Indian Patents
Title of Invention

A PROCESS FOR THE PREPARATION OF 4, 5-DIAMINO SHIKIMIC ACID DERIVATIVE OF FORMULA IA
Abstract The present invention relates to a multistep synthesis for the preparation of 4, 5-diamino shikimic acid derivatives of formula starting from am isophthalic acid derivative of formula 4,5-Diamino shikimic acid derivatives are potent inhibitors of viral neuraminidase.
Full Text The present invention relates to a multi step process for the preparation of 4,5-diamino shikimic acid derivatives, especially for the preparation of (3R,4R,5S)-4-acetamido-5-amino-3-(l-ethylpropoxy)-l-cyclohexene-l-carboxylic acid ethylester and its pharmaceutically acceptable addition salts starting from isophthalic acid derivatives," individual process steps thereof, as well as new specific intermediates.
4,5-diamino shikimic acid derivatives, especially the (3R,4R,5S)-4-acetamido-5-amino-3-(l-ethylpropoxy)-l-cyclohexene-l-carboxylic acid ethylester and its pharmaceutically acceptable addition salts are potent inhibitors of viral neuraminidase ( J.C.Rohloff et al., J.Org.Chem., 1998, 63, 4545-4550; WO 98/07685).
A multi step synthesis of (3R,4R,5S)-4-acetamido-5-amino-3-(l-ethylpropoxy)-l-cyclohexene-1-carboxylic acid ethylester from (-)-quinic acid or (-)-shikimic acid is described in (J.C.Rohloff et al, loc.cit.).
Both (-)-quinic acid and (-)-shikimic acid are starting compounds which are rather expensive and hardly accessible in technical quantities. A multi step synthesis capable to run on a technical scale should therefore preferably be based on starting compounds which are more attractive in price and available in technical quantities.
Object of the present invention therefore is to provide such a new access to the 4,5-diamino shikimic acid derivatives mentioned above in good yields and excellent quality.

It was found that with the synthesis according to claim 1 this object could surprisingly be achieved.
/The present invention therefore relates to a process for the preparation of a 4,5-diamino shikimic acid derivative of formula

and pharmaceutically acceptable addition salts thereof
wherein R1 is an optionally substituted alkyl group,
R2 is an alkyl group and
R3 and R4, independent of each other are H or a substituent of an amino group, with
the proviso that both R3 and R4 are not H
and which is characterized in that in step a)
an isophtalic acid derivative of the formula


wherein R1 and R2 are as above and R5 is H or lower alkyl is hydrogenated to form an all-cis-cyclohexane dicarboxylate of the formula

wherein R", R and R are as above,
in step b)
the cyclohexane dicarboxylate of formula (III) is, if R5=H, selectively hydrolyzed to form the (S)- or (R)-cyclohexane monoacid of formulas IVa or IVb or, if R5=lower alkyl, either dealkylated first and then selectively hydrolyzed or selectively hydrolyzed first and then dealkylated to form the (S)- or (R)-cyclohexane mono acid of the formulas


wherein R and R are as above, in step c)
the cyclohexane monoacid of the formula (IVa) is further converted to an oxazohdinone of the formula

wherein R and R are as above,
in step d)
the oxazohdinone of formula (V) is transformed into a cyclohexenol of the formula

wherein R1 and R2 are as above and R6 is an amino protecting group

in step e)
the cyclohexenol of formula (VI) is further converted into an azide of formula

wherein R", R and R^ are as above,
in step f)
the azide of formula (VII) is reduced and acylated to form the acylated amine of the formula


wherein R1 R2 R3 R4 and R5 are as above, and in step g)
the acylated amine of the formula (VIII) is finally transferred into the 4,5-diamino shikimic acid derivative of formula (I) by removing the amino protecting group R and if necessary by forming the respective pharmaceutically acceptable salt.
The term alkyl in R" has the meaning of a straight chained or branched alkyl group of 1 to 20 C-atoms, expediently of 1 to 12 C-atoms. Examples of such alkyl groups are methyl, ethyl, n-propyl, i-propyl, n-butyl, i-butyl, tert.-butyl, pentyl and its isomers, hexyl and its isomers, heptyl and its isomers, octyl and its isomers, nonyl and its isomers, decyl and its isomers, undecyl and its isomers and dodecyl and its isomers.
This alkyl group can be substituted with one or more substituents as defined in e.g. WO 98/07685. Suitable substituents are alkyl of 1 to 6 C-atoms (as defined above), alkenyl of 2 to 6 C-atoms, cycloalkyl with 3 to 6 C-atoms, hydroxy, alkoxy with 1 to 6 C-atoms, alkoxycarbonyl with 1 to 6 C-atoms, F, CI, Br, and J. Preferred meaning for R"is 1-ethylpropyl.
R is a straight chained or branched alkyl group of 1 to 12 C-atoms, expediently of 1 to 6 C-atoms as exemplified above.
Preferred meaning for R is ethyl.
R5 is a lower n-alkyl group of 1 to 3 C-atoms, preferably methyl.
R3 and R4 is a substituent of an amino group conventionally used and known in the art and described e.g. in WO 98/07685.
R3 and R4 preferably stand for alkanoyl groups, more preferably lower alkanoyl with 1 to 6 C-atoms such as hexanoyl, pentanoyl, butanoyl (butyryl), propanoyl (propionyl), ethanoyl (acetyl) and methanoyl (formyl). Preferred alkanoyl group and therefore preferred meaning for R3 is acetyl and for R4" is H.

R^ is a common amino protecting group conventionally used and known in the art and described e.g. in "Protective Groups in Organic Chemistry", Theodora W. Greene et al., John Wiley & Sons Inc., New York, 1991, 315-385.
R^ suitably is benzyloxycarbonyl (Z), tert.-butyloxycarbonyl (BOG), allyloxycarbonyl (Alloc) or 9-fluorenylmethoxycarbonyl (FMOC), preferably tert.-butoxycarbonyl (BOG).
Preferred 4,5-diamino shikimic acid derivative of formula (I) is the (3R,4R,5S)-4-acetamido-5-amino-3-(l-ethylpropoxy)-l-cyclohexene-l-carboxyIic acid ethylester and the (3R,4R,5S)-4-acetamido-5-amino-3-(l-ethylpropoxy)-l-cyclohexene-l-carboxyric acid ethyl ester phosphate (1:1).
Provided that the process from step c) onwards is run with the cyclohexane monoacid of the formula (IVb) the process of the present invention allows to produce the (+)-enantiomer of the 4,5-dimino shikimic acid derivative having the formula

wherein R^ R^ R^ and R^ are as above and all the (+)-enantiomers of the corresponding intermediates.
Step a)
Step a) comprises the hydrogenation of an isophtalic acid derivative of the formula (II) to an all-cis- cyclohexane dicarboxylate of the formula (III).

Hydrogenation takes place with hydrogen in the presence of a common hydrogenation catalyst which may be applied on an inert support. Suitable hydrogenation catalysts are rhodium or ruthenium applied in an amount of 1 to 10% on an inert support, such as on aluminium oxide or charcoal.
The hydrogenation can be effected in an inert solvent like ethylacetate, ethanol, tetrahydrofuran or tert.-butyl methyl ether at temperatures between 20°C and 150°C and at hydrogen pressures between 1 bar and 200 bar .
The resulting cydohexane dicarboxylate of the formula (III) shows an all-cis meso form and therefore is optically inactive.
Step b)
Step b) comprises a selective enzymatic hydrolysis and, if necessary, a dealkylation of the cydohexane dicarboxylate of the formula (III) to either the (S)- or (R)-cydohexane mono acid of the formulas (IVa) or (IVb).
Starting from the cydohexane dicarboxylate of formula (III) with R =H selective enzymatic hydrolysis can directly take place, however, starting from the cydohexane dicarboxylate of formula (III) with R^=lower alkyl dealkylation can either take place before or after the selective hydrolysis.
The dealkylation, can take place with an alkali iodide in the presence of a trialkylhalogen silane. Dealkylation preferably is a demethylation and preferably sodium iodide together with trimethylchlorosilane is used.
This dealkylation as a rule is performed in an inert solvent, such as in acetonitril at temperatures between 20°C and 80 °C.

Selective hydrolysis comprises an enzymatic hydrolysis of the cyclohexane dicarboxylate of the formula (III), whereby the choice of the enzyme determines whether the (S)-monoacid of the formula

or the (R)-monoacid isomer of the formula

can be obtained.
In order to achieve the 4,5-diamino shikimic acid of formula (la) with the desired stereo configuration the subsequent reaction steps have to be performed with the (S)-monoacid of formula (IVa).
Starting with the all-cis-cyclohexane dicarboxylate of formula III with R = H suitable enzymes to gain the (S)-isomer of formula (IVa) are esterases of the EC class 3.1.1.1, preferably mammalian esterases (e.g. from pig, bovine or horse). The most preferred

enzyme is pig liver esterase (which is subsequently termed PLE). Commercial preparations ofPLE can be purchased e.g. from Roche Diagnostics, Fluka, Sigma, Amano or Altus. Also less purified PLE preparations (e.g. "PLE technical grade" from Roche Diagnostics) or only poorly purified preparations (e.g. such as "pig liver acetone powder" from Fluka) can be used as well as PLE preparations with enriched or separated isozyme fractions (like e.g. Chirazyme E-1 or Chirazyme E-2 from Roche Diagnostics).
As a common alternative the enzymes may be used in immobilized form.
The substrate is applied as a suspension in an aqueous solution in a 5 - 15% concentration (w/w), preferably around 10%. A suitable reaction temperature is room temperature to 35°C, a suitable reaction pH between 6.5 and 8.5.
As to the aqueous phase, common buffer solutions known to be used for biochemical conversions are used like e.g. phosphate or Tris-buffer in a concentration of 5 - 50 mM. Such a buffer solution can additionally contain a salt like e.g. NaCl or KCl in a concentration of 50 to 300 mM. A preferred buffering system could e.g. contain 0.1 M KCl and 10 mM Tris-hydrochloride pH 8.0.
After addition of the enzyme the pH of the reaction mixture is maintained under stirring at the selected value by the controlled addition of a base such as NaOH or KOH, whereby the formed monoacid goes into solution and the reaction mixture becomes rather clear.
After termination of the reaction, the product is worked up conventionally by acidification of the reaction mixture and extraction with a common organic solvent.
Starting with the all-cis cyclohexane dicarboxylate of formula 111 with R = H or lower alkyl, preferably methyl, suitable enzymes to gain the (R)-isomer of formula (IVb) are lipases of the EC class 3.1.1.3. Suitable representatives of this class are the lipases from Aspergillus oryzae (commercially available at Fluka), Thermomyces lanuginosa (formerly termed Humicola lanuginosa; e.g. from Novo Nordisk) and from Mucor miehei (e.g. from Novo Nordisk). Again, also less purified crude enzyme preparations maybe used.
Again, as a common alternative, the enzymes may be used in immobilized form.
The reaction is carried out in an aqueous or an aqueous-organic biphasic system. Preferred is a biphasic system with a water-immiscible apolar solvent as co-solvent. Suitable co-solvents are alkanes or cycloalkanes, preferred is cyclohexane.

