol;

1-[4-(4-Fluoro-2-hydroxymethyl-benzo[b]thiophen-3-yl)-piperidin-1-yl]-3-
[5-methanesulfonyl-3-(4-trifluoromethyl-phenyl)-4,5,6,7-tetrahydro-pyrazolo[4,3-
c]pyridin-1-yl]-propan-2-ol;
6-Fluoro)-3-(1-{2-hydroxy-3-[5-methanesulfonyl-3-(4-trifluoromethyl-
phenyl)-4,5,6,7-tetrahydro-pyrazolo[4,3-c]pyridin-1-yl]-propyl}-piperidin-4-yl)-
benzo[b]thiophene-2-carbaldehyde;
6-Fluoro-3-(1-{2-hydroxy-3-[5-methanesulfonyl-3-(4-trifluoromethyl-
phenyl)-4,5,6,7-tetrahydro-pyrazolo[4,3-c]pyridin-1-yl]-propyl}-piperidin-4-yl)-
benzo[b]thiophene-2-carboxylic add methyl ester;
6-Fluoro-3-(1-{3-[5-methanesulfonyl-3-(4-trifluoromethyl-phenyl)-
4,5,6,7-tetrahydro-pyrazolo[4,3-c]pyridin-1-yl-propyl}-piperidin-4-
yl)benzo[b]thiophene-2-carboxylic acid amide;
and 6-Fluoro-3-(1-{3-[5-methanesulfonyl-3-(4-trifluoromethyl-phenyl)-
4,5,6,7-tetrahydro-pyrazolo[4,3-c]pyridin-1-yl]-propyl}-piperidin-4-
yl)benzo[b]thtophene-2-carboxylic acid ethylamide.
46. A compound as claim 1, selected from:
1-{4-[6-Chloro-1 -(2-morpholin-4-yl-ethyl)-1H-indol-3-yl-piperidin-1-yl}-3-
[5-methanesutfonyl-3-(4-trifluoromethyl-phenyl)-4,5,6,7-tetrahydro-pyrazolo[4,3-
c]pyridin-1-yl]-propan-2-ol;
6-Fluoro-3-(1-{3-[5-methanesulfonyl-3-(4-trifluoromethyl-phenyl)-4,5,6,7-
tetrahydro-pyrazoto[4,3-c]pyridin-1-yl]-propyl}-piperidin-4-y))benzo[b]thiophene-
2-carboxylic acid (2-morpholin-4-yl-ethyl)-amide;
1-[5-Methanesulfonyl-3-(4-trifluoromethyl-phenyl)-4,5,6,7-tetrahydro-
pyrazolo[4,3-c]pylidin-1-yl]-3-[4-(5-oxy-1H-pyrrolo[3,2-c]pyridin-3-yl)-piperidin-
1-yl]-propan-2-ol; and
1-[5-Methanesulfonyl-3-(4-trifluoromethyl-phenyl)-4,5,6,7-tetrahydro-
pyrazolo[4,3-c]pyridin-1-yl]-3-(4-(6-morpholin-4-yl-1H-pyrrolo[3,2-cJpyridin-3-yl)-
piperidin-1-yl]-propan-2-ol.
47. A compound as claim 1, selected from:
1-(3-(4-Chioro-3-methyl-phenyl}-1-{2-hydroxy-3-[4-(1H-indol-3-yl)-
piperidin-1-yl]-propyl}-1,4,6,7-tetrahydro-pyrazolo[4,3-c]pyridin-5-yl)-ethanone;