The substrate is applied (as a suspension) in the mono- or biphasic system in 5 - 10 % overall concentration (w/w). A suitable reaction temperature is room temperature to 35°C, a suitable reaction pH between 6.5 and 8.5.
As to the aqueous phase, common buffer solutions known to be used for biochemical conversions are used like e.g. phosphate, borate or Tris-buffer in a concentration of 5 - 50 mM. Such a buffer solution can additionally contain a salt like e.g. NaCl, KCl or a polyhydric alcohol such as a sugar (e.g. glucose) in a concentration of 50 to 300 mM. A preferred buffering system could e.g. contain 0.1 M glucose and 5 mM sodium phosphate pH 7.0.
The ratio organic solvent / aqueous phase is in the range of 1:10 to 1:1.
After addition of the enzyme the pH of the reaction mixture is maintained under stirring at the selected value by the controlled addition of a base such as NaOH or KOH.
After termination of the reaction, the product is worked up conventionally by acidification of the reaction mixture and extraction with a common organic solvent.
Step c)
Step c) comprises the conversion of the cyclohexane mono acid of the formula (IVa) into the oxazolidinone of formula (V).
This conversion can take place applying the known principles of a Curtius or of a Hoffmann degradation. Where in the Hofmann degradation the oxazolidinone is formed by transformation of the cyclohexane monoacid into the respective cyclohexane monoamide and by subsequent ring formation e.g. with a hyprochlorite, the Curtius degradation involves the formation of the cyclohexane azide intermediate.
As a suitable variation of the Curtius degradation a Yamada-Curtius degradation using dialkylphosphorylazides or diarylphosphoryl azides, preferably diarylphosphoryl azides, most preferably diphenyl phosphoryl azide (DPPA) can be applied.

The Yamada-Curtius degradation usually takes place in the presence of a tertiary amine preferably triethylamine and in an inert solvent such as e.g. methylene chloride or ethylacetate.
Step d)
Step d) covers the transformation of the oxazolidinone of formula (V) into a cyclohexenol
of formula (VI). "
This transformation comprises the introduction of an amino protecting group R^ and a subsequent base induced transformation to the cyclohexenol of formula (VI).
Suitable substituents of the amino group R are as stated above, however , the BOC group is the preferred group.
Introduction of the amino protecting group is known to the skilled in the art.
Suitable base for the subsequent base induced transformation is an alkalihydride, an alkalialcoholate, diazabicyclo undecen (DBU) or a tetraalkyl guanidine. Preferred base is sodium hydride applied in amounts of 0.5 to 25 mol%.
Usually the reaction takes place in an inert solvent such as methylene chloride , toluene, tetrahydrofurane, ethylacetate at reflux temperature of the respective solvent.
The cyclohexenol of formula (VI) can be isolated from the reaction mixture by methods known to the skilled in the art.
Step e)

Step e) comprises the formation of an azide of formula (VII).
This step involves in a first sequence the transformation of the hydroxy group into a suitable leaving group and in a second sequence the azide formation, thereby leading to an inversion of configuration at the reaction centre.
The transformation of the OH group into a leaving group can be performed by sulfonylation i.e. converting the OH group into a sulfonic acid ester.
Agents commonly used for producing such sulfonic esters are e.g. the halogenides orfthe anhydrides of the following sulfonic acids: methane sulfonic acid, p-toluenesulfonic acid a p-nitrobenzenesulfonic acid, p-bromobenzenesulfonic acid or trifluoromethanesulfonic acid.
Preferred agent is a halogenide or anhydride of trifluoro methane sulfonic acid such as trifluoro methane sulfonic anhydride.
The sulfonylating agent is expediently added in an amount of 1.0 to 1.5 equivalents relating to one equivalent of the cyclohexenol of formula VI in presence of about two equivalents of a suitable base.
The reaction usually takes place in an inert solvent such as in methylene chloride and at reaction temperatures between -20°C and room temperature.
The sulfonic acid ester formed can be isolated and purified, e.g. by crystallization or directly be introduced into the following reaction sequence.
Azide formation is effected by treating the sulfonic acid ester intermediate previously obtained with a suitable azide whereby inversion of the configuration takes place. Azides commonly used are alkaliazides like sodium azide in amounts of 1 to 2 equivalents. The reaction takes place in a solvent such as in dimethyl sulfoxide, N,N-dimethylformamide, ethanol or acetone at temperatures betwen -10°C and 50°C.
Stepf)

Step f) covers the reduction of the azide and the subsequent acylation of the resuhing amine to form the respective acylated amine of the formula (VIII).
Reduction takes place either by a) a classical metal catalysed hydrogenation with hydrogen or b) by reduction of the azide with a phosphine.
According to method a) common hydrogenation catalysts such as e.g. Pd, Pt, Raney-Ni or Raney-Co catalysts which may be applied on an inert support can be used.
The hydrogenation can take place in a suitable organic solvent e.g. in ethylacetate at temperatures between 20°C and 60°C at at hydrogen pressures between 1 and 50 bar.
Phosphines which according to method b) can suitably be used are trioctyl phosphine, triisobutyl phosphine and tri-n-butyl phosphine. Most preferred phosphine is the tri-n-butyl phosphine.
Typically the reduction is performed in a polar solvent such as in ethylacetate or in tetrahydrofurane in presence of 1 to 20 equivalents of water.
The reaction temperature, depending on the phosphine used, as a rule is chosen in the range of-20°C and 50°C.
The amine formed can be isolated but is preferably directly acylated in the following reaction sequence.
Acylation can be effected using acylating agents in the presence of a base and at conditions known to the skilled in the art. Suitable acylating agents as a rule are aliphatic or aromatic carboxylic acid halides or anhydrides. Preferred acylating agents are the common acetylating agents such as acetyl chloride or acetanhydride.
Step g)
Step g) comprises the removal of the amino protecting group R* and if necessary the formation of the respective pharmaceutically acceptable salt of the 4,5-diamino shikimic acid derivative of formula (I).

The amino protecting group R* can be removed following methods well known to the skilled in the art. The preferred BOC group can e.g. easily be splitted off with HBr in acetic acid at room temperature or with HCl in ethylacetate.
The free amine can then be liberated with e.g. an aqueous base and then further be transformed into the pharmaceutically acceptable addition salt following the methods described in J.C.Rohloff et al., J.Org.Chem. 63, 1998, 4545-4550; WO 98/07685).
The term "pharmaceutically acceptable acid addition salts" embraces salts with inorganic and organic acids, such as hydrochloric acid, hydrobromic acid, nitric acid, sulfuric acid, phosphoric acid, citric acid, formic acid, fumaric acid, maleic acid, acetic acid, succinic acid, tartaric acid, methane sulfonic acid, p-toluenesulfonic acid and the like.
The salt formation is effected at room temperature in accordance with methods which are known per se and which are familiar to any person skilled in the art.
The preferred pharmaceutically acceptable acid addition salt is the 1:1 salt with phosphoric acid which can be formed preferably in ethanolic solution at a temperature of-20°C to 50°C.
The invention further comprises a process for the the preparation of an isophtalic acid derivative of the formula

wherein R", R^ and R^ are as above

which is characterized in that a dialkoxyphenol of the formula

wherein R^ is as above
is
in step aa)
converted into a trialkoxybenzene of the formula

wherein R and R are as above,
and in step ab)
further halogenated to a dihalotrialkoxy benzene of the formula


wherein R" and R^ are as above and X stands for a halogen atom and finally
in step ac)
carbonylated to form the product of the formula II.
step aa)
Etherification of the dialkyloxyphenol of formula X can be performed with the methane sulfonic acid ester of the respective alcohol R"OH. Reaction as a rule takes place in the presence of a strong base such as an alkah alcoholate in an inert solvent.
Alternatively etherification can happen under Mitsunobu conditions (O. Mitsunobu, Synthesis, 1981, 1) i.e. by treatment of the dialkoxyphenol of formula X with the respective alcohol R"OH in the presence of diisopropyl azodicarboxylate (DIAD) and triphenyl phosphine in a suitable inert solvent like tetrahydrofuran.
step ab)
The halogenation in this step preferably is a dibromination.
A suitable bromination agent for the trialkoxybenzene of formula XI is e.g. N-bromo succinimide (NBS).
Dibromination usually takes place with 2 equivalents NBS in a polar solvent such as in N,N-dimethylformamide at temperatures between -10°C and 50°C.

step ac)
Carbonylation of the dihalotrialkoxybenzene of formula XII can be performed with carbon monoxide in the presence of suitable catalyst in an alcoholic solvent like ethanol.
Suitable catalysts are metal complexes formed by a metal compound of the group VIII element of the periodoc table and a phosphine compound e.g. of palladium acetate and 1,3-bis (diphenyl phosphino) propane (dppp) or triphenylphosphine.
Usually the reaction is performed at temperatures of 80°C to 150°C and at CO-pressures up to 20 bar.
The invention further comprises a process for the preparation of an all-cis-cyclohexane dicarboxylate derivative of the formula

wherein R", R^ and R^ are as above
which is characterized in that an isophtalic acid derivative of the formula


wherein R\ R^ and R^ are as above
is hydrogenated.
This step is identical to step a) of the multistep synthesis described herein above. The repsective description of step a) is incorporated herein by reference.
The invention further comprises a selective hydrolysis and, if necessary, a dealkylation of an all-cis-cyclohexane dicarboxylate of the formula

wherein R\ R^ and R^ are as above,
to form the (S)- or (R)-cyclohexane monoacid of the formulas.

wherein R^ and R^ are as above.
This step is equivalent to step b) of the multistep synthesis described herein above. The respective description of step b) is incorporated herein by reference.

The following key intermediates are new and not known to the state of the art, they accordingly are an essential element of the present invention.

wherein R", R^ and R^ are as above, preferably 5-( l-ethyl-propoxy)-4,6-dimethoxy isophtalic acid ethyl ester with R" = 1-ethyl-propyl, R^ = ethyl and R^ = methyl.

wherein R", R^ and R^ are as above, preferably all-cis-5-(l-ethyl-propoxy)-4,6-dimethoxy-cyclohexane-l,3-dicarboxylic acid diethylester with R" = 1-ethyl propyl, R" = ethyl and R^ = methyl and all-cis-5-(l-ethyl-propoxy)-4,6-dihydroxy-cyclohexane-l,3-dicarboxylic acid diethylester with R" = 1-ethyl propyl, R^ = ethyl and R^ = H.


wherein R" and R^ are as above, preferably all-cis-(lR,3S,4S,5S,6R)-5-(l-ethyl
propoxy)-4,6-dihydroxy cyclohexane-l,3-dicarboxylic acid 1-ethyl ester with R = 1-
ethyl propyl, R^ = ethyl "

wherein R" and R^ are as above, preferably all-cis-(lS,3R,4R,5R,6S)-5-(l-ethyl propxy)-4,6-dihydroxy cyclohexane-l,3-dicarboxylic acid 1-ethyl ester with R = 1-ethyl propyl, R^ = ethyl.

wherein R^ and R^ are as above, preferably (3aS,5R,6R,7R,7aS)-7-( 1-ethyl propoxy)-6-hydroxy-2-oxo-octahydrobenzooxazole-5-carboxylic acid ethyl ester with R" = 1-ethyl propyl and R^ = ethyl and (3aR,5S,6S,7S,7aR)-7-( 1-ethyl propox\")-6-hydroxy-2-oxo-octahydrobenzooxazole-5-carboxylic acid ethyl ester with R" = 1-ethyl propyl and R^ = ethyl.


wherein R",R^ and R^ are as above, preferably (3R,4S,5S)-5-tert.-butoxy carbonyl-amino-3-(l-ethyl-propoxy)-4-hydroxy cyclohex-1-ene carboxylic acid ethyl ester (Via) with R" = 1-ethyl propyl, R^ = ethyl and R^ = tert.-butoxy carbonyl and (3S,4R,5R)-5-tert.-butoxy carbonyl-amino-3-(l-ethyl-propoxy)-4-hydroxy cyclohex-1-ene carboxylic acid ethyl ester (VIb) with R} = 1-ethyl propyl, R^ = ethyl and R^ = tert.-butoxy carbonyl.

wherein R", R^and R^ are as above, preferably (3R,4R,5S)-4-azido-5-tert.-butoxy carbonylamino-3-(l-ethyl propoxy) cyclohex-1-ene carboxylic acid ethyl ester (Vila) with R" = 1-ethyl propyl, R^ = ethyl and R^ = tert.-butoxy carbonyl and (3S,4S,5R)-4-azido-5-tert.-butoxy carbonylamino-3-(l-ethyl propoxy) cyclohex-1-ene carboxylic acid ethyl ester (Vllb) with R" = 1-ethyl propyl, R" = ethyl and R^ = tert.-butoxy carbonyl
The following examples shall illustrate the invention in more detail without limiting it.

Example 1
Preparation of methanesulfonic acid 1-ethyl-propyl ester
To a colorless solution of 88.15 g 3-pentanol (1.0 mol) in 150 ml pyridine were added under stirring at 0°C 126.0 g methanesulfonyl chloride (1.1 mol) over Ih. After warming up (15 min.) and stirring at room temperature for Ih , 50 ml deionized water were added all at once and stirring at room temperature was continued for Ih. The reaction mixture was diluted with 500 ml ethyl acetate and washed with 800 ml IN HCl and 250 ml 10% brine. Both aqueous layers were extracted sequentially with 250 ml ethyl acetate. After drying the combined organic layers over ca. 20 g Na2SO4, the solvent was removed on the rotary evaporator (50°C/> 1 mbar) affording 154.4 g (92.9%) yellow, oily title product, which could be used in the next step without purification.
Example 2 Preparation of (l-ethyl-propoxy)-l,3-dimethoxy-benzene
To a yellow solution of 38.5 g 2,6-dimethoxy phenol (0.25 mol) and 83.1 g methanesulfonic acid 1-ethyl-propyl ester (0.50 mol) in 500 ml dimethylsulfoxid was added under stirring at 50°C a solution of 56,1 g potassium tert.-butylate (0.50 mol) in 500 ml dimethylsulfoxid over 4h . After additional 2.8 g potassium tert.-butylate (0.025 mol) were added, stirring at 50°C was continued for Ih. The reaction mixture was distributed between 500 ml ethyl acetate and 600 ml IN HCl. The organic layer was washed twice with 250 ml, a total of 500 ml deionized water and the aqueous layers were extracted sequentially with 250 ml ethyl acetate. The combined organic layers were dried over ca. 25 Na2SO4, filtered and the solvent was evaporated by rotary evaporation (50°C/> 1 mbar) affording 56.2 g (100.2%) of the title product as an orange oil, which was used without purification in the next step (bp. 90°C/0.03 mbar).

Example 3 Preparation of l,5-dibromo-3-(l-ethyl-propoxy)-2,4-dimethoxy-benzene)
To a solution of 44.9 g crude (l-ethyl-propoxy)-l,3-dimethoxy-benzene (0.20 mol) in 60 ml N,N-dimethylformamide was added at 0°C a solution of 73.4 g N-bromosuccininfide (0.4 mol) in 160 ml N,N-dimethylformamide over 1 h. After warming to room temperature (0.5 h) and stirring at ambient temperature for 18 h, the red-brown reaction mixture was distributed between 400 ml ethyl acetate and 400 ml 5% brine. The organic layer was washed twice with 200 ml, a total of 400 ml 5% brine and all aqueous layers were extracted sequentially with 200 ml ethyl acetate. The combined organic layers were stirred with ca. 4 g charcoal for 1 h, filtered over ca. 20 g filter aid (Hyflo). Removal of the solvent by rotary evaporation (50°C/> 1 mbar) afforded 78.7 g (103%) crude title product which was dissolved in 400 ml 80% (v/v) ethanol-H20 at 50°C Crystallization by cooling down and stirring at 20°C for 18 h afforded after filtration and washing with ca. 40 ml -20° cold 80% (v/v) ethanol-H20 and drying (35°C/1 mbar/lSh) 69.0 g (90.3%) light yellow title product, mp. 47-48°C.
Example 4
Preparation of 5-(l-ethyl-propoxy)-4,6- dimethoxy-isophthalic acid diethyl ester
The autoclave was charged with 38.21 g l,5-dibromo-3-(l-ethyl-propoxy)-2,4-dimethoxy-benzene (0.10 mol), 39.26 g potassium acetate (0.40 mol), 200 ml ethanol, 0.11 g palladium(II)acetate (0.5 mmol) and 0.25 g l,3-bis(diphenylphosphino)propane (0.6 mmol). The autoclave was sealed, pressurized and vented four times with 10 bar of carbon monoxide with stirring (200 rpm) and finally the reaction mixture was heated to 110°C with stirring (600 rpm). The CO pressure was adjusted to 10 bar and the reaction was continued at constant pressure (10 bar at 110°C) for 15 h. After cooling down, the autoclave was vented and the reaction mixture poured to a stirred mixture of 100 ml

hexane and 200 ml 5% aqueous Na2C03. The aqueous layer was separated and extracted with 100 ml hexane. Both organic layers were washed sequentially with 100 ml IN HCl, combined and dried over ca. 10 g Na2SO4. After filtration and removal of the solvent by rotary evaporation (50°C/> 1 mbar) the resulting 35.7 g yellow, oily residue were distilled on the high vacuum, affording 34.9 g (94.6%) of the title product as a light yellow oil, bp. 140°C/0.02 mbar.
Example 5
Preparation of rt//-a"s-5-(l-ethyl-propoxy)-4,6-dimethoxy-cyclohexane-l,3-dicarboxyHc
acid diethyl ester
The autoclave was charged with 36.84 g 5-(l-ethyl-propoxy)-4,6- dimethoxy-isophthalic acid diethyl ester (0.10 mol), 36.84 g 5% RU/AI2O3 catalyst and 250 ml ethyl acetate. The autoclave was sealed and pressurized three times under stirring with 5 bar of H2. The reaction mixture was then stirred under a pressure of 100 bar H2 at 60°C for 24 h. After cooling to room temperature, the autoclave was vented and flushed with argon. The black suspension was filtered over ca. 50 g filter aid (Hyflo) and the autoclave as well as the filtercake were washed with ca. 200 ml ethyl acetate. The combined, colorless filtrate was evaporated by rotary evaporation (50°C/> 1 mbar) affording 35.1 g (93.7%) solid, which was dissolved in 530 ml hexane at 50°C. Crystallization by cooling down and stirring at -20°C for 6 h afforded, after filtration, washing with ca. 50 ml -20°C cold hexane and drying (50°C/1 mbar/16h) 30.8 g (82.2%) white crystalline tide product, mp. 108-109°C.
Example 6
Preparation of fl//-c/5-5-(l-ethyl-propoxy)-4,6-dihydroxy-cyclohexane-l,3-dicarboxylic
acid diethyl ester
To a suspension of 60.0 g sodium iodide (0.40 mol) in 200 ml acetonitrile were added 0.360 g deionised water (0.02 mol). After stirring at 40°C for 30 min. 50.6 ml trimethylchlorosilane (0.40 Mol = 43.5 g) were added all at once and stirring at 40°C was continued for 1 h. 37.4 g all-cis-5-(l-ethyl-propoxy)-4,6-dimethoxy-cyclohexane-l,3-