1-[1-[3-{4-(5-Chloro-1H-indol-3-yl)-piperidin-1-yl]-2-hydroxy-propyl}-3-(4-
trifluoromethyl-phenyl))-1,4,6,7-tetrahydro-pyrazolo[4,3-c]pyridin-5-yl]-ethanone;
1-{3-[4-(5-Chloro-1H-indol-3-yl)-piperidin-1-yl]-propyl}-5-
methanesulfonyl-3-(4-trifluoromethyl-phenyl)-4,5,6,7-tetrahydro-1H-
pyrazolo[4,3-c}pyridine;
3-(1-{2-Hydroxy-3-[5-methanesulfonyl-3-(4-trifluoromethyl-phenyl)-
4,5,6,7-tetrahydro-pyrazolo[4,3-c]pyridin-1-yl]-propyl}-piperidin-4-yl)-1H-indole-
5-carbonitrile;
1-[4-{6-Chloro-1-methyl-1H-indol-3-yl)-piperidin-1-yl]-3-[5-
methanesulfonyl-3-(4-trifluoromethyl-phenyl)-4,5,6,7-tetrahydro-pyrazolo[4,3-
c]pyridin-1-yl]-propan-2-ol;
1-[4-(6-Chtoro-1-methanesulfonyl-1H-indol-3-yl)-piperidin-1-yl]-3-[5-
methanesulfonyl-3-(4-trifluoromethyl-phenyl)-4,5,6,7-tetrahydro-pyrazolo[4,3-
c]pyridin-1-yl]-propan-2-ol;
1-[3-(4-Bromo-phenyl)-5-methanesulfonyl-4,5,6,7-tetrahydro-
pyrazolo[4,3-c]pyridin-1-yl]-3-[4-(7-chloro-1H-indol-3-yl)-piperidin-1-yl]-propan-
2-ol;
3-(H3-[3-(4-Bromo-phenyl)-5-methanesulfonyl-4,5,6,7-tetrahydro-
pyrazolo[4,3-c]pyridin-1 -yl]-2-hydroxy-propyl}-piperidin-4-yl)-1H-indole-5-
carbonltrile;
1-[3-(4-Bromo-phenyl)-5-methanesulfonyl-4,5,6,7-tetrahydro-
pyrazolo[4,3-c]pyridin-1-yl]-3-{4-[6-chloro-1-(2-morpholin-4-yl-ethyl)-1H-indol-3-
yl]-piperidin-1-yl}-propan-2-ol;
1-[3-(4-Bromo-phenyl)-1-(3-{4-[6-chloro-1-(2-morpholin-4-yl-ethyl)-1H-
indol-3-yl]-piperidin-1-yl}-2-hydroxy-propyl)-1,4,6,7-tetrahydro-pyrazolo[4,3-
c]pyridin-5-yl]-ethanone;
1-[1-{2-Hydroxy-3-[4-(1H-pymolo(2,3-b]pyridin-3-yl)-piperidin-1-yl]-
propyl}-3-(4-trifluoromethyl-phenyl)-1,4,6,7-tetrahydro-pyrazolo[4,3-c]pyridin-5-
yl]-ethanone;
1-[3-(4-Bromo-phenyl)-5-methanesulfonyl-4,5,6,7-tetrahydro-
pyrazolo[4,3-c]pyridin-1-yl]-3-[4-(1H-pyrrolo[2,3-b]pyridin-3-yl)-piperidin-1-y)}-
propan-2-ol;