dicarboxylic acid diethyl ester (0.10 mol) were added to the white suspension all at once and stirring at 40° C was continued for 14 h. After cooling to room temperature, the orange suspension was distributed between 500 ml ethyl acetate and 250 ml deionised water while the two layers were decolorized by the addition of ca. 2.5 g sodium thiosulfate. The organic layer was washed twice with 100 ml, a total of 200 ml 10% brine and all three aqueous layers were extracted sequentially with 100 ml ethyl acetate. The combined organic layers were dried over ca. 25 g Na2SO4, filtered and the solvent was evaporated by rotary evaporation (50°C/> 10 mbar). The white, crystalline residue (34.9 g) was dissolved in 200 ml refluxing methylcyclohexane and crystallized by cooling down and stirring at -20°C for 16 h. Filtration and washing with ca. 20 ml -20°C cold methylcyclohexane afforded after drying (50°C/10 mbar/16h) 33.6 g (97.0%) white title product, mp. 115-116.5°C.
Example 7
Preparation of a//-cw-(lR,3S,4S,5S,6R)-5-(l-ethyl-propoxy)-4,6-dihydroxy-cyclohexane-l,3-dicarboxylic acid 1-ethyl ester
A suspension of 34.40 g all-cis-5-(l-ethyl-propoxy)-4,6-dihydroxy-cyclohexane-l,3-dicarboxylic acid diethyl ester (0.10 mol) in 390 ml 10 mM Tris-buffer pH 8.0 was heated to 35°C under vigorous stirring. 3.44 ml pig liver esterase ("technical grade" Roche Diagnostics) were added and the suspension kept at pH 8.0 and 35°C by the controlled addition (pH-stat) of 1.0 N sodium hydroxide solution under vigorous stirring. After a total consumption over 46 h of 103.3 ml 1.0 N NaOH (1.04 equivalents), the pH of the solution was adjusted to 2.0 with ca. 13 ml 25 % HCl. The reaction mixture was extracted three times with 330 ml dichloromethane and the combined organic layers were dried over ca. 100 g Na2SO4. After filtration and removal of the solvent by rotary evaporation (40°C/> 5 mbar) the residue was dried on the vacuum over night (0.03 mbar) affording 29.52 g (93.4 %) of the title product as a colorless gum, which was used without purification in the next step.
[a]D = + 7.2°(CHCl3;c = l)

Example 8
Preparation of (3aS,5R,6R,7R,7aS)-7-(l-ethyl-propoxy)-6-hydroxy-2-oxo-octahydro-benzooxazole-5-carboxylic acid ethyl ester
To a solution of 31.2 g all-cis-(lR,3S,4S,5S,6R)-5-(l-ethyl-propoxy)-4,6-dihydroxy-cyclohexane-l,3-dicarboxylic acid 1-ethyl ester (0.10 mol) in 200 ml dichloromethan"e were added 10.1 g triethylamine (0.10 mol) and 29.0 g diphenyl phosphoryl azide (0.10 mol). The clear reaction mixture was then stirred under reflux for 16 h. After cooling down it was distributed between 200 ml dichloromethane and 300 ml IM HCl. The organic layer was washed with 300 ml 5% NaHCOj and three times with 300 ml, 5% brine. The aqeous layers were extracted sequentially twice with 200 ml, dichloromethane. The combined organic layers were dried with ca. 50 g Na2SO4, filtered and the solvent was evaporated by rotary evaporation (35°C/> 10 mbar). The white, crystalline residue (34.6 g) was dissolved in 300 ml refluxing butyl acetate and crystallized by cooling down an stirring at -20°C for 16 h. Filtration and washing with ca. 40 ml -20°C cold butyl acetate afforded after drying (50°C/10 mbar/16h) 25.4 g (80.5% over two steps) white, crystalline title product, mp. 180-181°C.
[a]D = + 31.2°(CHCl3;c = l)
Example 9
Preparation of (3R,4S,5S)-5-tert.-butoxycarbonylamino-3-(l-ethyl-propoxy)-4-hydroxy-
cyclohex-1-ene carboxylic acid ethyl ester
To 2.40 g di-tert.-butyl dicarbonate (11 mmol), 25 mg 4-dimethylaminopyridine (0.2 mmol) and 3.15 g (3aS,5R,6R,7R,7aS)-7-(l-ethyl-propoxy)-6-hydroxy-2-oxo-octahydro-benzooxazole-5-carboxylic acid ethyl ester (10 mmol) were added 50 ml toluene and the suspension was stirred at room temperature for 4 h. The solvent was removed by rotary evaporation (50°C/10 mbar) and the gummy residue was redissolved in 50 ml toluene.

After the addition of 1.15 g tetramethylguanidine (10 mmol) the reaction mixture was refluxed for 20 h, cooled to room temperature and washed with 20 ml 2N HCl and twice with 20 ml, a total of 40ml 10% brine. The aqueous layers were extracted sequentially with 25 ml toluene, the organic layers were combined and dried over Na2SO4. Filtration and rotary evaporation (50°C/10 mbar) gave 3.80 g crystalline residue, which was dissolved in 70 ml hot hexane (60°C) and crystallized by cooling down and stirring over night at -20°C. Filtration and washing with ca. 10 ml -20°C cold hexane afforded after drying (50°C/10 mbar/16h) 2.88 g (77.6%) white, crystalline title product, mp. 102-102.5°C.
[aJD = -52.5° (CHCb; c = 1)
Example 10a
Preparation of (3R,4S,5S)-5-tert.-butoxycarbonylamino-3-(l-ethyl-propoxy)-4-trifluoromethanesulfonyloxy-cyclohex-1-enecarboxylic acid ethyl ester
A solution of 3.71 g (3R,4S,5S)-5-tert.-butoxycarbonylamino-3-(l-ethyl-propoxy)-4-hydroxy-cyclohex-1-ene carboxylic acid ethyl ester) (10 mmol) and 1.61 ml pyridine (20 mmol) in 20 ml CH2CI2 was cooled to 0°C. 1.73 ml trifluoromethanesulfonic anhydride (10.5 mmol) were added over 10 min. and stirring at 0°C was continued for 1 h. The reaction mixture was washed with 10 ml IN HCl and twice with 10 ml, a total of 20 ml 10% brine. The aqueous layers were extracted sequentially with 10 ml methylene chloride and the combined organic layers were dried over Na2SO4. Filtration and rotary evaporation (30°C/10 mbar) gave 4.96 g (98.4%) beige, cristalHne title product, which was used without ftirther purifcation in the next step.

Example 10b
Preparation of (3R,4S,5S)-5-tert.-butoxycarbonylamino-3-(l-ethyl-propoxy)-4-trifluoromethanesulfonyloxy-cyclohex-1-enecarboxylic acid ethyl ester
To 4.80 g di-tert.-butyl dicarbonate (22 mmol), 49 mg 4-dimethylaminopyridine (0.4 mmol) and 6.31 g (3aS,5R,6R,7R,7aS)-7-(l-ethyl-propoxy)-6-hydroxy-2-oxo-octahydro-benzooxazole-5-carboxylic acid ethyl ester (20 mmol) were added 100 ml toluene and the suspension was stirred at room temperature for 4 h. After the addition of 20 mg 60% sodium hydride dispersion in oil (ca. 0.5 mmol), the reaction mixture was refluxed for 1 h, cooled to room temperature and the solvent was removed by rotary evaporation. The yellowish, semicrystalline crude (3R,4S,5S)-5-tert.-butoxycarbonylamino-3-(l-ethyl-propoxy)-4-hydroxy-cyclohex-l-ene carboxylic acid ethyl ester (7.83 g) was redissolved in 100 ml CH2CI2 and 3.22 ml pyridine (40 mmol) were added under stirring. After cooling to -10°C, 3.47 ml trifluoromethanesulfonic anhydride (21 mmol) were added by a syrringe over 10 min and stirring at -10°C was continued for 1 h. 20 ml IN HCl were added to the -10°C cold reaction mixture under stirring and the organic layer was washed twice with 20 ml, a total of 40 ml 10% brine. All aqueous layers were extracted sequentially with 20 ml CH2CI2 and the combined organic layers were dried over Na2SO4, filtered and the solvent was removed by rotary evaporation (30°/>10 mbar). The yellow, crystalline residue (10.0 g) was dissolved in 150 ml hot diisopropyl ether (68°C) and transferred into a new flask. After cooling to room temperature the suspension was stirred over night at -20°C. Filtration and washing with ca. 40 ml -20°C cold diisopropyl ether afforded after drying (50°C/10 mbar/16h) 8,35 g (82.9%) white, crystalline title product, mp. 122-123°C.
[a]D = -79.1°(CHCl3;c=l)
Example 11
Preparation of (3R,4R,5S)-4-azido-5-tert.-butoxycarbonylamino-3-(l-ethyl-propoxy)-
cyclohex-1-enecarboxylic acid ethyl ester