1-(3-(4-Bromo-phenyl)-1-{2-hydroxy-3-[4-(1H-pyrrolo[2,3-b]pyridin-3-yl-
piperidin-1-yl]-propyl}-1,4,6,7-tetrahydro-pyrazolo[4,3-c]pyridin-5-yl)-ethanone;
1-[1-(2-Hydroxy-3-{4-[1-(2-morpholin-4-yl-ethyl)-1H-pyrrolo[2,3-b]pyridin-
3-yl]-piperidin-1-yl}-propyl)-3-(4-trifluoromethyl-phenyl)-1,4,6,7-tetrahydro-
pyrazolo[4,3-c]pyridin-5-yl]-ethanone;
5-Methanesulfonyl-1-{3-[4-(1H-pyrrolo[2,3-b]pyridin-3-yl)-3,6-dihydro-2H-
pyridin-1-yl]-propyl}-3-(4-trifluoromethyl-phenyl)-4,5,6,7-tetrahydro-1H-
pyrazolo[4,3-c]pyridine; and
5-Methanesulfonyl-1-{3-[4-(1H-pyrrolo[2,3-b]pyridin-3-yl)-piperidin-1-yl]-
propyl}-3-(4-trlfluoromethyl-phenyl)-4,5,6,7-tetrahydro-1H-pyrazolo[4,3-
c]pyridine.
48. A compound as claim 1, selected from:
1-[3-{4-Bromo-phenyl)-5-methanesulfonyl-4,5,6,7-tetrahydro-
pyrazolo[4,3-c]pyridin-1-yl]-3-{4-[1-(2-morpholin-4-yl-ethyl)-1H-pyrrolo[2,3-
b]pyridin-3-yl]-piperidln-1-yl}-propan-2-ol;
1-[3-(4-Bromo-phenyl)-1-(2-hydroxy-3-{4-[1-(2-morpholin-4-yl-ethyl)-1H-
pyrrolo[2,3-b]pyridin-3-yl]-plperidin-1-yl}-propyl)-1,4,6,7-tetrahydro-
pyrazolo[4,3-c]pyridin-5-yl]-ethanone;
6-Chloro-3-(1-{2-hydroxy-3-[5-methanesulfonyl-3-(4-trifluoromethyl-
phenyl)-4,5,6,7-tetrahydro-pyrazolo[4,3-c]pyridln-1-yl]-propyl}-plperldln-4-yl)-
pyrrolo[2,3-b]pyridine-1-carboxylic acid methyl ester;
1 -[4-(6-Chloro-1H-pyrrolo[2,3-b]pyridin-3-yl)-piperidin-1-yl]-3-[5-
methanesulfonyl-3-(4-trifluoronnethyl-phenyl)-4,5,6,7-tetrahydro-pyrazolo[4,3-
c]pyridin-1-yl]-propan-2-ol;
1-[5-Methanesulfonyl-3-(4-trifluoromethyl-phenyl)-4,5,6,7-tetrahydro-
pyrazolo[4,3-c]pyridin-1-yl]-3-[4-(7-oxy-1H-pyrrolo[2,3-b]pyridin-3-yl)-piperidin-
1-yl]-propan-2-ol;
1-[5-Methanesulfonyl-3-(4-trifluoromethyl-phenyl)-4,5,6,7-tetrahydro-
pyrazolo[4,3-c]pyridin-1-yl]-3-[4-(6-morpholin-4-yl-1H-pyrrolo[2,3-b]pyridin-3-yl)-
piperidin-1-yl]-propan-2-ol;

1-[1-{2-Hydroxy-3-[4-(1H-pyrrolo[3,2-c]pyridin-3-yl)-piperidin-1-yl]-
propyl}-3-(4-trifluoromethyl-phenyl)-1,4,6,7-tetrahydro-pyrazolo[4,3-c]pyridin-5-
yl]-ethanone;
1-[3-(4-Bromo-phenyl)-5-methanesulfonyl-4,5,6,7-tetrahydro-
pyrazolo[4,3-c]pyridin-1-yl]-3-[4-(1H-pyrrolo[3,2-c]pyridin-3-yl)-piperidin-1-yl]-
propan-2-ol;
1-(3-(4-Bromo-phenyl)-1-{2-hydroxy-3-{4-(1H-pyrrolo[3,2-c]pyridin-3-yl)-
piperidin-1-yl]-propyl}-1,4,6,7-tetrahydro-pyrazolo[4,3-c]pyridin-5-yl)-ethanone;
3-(1-{2-Hydroxy-3-[5-methanesulfonyl-3-(4-trifluoromethyl-phenyl)-
4,5,67-tetrahydro-pyrazolo[4,3-c]pyridin-1-yl]-propyl}-piperidin-4-yl)-5-oxy-
pyrrolo[3,2-c]pyridine-1-carboxylic acid methyl ester,
3-(1-{3-[5-Acetyl-3-(4-trifluoromethyl-phenyl)-4,5,6,7-tetrahydro-
pyrazolo[4,3-c]pyridin-1-yl]-2-hydroxy-propyl}-piperidin-4-yl)-6-fluoro-
benzofuran-2-carboxylic acid methyl ester,
3-(1-{3-[5-Acetyl-3-(4-trifluoromethyl-phenyl)-4,5,6,7-tetrahydro-
pyrazolo[4,3c]pyridin-1-yl]-2-hydroxy-propyl}-piperidin-4-yl)-6-fluoro-
benzo[b]thtophene-2-carboxylic acid methyl ester;
1-[4-(6-Fluoro-benzo[b]thiophen-3-yl)-piperidin-1-yl]-3-[5-
methanesulfonyl-3-(4trifluoromethyl-phenyl)-4,5,6,7-tetrahydro-pyrazolo[4,3-
c]pyridin-1-yl]-propan-2-ol;
1-[1-{3-[4-(6-Fluoro-benzofuran-3-yl)-piperidin-1-y1]-2-hydroxy-propyl}-3-
(4trifluoromethyl-phenyl)-1,4,6,7-tetrahydro-pyrazolo[4,3-c]pyridin-5-yl]-
ethanone;
6-Fluoro-3-(1-{2-hydroxy-3-[5-methanesulfonyl-3-(4-trifluoromethyl-
phenyl)-4.5,6,7-tetrahydro-pyrazolo[4,3-c]pyridin-1-yl]-propyl}-piperidin-4-yl)-
benzo[b]thiophene-2-carboxylic acid;
6-Fluoro-3-(1-{3-[5-methanesulfonyl-3-(4-trifluoromethyl-phenyl)-4.5.6,7-
tetrahydro-pyrazolo[4,3-c]pyridin-1-yl]-propyl}-piperidin-4-yl)-
benzo[b]thbphene-2-carboxylic acid dimethylamide;
3-(1-{3-[5-Acetyl-3-(4-trifluoromethyl-phenyl)-4,5,6I7-tetrahydro-
pyrazolo[4,3-c]pyridin-1-yl]-2-hydroxy-propyl}-piperidin-4-yl)-6-fluoro-
benzo[b]thiophene-2-carbonitrile; and