To a stirred suspension of 10.07 g (3R,4S,5S)-5-tert.-butoxycarbonylamino-3-(l-ethyl-propoxy)-4-trifluoromethanesulfonyloxy-cydohex-l-enecarboxylic acid ethyl ester (20 mmol) and 50 ml 90% aqueous acetone were added 1.43 g sodium azide (22 mmol) and the reaction mixture was stirred at room temperature for 15 h. The acetone was removed by rotary evaporation (40°C/>10 mbar) and the oily residue was distributed between 50 ml ethyl acetate and 25 ml 5% brine. The aqueous layer was extracted with 25 ml ethyl acetate and both organic layers were washed sequentially with 25 ml 5% brine. The combined organic layers were dried (Na2SO4) and the solvent was removed by rotary evaporation (40°C/>10 mbar) affording 8.00 g light yellow, oily residue, which was dissolved in 80 ml hot hexane (50-60°C), filtered and crystallized by cooling down and stirring at -20°C over night. Filtration and washing with ca. 20 ml -20°C cold hexane afforded after drying " (50710 mbar/16h) 6.15 g (77.6%) white, crystalline title product, mp. 92-93°C.
[a]D = -63.3°(CHCl3;c=l)
Example 12
Preparation of (3R,4R,5S)-4-acetylamino-5-tert.-butoxycarbonylamino-3-( 1-ethyl-propoxy)-cyclohex-l-ene carboxylic acid ethyl ester
A solution of 1.59 g (3R,4R,5S)-4-azido-5-tert.-butoxycarbonylamino-3-(l-ethyl-propoxy)-cyclohex-l-enecarboxylic acid ethyl ester (4 mmol) and 0.36 ml water (20 mmol) in 5 ml tetrahydrofurane was cooled to 0°C. 1.12 ml triethylamine (8 mmol) and 0.38 ml acetic anhydride were added and stirring at 0°C was continued for 15 min.1.14 ml tri-n-butyl phosphine (4.4 mmol) were added over 5 min. and the yellowish solution was stirred for 30 min. at 0°C and then for 1 h at room temperature. After the addition of 5.58 ml triethylamine (40 mmol) 1.89 ml acetic anhydride (20 mmol) were added slowely under ice cooling and stirring at room temperature was continued for 1 h. The reaction mixture was diluted with 30ml ethyl acetate and washed sequentially with 25 ml 2N HCl, 10 ml 10% Na2C03 and 20 ml 10% brine. The aqueous layers were extracted sequentially with 20 ml ethyl acetate. The combined organic layers were dried (Na2SO4) and the solvent was removed by rotary evaporation (30°C/>10 mbar) affording 2.89 g crude, which was purified by chromatography on Si02 (100 g) with hexane ethyl acetate 1.4 : 1 (100 ml

fractions). Rotary evaporation (30°C/>10 mbar) gave 1.39 g (84%) of the title product as a colorless, crystalline residue, mp. 153.5-154.5°C.
[a]D = -89.7° (CHCI3; c = 1)
Example 13a
Preparation of (3R,4R,5S)-4-acetylamino-5-amino-3-(l-ethyl-propoxy)-cyclohex-l-enecarboxylic acid ethyl ester phosphoric acid salt
To a solution of 10.31 g (3R,4R,5S)-4-acetylamino-5-tert.-butoxycarbonylamino-3-(l-ethyl-propoxy)-cyclohex-l-enecarboxylic acid ethyl ester (25 mmol) in 100ml ethyl acetate were added at room temperature. 25 ml 5N HCl in ethyl acetate. After 20 min. a white precipitate was formed and the thick suspension was stirred at room temperature for 24 h. The suspension was diluted with 125 ml ethyl acetate, washed with ca. 40 ml 3N NaOH (pH ca. 9.5) and 50 ml 10% brine. The aqueous layers were extracted sequentially twice with 125 ml, a total of 250 ml ethyl acetate. The combined organic layers were dried (Na2SO4) and the solvent was removed by rotary evaporation (30°C/>10 mbar) affording 8.06 g (3R,4R,5S)-4-acetylamino-5-amino-3-(l-ethyl-propoxy)-cyclohex-l-enecarboxylic acid ethyl ester which was dissolved in 50 ml ethanol and added over ca. 2h to a warm solution (55°C) of 2.45 g 99% phosphoric acid (25 mmol) in 50 ml ethanol. (After the addition of ca. 2/3 of (3R,4R,5S)-4-acetylamino-5-amino-3-(l-ethyl-propoxy)-cyclohex-l-enecarboxylic acid ethyl ester, the clear solution was seeded with pure title product). After cooling down and stirring at 0-5°C for 3 h, the suspension was filtered, washed twice with 40 ml, a total of 80 ml acetone and dried (50°C/10 mbar/16h) affording 9,07 g (88.4%) white, crystalline title product, mp. 201-202°C.
[a]D = -32.1°(H20;c=l)

Example 13b
Preparation of (3R,4R,5S)-4-acetylamino-5-amino-3-(l-ethyl-propoxy)-cyclohex-l-enecarboxylic acid ethyl ester phosphoric acid salt
To a solution of 3.96 g (3R,4R,5S)-4-azido-5-tert.-butoxycarbonylamino-3-(l-ethylpropoxy)cyclohex-l-enecarboxylic acid ethylester (10 mmol) in 50 ml ethyl acetate were added 2.0 g wet Raney-Cobalt catalyst and the suspension was stirred and hydrogenated at room temperature for 20 h (-1.1 bar H2; 500 rpm). After removing the catalyst by filtration, 1.53 ml triethylamine (11 mmol =1.11 g) and 0.99 ml acetic , anhydride (10.5 mmol = 1.07 g) were added all at once and the colorless solution was stirred at room temperature for 1 h.Then 5.26 ml 5.7 M HBr/acetic acid (30 mmol HBr) were added to the colorless solution and the reaction mixture was stirred at room temperature for 20 h. Then ca. 55 ml 2 N NaOH (pH ca. 9.5) were added under stirring and the organic layer was separated and washed twice with 30 ml, a total of 60 ml 20% brine. All three aqueous layers were extracted sequentially and twice with 30 ml, a total of 60 ml ethyl acetate and the combined organic layers were dried (Na2SO4). After filtration and removal of the solvent by rotary evaporation (50°/> 1 mbar) the yellowish, viscous residue (3.47 g) was dissolved in 20 ml ethanol and added under stirring to a 50°C warm solution of 0.98 g ortho-phosphoric acid (10 mmol) in 40 ml ethanol over 30 min (after the addition of two third, the 50°C warm solution was seeded with pure title product). The white suspension was cooled down (2 h) and stirred at 0°C for 3 h. The crystals were filtered, washed with ca. 20 ml acetone and dried (50710 mbar/16h) affording 3.41 g (83.2%) white, crystalline phosphoric acid salt, mp. 198-199°C (dec).
[a]D = -32.1°(H20;c=l)
Example 14
Preparation of rt//-d5-(lS,3R,4R,5R,6S)-5-(l-ethyl-propoxy)-4,6-dimethoxy-cyclohexane-l,3-dicarboxylic acid 1-ethyl ester)
To a suspension of 74.9 g all-cis-5-(l-ethyl-propoxy)-4,6-dimethoxy-cyclohexane-l,3-dicarboxylic acid diethyl ester (0.20 mol) in 240 ml cyclohexane was added 1.11 0.1 M glucose in water and 60 ml 0.1 M sodium phosphate buffer pH 7.0, and the mixture was heated to 35°C under vigorous stirring. 560 mg Lipase from Aspergillus oryzae (Fluka

62285) was added and the emulsion/suspension kept at pH 7.0 and 35°C by the controlled addition (pH-stat) of 1.0 N sodium hydroxide solution under vigorous stirring. After a total consumption of 187.5 ml 1.0 N sodium hydroxide (0.94 equivalents) after 20 h the pH was set to 2.0 with ca. 200 ml 1 N hydrochloric acid and the reaction mixture extracted with 1.5 1 dichloromethane. The whole emulsion was filtered through a bed of 150 g dicalite filter aid and the aqueous phase extracted again with 2x1.5 1 dichloromethane which were passed through the dicalite bed before use. The combined organic phases were dried on 175 g Na2SO4, filtered, concentrated (13mbar/50°C/lh) and the residue dried overnight on a high vacuum to give 69.42 g (100%) white crystalline title product, mp. 147-148°C.
[a]D = +7.4°(CHCl3;c=l)
Example 15
Preparation of all-cis-(lS,3R,4R,5R,6S)-5-(l-ethyl-propoxy)-4,6-dihydroxy-cycIohexane-l,3-dicarboxylic acid 1-ethyl ester)
To a stirred suspension of 30.0 g sodium iodide (0.20 mol) in 100 ml acetonitrile were added 21.7 g trimethyl-chlorsilane (0.20 mol; 25.3 ml) all at once. After stirring at room temperature for 0.5 h 17.3 g all-cis-5-(l-ethyl-propoxy)-4,6-dimethoxy-cyclohexane-l,3-dicarboxylic acid 1-ethyl ester (0.050 mol) were added and stirring at room temperature was continued for 12 h. The reaction mixture was distributed between 250 ml dichloromethane and 250 ml deionized water. After the two reddish phases were decolorized by the addition of ca. 0.25 g Na2S2O3, the organic layer was washed twice with 100 ml, a total of 200 ml 10% brine. All aqueous layers were then extracted sequentially with 100 ml dichloromethane. The combined organic layers were dried over Na2SO4, filtered and the solvent was evaporated by rotary evaporation (50°C/> 1 mbar) affording 15.8 g (99.4%) of the title product as a colorless gum, which was used without purification in the next step.
[a]D = -7.2o(CHCl3;c=l)

Example 16
Preparation of all-cis-(lS,3R>4R,5R,6S)-7-(l-ethyl-propoxy)-6-hydroxy-2-oxo-octahydro-
benzooxazole-5-carboxylic acid ethyl ester
To a solution of 15.77 g all-cis-(lS,3R,4R,5R,6S)-5-(l-ethyl-propoxy)-4,6-dihydroxy-cyclohexane-l,3-dicarboxylic acid 1-ethyl ester (50 mmol) in 100 ml dichloromethane were added 5.06 g triethylamine (50 mmol) and 14.48 g diphenyl phosphoryl azide (50 mmol). The clear reaction mixture was then stirred under reflux for 16 h. After cooling down it was distributed between 100 ml dichloromethane and 150 ml IM HCl. The organic layer was washed with 150 ml 5% NaHCO3 and three times with 150 ml, a total of 450 ml 5% brine. All five aqeous layers were extracted sequentially twice with 100 ml,"a total of 200 ml dichloromethane. The combined organic layers were dried with ca. 25 g Na2SO4, filtered and the solvent was evaporated by rotary evaporation (35°C/> 10 mbar). The white, crystalline residue (17.4 g) was dissolved in 150 ml refluxing butyl acetate and crystallized by cooling down and stirring at -20°C for 16 h. Filtration and washing with ca. 20 ml -20°C cold butyl acetate afforded after drying (50°C/10 mbar/16h) 12.6 g (79.9% over three steps) white, crystalUne title product, mp. 180.5-181°C.
[a]D = -31.1°(CHCl3;c=l)





The present invention relates to a multi step process for the preparation of 4,5-diamino shikimic acid derivatives, especially for the preparation of (3R,4R,5S)-4-acetamido-5-amino-3-(l-ethylpropoxy)-l-cyclohexene-l-carboxylic acid ethylester and its pharmaceutically acceptable addition salts starting from isophthalic acid derivatives," individual process steps thereof, as well as new specific intermediates.
4,5-diamino shikimic acid derivatives, especially the (3R,4R,5S)-4-acetamido-5-amino-3-(l-ethylpropoxy)-l-cyclohexene-l-carboxylic acid ethylester and its pharmaceutically acceptable addition salts are potent inhibitors of viral neuraminidase ( J.C.Rohloff et al., J.Org.Chem., 1998, 63, 4545-4550; WO 98/07685).
A multi step synthesis of (3R,4R,5S)-4-acetamido-5-amino-3-(l-ethylpropoxy)-l-cyclohexene-1-carboxylic acid ethylester from (-)-quinic acid or (-)-shikimic acid is described in (J.C.Rohloff et al, loc.cit.).
Both (-)-quinic acid and (-)-shikimic acid are starting compounds which are rather expensive and hardly accessible in technical quantities. A multi step synthesis capable to run on a technical scale should therefore preferably be based on starting compounds which are more attractive in price and available in technical quantities.
Object of the present invention therefore is to provide such a new access to the 4,5-diamino shikimic acid derivatives mentioned above in good yields and excellent quality.

It was found that with the synthesis according to claim 1 this object could surprisingly be achieved.
/The present invention therefore relates to a process for the preparation of a 4,5-diamino shikimic acid derivative of formula

and pharmaceutically acceptable addition salts thereof
wherein R1 is an optionally substituted alkyl group,
R2 is an alkyl group and
R3 and R4, independent of each other are H or a substituent of an amino group, with
the proviso that both R3 and R4 are not H
and which is characterized in that in step a)
an isophtalic acid derivative of the formula


wherein R1 and R2 are as above and R5 is H or lower alkyl is hydrogenated to form an all-cis-cyclohexane dicarboxylate of the formula

wherein R", R and R are as above,
in step b)
the cyclohexane dicarboxylate of formula (III) is, if R5=H, selectively hydrolyzed to form the (S)- or (R)-cyclohexane monoacid of formulas IVa or IVb or, if R5=lower alkyl, either dealkylated first and then selectively hydrolyzed or selectively hydrolyzed first and then dealkylated to form the (S)- or (R)-cyclohexane mono acid of the formulas


wherein R and R are as above, in step c)
the cyclohexane monoacid of the formula (IVa) is further converted to an oxazohdinone of the formula

wherein R and R are as above,
in step d)
the oxazohdinone of formula (V) is transformed into a cyclohexenol of the formula

wherein R1 and R2 are as above and R6 is an amino protecting group

in step e)
the cyclohexenol of formula (VI) is further converted into an azide of formula

wherein R", R and R^ are as above,
in step f)
the azide of formula (VII) is reduced and acylated to form the acylated amine of the formula


wherein R1 R2 R3 R4 and R5 are as above, and in step g)
the acylated amine of the formula (VIII) is finally transferred into the 4,5-diamino shikimic acid derivative of formula (I) by removing the amino protecting group R and if necessary by forming the respective pharmaceutically acceptable salt.
The term alkyl in R" has the meaning of a straight chained or branched alkyl group of 1 to 20 C-atoms, expediently of 1 to 12 C-atoms. Examples of such alkyl groups are methyl, ethyl, n-propyl, i-propyl, n-butyl, i-butyl, tert.-butyl, pentyl and its isomers, hexyl and its isomers, heptyl and its isomers, octyl and its isomers, nonyl and its isomers, decyl and its isomers, undecyl and its isomers and dodecyl and its isomers.
This alkyl group can be substituted with one or more substituents as defined in e.g. WO 98/07685. Suitable substituents are alkyl of 1 to 6 C-atoms (as defined above), alkenyl of 2 to 6 C-atoms, cycloalkyl with 3 to 6 C-atoms, hydroxy, alkoxy with 1 to 6 C-atoms, alkoxycarbonyl with 1 to 6 C-atoms, F, CI, Br, and J. Preferred meaning for R"is 1-ethylpropyl.
R is a straight chained or branched alkyl group of 1 to 12 C-atoms, expediently of 1 to 6 C-atoms as exemplified above.
Preferred meaning for R is ethyl.
R5 is a lower n-alkyl group of 1 to 3 C-atoms, preferably methyl.
R3 and R4 is a substituent of an amino group conventionally used and known in the art and described e.g. in WO 98/07685.
R3 and R4 preferably stand for alkanoyl groups, more preferably lower alkanoyl with 1 to 6 C-atoms such as hexanoyl, pentanoyl, butanoyl (butyryl), propanoyl (propionyl), ethanoyl (acetyl) and methanoyl (formyl). Preferred alkanoyl group and therefore preferred meaning for R3 is acetyl and for R4" is H.

R^ is a common amino protecting group conventionally used and known in the art and described e.g. in "Protective Groups in Organic Chemistry", Theodora W. Greene et al., John Wiley & Sons Inc., New York, 1991, 315-385.
R^ suitably is benzyloxycarbonyl (Z), tert.-butyloxycarbonyl (BOG), allyloxycarbonyl (Alloc) or 9-fluorenylmethoxycarbonyl (FMOC), preferably tert.-butoxycarbonyl (BOG).
Preferred 4,5-diamino shikimic acid derivative of formula (I) is the (3R,4R,5S)-4-acetamido-5-amino-3-(l-ethylpropoxy)-l-cyclohexene-l-carboxyIic acid ethylester and the (3R,4R,5S)-4-acetamido-5-amino-3-(l-ethylpropoxy)-l-cyclohexene-l-carboxyric acid ethyl ester phosphate (1:1).
Provided that the process from step c) onwards is run with the cyclohexane monoacid of the formula (IVb) the process of the present invention allows to produce the (+)-enantiomer of the 4,5-dimino shikimic acid derivative having the formula

wherein R^ R^ R^ and R^ are as above and all the (+)-enantiomers of the corresponding intermediates.
Step a)
Step a) comprises the hydrogenation of an isophtalic acid derivative of the formula (II) to an all-cis- cyclohexane dicarboxylate of the formula (III).

Hydrogenation takes place with hydrogen in the presence of a common hydrogenation catalyst which may be applied on an inert support. Suitable hydrogenation catalysts are rhodium or ruthenium applied in an amount of 1 to 10% on an inert support, such as on aluminium oxide or charcoal.
The hydrogenation can be effected in an inert solvent like ethylacetate, ethanol, tetrahydrofuran or tert.-butyl methyl ether at temperatures between 20°C and 150°C and at hydrogen pressures between 1 bar and 200 bar .
The resulting cydohexane dicarboxylate of the formula (III) shows an all-cis meso form and therefore is optically inactive.
Step b)
Step b) comprises a selective enzymatic hydrolysis and, if necessary, a dealkylation of the cydohexane dicarboxylate of the formula (III) to either the (S)- or (R)-cydohexane mono acid of the formulas (IVa) or (IVb).
Starting from the cydohexane dicarboxylate of formula (III) with R =H selective enzymatic hydrolysis can directly take place, however, starting from the cydohexane dicarboxylate of formula (III) with R^=lower alkyl dealkylation can either take place before or after the selective hydrolysis.
The dealkylation, can take place with an alkali iodide in the presence of a trialkylhalogen silane. Dealkylation preferably is a demethylation and preferably sodium iodide together with trimethylchlorosilane is used.
This dealkylation as a rule is performed in an inert solvent, such as in acetonitril at temperatures between 20°C and 80 °C.

Selective hydrolysis comprises an enzymatic hydrolysis of the cyclohexane dicarboxylate of the formula (III), whereby the choice of the enzyme determines whether the (S)-monoacid of the formula

or the (R)-monoacid isomer of the formula

can be obtained.
In order to achieve the 4,5-diamino shikimic acid of formula (la) with the desired stereo configuration the subsequent reaction steps have to be performed with the (S)-monoacid of formula (IVa).
Starting with the all-cis-cyclohexane dicarboxylate of formula III with R = H suitable enzymes to gain the (S)-isomer of formula (IVa) are esterases of the EC class 3.1.1.1, preferably mammalian esterases (e.g. from pig, bovine or horse). The most preferred

enzyme is pig liver esterase (which is subsequently termed PLE). Commercial preparations ofPLE can be purchased e.g. from Roche Diagnostics, Fluka, Sigma, Amano or Altus. Also less purified PLE preparations (e.g. "PLE technical grade" from Roche Diagnostics) or only poorly purified preparations (e.g. such as "pig liver acetone powder" from Fluka) can be used as well as PLE preparations with enriched or separated isozyme fractions (like e.g. Chirazyme E-1 or Chirazyme E-2 from Roche Diagnostics).
As a common alternative the enzymes may be used in immobilized form.
The substrate is applied as a suspension in an aqueous solution in a 5 - 15% concentration (w/w), preferably around 10%. A suitable reaction temperature is room temperature to 35°C, a suitable reaction pH between 6.5 and 8.5.
As to the aqueous phase, common buffer solutions known to be used for biochemical conversions are used like e.g. phosphate or Tris-buffer in a concentration of 5 - 50 mM. Such a buffer solution can additionally contain a salt like e.g. NaCl or KCl in a concentration of 50 to 300 mM. A preferred buffering system could e.g. contain 0.1 M KCl and 10 mM Tris-hydrochloride pH 8.0.
After addition of the enzyme the pH of the reaction mixture is maintained under stirring at the selected value by the controlled addition of a base such as NaOH or KOH, whereby the formed monoacid goes into solution and the reaction mixture becomes rather clear.
After termination of the reaction, the product is worked up conventionally by acidification of the reaction mixture and extraction with a common organic solvent.
Starting with the all-cis cyclohexane dicarboxylate of formula 111 with R = H or lower alkyl, preferably methyl, suitable enzymes to gain the (R)-isomer of formula (IVb) are lipases of the EC class 3.1.1.3. Suitable representatives of this class are the lipases from Aspergillus oryzae (commercially available at Fluka), Thermomyces lanuginosa (formerly termed Humicola lanuginosa; e.g. from Novo Nordisk) and from Mucor miehei (e.g. from Novo Nordisk). Again, also less purified crude enzyme preparations maybe used.
Again, as a common alternative, the enzymes may be used in immobilized form.
The reaction is carried out in an aqueous or an aqueous-organic biphasic system. Preferred is a biphasic system with a water-immiscible apolar solvent as co-solvent. Suitable co-solvents are alkanes or cycloalkanes, preferred is cyclohexane.