6-Fluoro-3-(1-{2-hydraxy-3-[5-methanesulfonyl-3-(4-
trifluoromethyl-phenyl)-4, 5, 6, 7-tetrahydro-pyrazdo [4, 3-c]
pyridirhl-yl]-propyl)-plperldin-4-yl)- benzo [b] thiophene-2-
carbonitrile.
49. A pharmaceutical composition, comprising a compound of claim
1, 38, 44, 45, or 46 and a pharmaceutically acceptable carrier.
Substituted pyrazoles, methods of manufacturing them, compositions
containing them, and methods of using them to treat, for example,
autoimmune diseases mediated by cathepsin S are described.

Documents:

191-KOLNP-2003-FORM-27.pdf

191-kolnp-2003-granted-abstract.pdf

191-kolnp-2003-granted-assignment.pdf

191-kolnp-2003-granted-claims.pdf

191-kolnp-2003-granted-correspondence.pdf

191-kolnp-2003-granted-description (complete).pdf

191-kolnp-2003-granted-examination report.pdf

191-kolnp-2003-granted-form 1.pdf

191-kolnp-2003-granted-form 18.pdf

191-kolnp-2003-granted-form 2.pdf

191-kolnp-2003-granted-form 26.pdf

191-kolnp-2003-granted-form 3.pdf

191-kolnp-2003-granted-form 5.pdf

191-kolnp-2003-granted-reply to examination report.pdf

191-kolnp-2003-granted-specification.pdf

191-kolnp-2003-granted-translated copy of priority document.pdf


« Previous Patent
Next Patent »
Patent Number 225644
Indian Patent Application Number 191/KOLNP/2003
PG Journal Number 47/2008
Publication Date 21-Nov-2008
Grant Date 19-Nov-2008
Date of Filing 14-Feb-2003
Name of Patentee ORTHO MCNEIL PHARMACEUTICAL INC.
Applicant Address ROUTE 202, P. O. BOX 300, RARITAN NJ
Inventors:
# Inventor's Name Inventor's Address
1 MEDUNA STEVEN P. 9975 PASEO MONTRIL, SAN DIEGO CA 92111
2 PIO BARBARA A. 3898 ASHFORD STREET, SAN DIEGO, CA 92111
3 EDWARDS JAMES P. 8723 HESBY COURT, SAN DIEGO, CA 92129
4 CAI HUI 11213 CORTE BELLEZA, SAN DIEGO, CA 92130
5 WEI JIANMEI 12516 SEN DA PANACEA, SAN DIEGO, CA 92129
PCT International Classification Number C07D 471/04
PCT International Application Number PCT/US01/25180
PCT International Filing date 2001-08-10
PCT Conventions:
# PCT Application Number Date of Convention Priority Country
1 60/225,178 2000-08-14 U.S.A.