The substrate is applied (as a suspension) in the mono- or biphasic system in 5 - 10 % overall concentration (w/w). A suitable reaction temperature is room temperature to 35°C, a suitable reaction pH between 6.5 and 8.5.
As to the aqueous phase, common buffer solutions known to be used for biochemical conversions are used like e.g. phosphate, borate or Tris-buffer in a concentration of 5 - 50 mM. Such a buffer solution can additionally contain a salt like e.g. NaCl, KCl or a polyhydric alcohol such as a sugar (e.g. glucose) in a concentration of 50 to 300 mM. A preferred buffering system could e.g. contain 0.1 M glucose and 5 mM sodium phosphate pH 7.0.
The ratio organic solvent / aqueous phase is in the range of 1:10 to 1:1.
After addition of the enzyme the pH of the reaction mixture is maintained under stirring at the selected value by the controlled addition of a base such as NaOH or KOH.
After termination of the reaction, the product is worked up conventionally by acidification of the reaction mixture and extraction with a common organic solvent.
Step c)
Step c) comprises the conversion of the cyclohexane mono acid of the formula (IVa) into the oxazolidinone of formula (V).
This conversion can take place applying the known principles of a Curtius or of a Hoffmann degradation. Where in the Hofmann degradation the oxazolidinone is formed by transformation of the cyclohexane monoacid into the respective cyclohexane monoamide and by subsequent ring formation e.g. with a hyprochlorite, the Curtius degradation involves the formation of the cyclohexane azide intermediate.
As a suitable variation of the Curtius degradation a Yamada-Curtius degradation using dialkylphosphorylazides or diarylphosphoryl azides, preferably diarylphosphoryl azides, most preferably diphenyl phosphoryl azide (DPPA) can be applied.

The Yamada-Curtius degradation usually takes place in the presence of a tertiary amine preferably triethylamine and in an inert solvent such as e.g. methylene chloride or ethylacetate.
Step d)
Step d) covers the transformation of the oxazolidinone of formula (V) into a cyclohexenol
of formula (VI). "
This transformation comprises the introduction of an amino protecting group R^ and a subsequent base induced transformation to the cyclohexenol of formula (VI).
Suitable substituents of the amino group R are as stated above, however , the BOC group is the preferred group.
Introduction of the amino protecting group is known to the skilled in the art.
Suitable base for the subsequent base induced transformation is an alkalihydride, an alkalialcoholate, diazabicyclo undecen (DBU) or a tetraalkyl guanidine. Preferred base is sodium hydride applied in amounts of 0.5 to 25 mol%.
Usually the reaction takes place in an inert solvent such as methylene chloride , toluene, tetrahydrofurane, ethylacetate at reflux temperature of the respective solvent.
The cyclohexenol of formula (VI) can be isolated from the reaction mixture by methods known to the skilled in the art.
Step e)

Step e) comprises the formation of an azide of formula (VII).
This step involves in a first sequence the transformation of the hydroxy group into a suitable leaving group and in a second sequence the azide formation, thereby leading to an inversion of configuration at the reaction centre.
The transformation of the OH group into a leaving group can be performed by sulfonylation i.e. converting the OH group into a sulfonic acid ester.
Agents commonly used for producing such sulfonic esters are e.g. the halogenides orfthe anhydrides of the following sulfonic acids: methane sulfonic acid, p-toluenesulfonic acid a p-nitrobenzenesulfonic acid, p-bromobenzenesulfonic acid or trifluoromethanesulfonic acid.
Preferred agent is a halogenide or anhydride of trifluoro methane sulfonic acid such as trifluoro methane sulfonic anhydride.
The sulfonylating agent is expediently added in an amount of 1.0 to 1.5 equivalents relating to one equivalent of the cyclohexenol of formula VI in presence of about two equivalents of a suitable base.
The reaction usually takes place in an inert solvent such as in methylene chloride and at reaction temperatures between -20°C and room temperature.
The sulfonic acid ester formed can be isolated and purified, e.g. by crystallization or directly be introduced into the following reaction sequence.
Azide formation is effected by treating the sulfonic acid ester intermediate previously obtained with a suitable azide whereby inversion of the configuration takes place. Azides commonly used are alkaliazides like sodium azide in amounts of 1 to 2 equivalents. The reaction takes place in a solvent such as in dimethyl sulfoxide, N,N-dimethylformamide, ethanol or acetone at temperatures betwen -10°C and 50°C.
Stepf)

Step f) covers the reduction of the azide and the subsequent acylation of the resuhing amine to form the respective acylated amine of the formula (VIII).
Reduction takes place either by a) a classical metal catalysed hydrogenation with hydrogen or b) by reduction of the azide with a phosphine.
According to method a) common hydrogenation catalysts such as e.g. Pd, Pt, Raney-Ni or Raney-Co catalysts which may be applied on an inert support can be used.
The hydrogenation can take place in a suitable organic solvent e.g. in ethylacetate at temperatures between 20°C and 60°C at at hydrogen pressures between 1 and 50 bar.
Phosphines which according to method b) can suitably be used are trioctyl phosphine, triisobutyl phosphine and tri-n-butyl phosphine. Most preferred phosphine is the tri-n-butyl phosphine.
Typically the reduction is performed in a polar solvent such as in ethylacetate or in tetrahydrofurane in presence of 1 to 20 equivalents of water.
The reaction temperature, depending on the phosphine used, as a rule is chosen in the range of-20°C and 50°C.
The amine formed can be isolated but is preferably directly acylated in the following reaction sequence.
Acylation can be effected using acylating agents in the presence of a base and at conditions known to the skilled in the art. Suitable acylating agents as a rule are aliphatic or aromatic carboxylic acid halides or anhydrides. Preferred acylating agents are the common acetylating agents such as acetyl chloride or acetanhydride.
Step g)
Step g) comprises the removal of the amino protecting group R* and if necessary the formation of the respective pharmaceutically acceptable salt of the 4,5-diamino shikimic acid derivative of formula (I).

The amino protecting group R* can be removed following methods well known to the skilled in the art. The preferred BOC group can e.g. easily be splitted off with HBr in acetic acid at room temperature or with HCl in ethylacetate.
The free amine can then be liberated with e.g. an aqueous base and then further be transformed into the pharmaceutically acceptable addition salt following the methods described in J.C.Rohloff et al., J.Org.Chem. 63, 1998, 4545-4550; WO 98/07685).
The term "pharmaceutically acceptable acid addition salts" embraces salts with inorganic and organic acids, such as hydrochloric acid, hydrobromic acid, nitric acid, sulfuric acid, phosphoric acid, citric acid, formic acid, fumaric acid, maleic acid, acetic acid, succinic acid, tartaric acid, methane sulfonic acid, p-toluenesulfonic acid and the like.
The salt formation is effected at room temperature in accordance with methods which are known per se and which are familiar to any person skilled in the art.
The preferred pharmaceutically acceptable acid addition salt is the 1:1 salt with phosphoric acid which can be formed preferably in ethanolic solution at a temperature of-20°C to 50°C.
The invention further comprises a process for the the preparation of an isophtalic acid derivative of the formula

wherein R", R^ and R^ are as above

which is characterized in that a dialkoxyphenol of the formula

wherein R^ is as above
is
in step aa)
converted into a trialkoxybenzene of the formula

wherein R and R are as above,
and in step ab)
further halogenated to a dihalotrialkoxy benzene of the formula


wherein R" and R^ are as above and X stands for a halogen atom and finally
in step ac)
carbonylated to form the product of the formula II.
step aa)
Etherification of the dialkyloxyphenol of formula X can be performed with the methane sulfonic acid ester of the respective alcohol R"OH. Reaction as a rule takes place in the presence of a strong base such as an alkah alcoholate in an inert solvent.
Alternatively etherification can happen under Mitsunobu conditions (O. Mitsunobu, Synthesis, 1981, 1) i.e. by treatment of the dialkoxyphenol of formula X with the respective alcohol R"OH in the presence of diisopropyl azodicarboxylate (DIAD) and triphenyl phosphine in a suitable inert solvent like tetrahydrofuran.
step ab)
The halogenation in this step preferably is a dibromination.
A suitable bromination agent for the trialkoxybenzene of formula XI is e.g. N-bromo succinimide (NBS).
Dibromination usually takes place with 2 equivalents NBS in a polar solvent such as in N,N-dimethylformamide at temperatures between -10°C and 50°C.

step ac)
Carbonylation of the dihalotrialkoxybenzene of formula XII can be performed with carbon monoxide in the presence of suitable catalyst in an alcoholic solvent like ethanol.
Suitable catalysts are metal complexes formed by a metal compound of the group VIII element of the periodoc table and a phosphine compound e.g. of palladium acetate and 1,3-bis (diphenyl phosphino) propane (dppp) or triphenylphosphine.
Usually the reaction is performed at temperatures of 80°C to 150°C and at CO-pressures up to 20 bar.
The invention further comprises a process for the preparation of an all-cis-cyclohexane dicarboxylate derivative of the formula

wherein R", R^ and R^ are as above
which is characterized in that an isophtalic acid derivative of the formula


wherein R\ R^ and R^ are as above
is hydrogenated.
This step is identical to step a) of the multistep synthesis described herein above. The repsective description of step a) is incorporated herein by reference.
The invention further comprises a selective hydrolysis and, if necessary, a dealkylation of an all-cis-cyclohexane dicarboxylate of the formula

wherein R\ R^ and R^ are as above,
to form the (S)- or (R)-cyclohexane monoacid of the formulas.

wherein R^ and R^ are as above.
This step is equivalent to step b) of the multistep synthesis described herein above. The respective description of step b) is incorporated herein by reference.

The following key intermediates are new and not known to the state of the art, they accordingly are an essential element of the present invention.

wherein R", R^ and R^ are as above, preferably 5-( l-ethyl-propoxy)-4,6-dimethoxy isophtalic acid ethyl ester with R" = 1-ethyl-propyl, R^ = ethyl and R^ = methyl.

wherein R", R^ and R^ are as above, preferably all-cis-5-(l-ethyl-propoxy)-4,6-dimethoxy-cyclohexane-l,3-dicarboxylic acid diethylester with R" = 1-ethyl propyl, R" = ethyl and R^ = methyl and all-cis-5-(l-ethyl-propoxy)-4,6-dihydroxy-cyclohexane-l,3-dicarboxylic acid diethylester with R" = 1-ethyl propyl, R^ = ethyl and R^ = H.


wherein R" and R^ are as above, preferably all-cis-(lR,3S,4S,5S,6R)-5-(l-ethyl
propoxy)-4,6-dihydroxy cyclohexane-l,3-dicarboxylic acid 1-ethyl ester with R = 1-
ethyl propyl, R^ = ethyl "

wherein R" and R^ are as above, preferably all-cis-(lS,3R,4R,5R,6S)-5-(l-ethyl propxy)-4,6-dihydroxy cyclohexane-l,3-dicarboxylic acid 1-ethyl ester with R = 1-ethyl propyl, R^ = ethyl.

wherein R^ and R^ are as above, preferably (3aS,5R,6R,7R,7aS)-7-( 1-ethyl propoxy)-6-hydroxy-2-oxo-octahydrobenzooxazole-5-carboxylic acid ethyl ester with R" = 1-ethyl propyl and R^ = ethyl and (3aR,5S,6S,7S,7aR)-7-( 1-ethyl propox\")-6-hydroxy-2-oxo-octahydrobenzooxazole-5-carboxylic acid ethyl ester with R" = 1-ethyl propyl and R^ = ethyl.


wherein R",R^ and R^ are as above, preferably (3R,4S,5S)-5-tert.-butoxy carbonyl-amino-3-(l-ethyl-propoxy)-4-hydroxy cyclohex-1-ene carboxylic acid ethyl ester (Via) with R" = 1-ethyl propyl, R^ = ethyl and R^ = tert.-butoxy carbonyl and (3S,4R,5R)-5-tert.-butoxy carbonyl-amino-3-(l-ethyl-propoxy)-4-hydroxy cyclohex-1-ene carboxylic acid ethyl ester (VIb) with R} = 1-ethyl propyl, R^ = ethyl and R^ = tert.-butoxy carbonyl.

wherein R", R^and R^ are as above, preferably (3R,4R,5S)-4-azido-5-tert.-butoxy carbonylamino-3-(l-ethyl propoxy) cyclohex-1-ene carboxylic acid ethyl ester (Vila) with R" = 1-ethyl propyl, R^ = ethyl and R^ = tert.-butoxy carbonyl and (3S,4S,5R)-4-azido-5-tert.-butoxy carbonylamino-3-(l-ethyl propoxy) cyclohex-1-ene carboxylic acid ethyl ester (Vllb) with R" = 1-ethyl propyl, R" = ethyl and R^ = tert.-butoxy carbonyl
The following examples shall illustrate the invention in more detail without limiting it.

Example 1
Preparation of methanesulfonic acid 1-ethyl-propyl ester
To a colorless solution of 88.15 g 3-pentanol (1.0 mol) in 150 ml pyridine were added under stirring at 0°C 126.0 g methanesulfonyl chloride (1.1 mol) over Ih. After warming up (15 min.) and stirring at room temperature for Ih , 50 ml deionized water were added all at once and stirring at room temperature was continued for Ih. The reaction mixture was diluted with 500 ml ethyl acetate and washed with 800 ml IN HCl and 250 ml 10% brine. Both aqueous layers were extracted sequentially with 250 ml ethyl acetate. After drying the combined organic layers over ca. 20 g Na2SO4, the solvent was removed on the rotary evaporator (50°C/> 1 mbar) affording 154.4 g (92.9%) yellow, oily title product, which could be used in the next step without purification.
Example 2 Preparation of (l-ethyl-propoxy)-l,3-dimethoxy-benzene
To a yellow solution of 38.5 g 2,6-dimethoxy phenol (0.25 mol) and 83.1 g methanesulfonic acid 1-ethyl-propyl ester (0.50 mol) in 500 ml dimethylsulfoxid was added under stirring at 50°C a solution of 56,1 g potassium tert.-butylate (0.50 mol) in 500 ml dimethylsulfoxid over 4h . After additional 2.8 g potassium tert.-butylate (0.025 mol) were added, stirring at 50°C was continued for Ih. The reaction mixture was distributed between 500 ml ethyl acetate and 600 ml IN HCl. The organic layer was washed twice with 250 ml, a total of 500 ml deionized water and the aqueous layers were extracted sequentially with 250 ml ethyl acetate. The combined organic layers were dried over ca. 25 Na2SO4, filtered and the solvent was evaporated by rotary evaporation (50°C/> 1 mbar) affording 56.2 g (100.2%) of the title product as an orange oil, which was used without purification in the next step (bp. 90°C/0.03 mbar).

Example 3 Preparation of l,5-dibromo-3-(l-ethyl-propoxy)-2,4-dimethoxy-benzene)
To a solution of 44.9 g crude (l-ethyl-propoxy)-l,3-dimethoxy-benzene (0.20 mol) in 60 ml N,N-dimethylformamide was added at 0°C a solution of 73.4 g N-bromosuccininfide (0.4 mol) in 160 ml N,N-dimethylformamide over 1 h. After warming to room temperature (0.5 h) and stirring at ambient temperature for 18 h, the red-brown reaction mixture was distributed between 400 ml ethyl acetate and 400 ml 5% brine. The organic layer was washed twice with 200 ml, a total of 400 ml 5% brine and all aqueous layers were extracted sequentially with 200 ml ethyl acetate. The combined organic layers were stirred with ca. 4 g charcoal for 1 h, filtered over ca. 20 g filter aid (Hyflo). Removal of the solvent by rotary evaporation (50°C/> 1 mbar) afforded 78.7 g (103%) crude title product which was dissolved in 400 ml 80% (v/v) ethanol-H20 at 50°C Crystallization by cooling down and stirring at 20°C for 18 h afforded after filtration and washing with ca. 40 ml -20° cold 80% (v/v) ethanol-H20 and drying (35°C/1 mbar/lSh) 69.0 g (90.3%) light yellow title product, mp. 47-48°C.
Example 4
Preparation of 5-(l-ethyl-propoxy)-4,6- dimethoxy-isophthalic acid diethyl ester
The autoclave was charged with 38.21 g l,5-dibromo-3-(l-ethyl-propoxy)-2,4-dimethoxy-benzene (0.10 mol), 39.26 g potassium acetate (0.40 mol), 200 ml ethanol, 0.11 g palladium(II)acetate (0.5 mmol) and 0.25 g l,3-bis(diphenylphosphino)propane (0.6 mmol). The autoclave was sealed, pressurized and vented four times with 10 bar of carbon monoxide with stirring (200 rpm) and finally the reaction mixture was heated to 110°C with stirring (600 rpm). The CO pressure was adjusted to 10 bar and the reaction was continued at constant pressure (10 bar at 110°C) for 15 h. After cooling down, the autoclave was vented and the reaction mixture poured to a stirred mixture of 100 ml

hexane and 200 ml 5% aqueous Na2C03. The aqueous layer was separated and extracted with 100 ml hexane. Both organic layers were washed sequentially with 100 ml IN HCl, combined and dried over ca. 10 g Na2SO4. After filtration and removal of the solvent by rotary evaporation (50°C/> 1 mbar) the resulting 35.7 g yellow, oily residue were distilled on the high vacuum, affording 34.9 g (94.6%) of the title product as a light yellow oil, bp. 140°C/0.02 mbar.
Example 5
Preparation of rt//-a"s-5-(l-ethyl-propoxy)-4,6-dimethoxy-cyclohexane-l,3-dicarboxyHc
acid diethyl ester
The autoclave was charged with 36.84 g 5-(l-ethyl-propoxy)-4,6- dimethoxy-isophthalic acid diethyl ester (0.10 mol), 36.84 g 5% RU/AI2O3 catalyst and 250 ml ethyl acetate. The autoclave was sealed and pressurized three times under stirring with 5 bar of H2. The reaction mixture was then stirred under a pressure of 100 bar H2 at 60°C for 24 h. After cooling to room temperature, the autoclave was vented and flushed with argon. The black suspension was filtered over ca. 50 g filter aid (Hyflo) and the autoclave as well as the filtercake were washed with ca. 200 ml ethyl acetate. The combined, colorless filtrate was evaporated by rotary evaporation (50°C/> 1 mbar) affording 35.1 g (93.7%) solid, which was dissolved in 530 ml hexane at 50°C. Crystallization by cooling down and stirring at -20°C for 6 h afforded, after filtration, washing with ca. 50 ml -20°C cold hexane and drying (50°C/1 mbar/16h) 30.8 g (82.2%) white crystalline tide product, mp. 108-109°C.
Example 6
Preparation of fl//-c/5-5-(l-ethyl-propoxy)-4,6-dihydroxy-cyclohexane-l,3-dicarboxylic
acid diethyl ester
To a suspension of 60.0 g sodium iodide (0.40 mol) in 200 ml acetonitrile were added 0.360 g deionised water (0.02 mol). After stirring at 40°C for 30 min. 50.6 ml trimethylchlorosilane (0.40 Mol = 43.5 g) were added all at once and stirring at 40°C was continued for 1 h. 37.4 g all-cis-5-(l-ethyl-propoxy)-4,6-dimethoxy-cyclohexane-l,3-

dicarboxylic acid diethyl ester (0.10 mol) were added to the white suspension all at once and stirring at 40° C was continued for 14 h. After cooling to room temperature, the orange suspension was distributed between 500 ml ethyl acetate and 250 ml deionised water while the two layers were decolorized by the addition of ca. 2.5 g sodium thiosulfate. The organic layer was washed twice with 100 ml, a total of 200 ml 10% brine and all three aqueous layers were extracted sequentially with 100 ml ethyl acetate. The combined organic layers were dried over ca. 25 g Na2SO4, filtered and the solvent was evaporated by rotary evaporation (50°C/> 10 mbar). The white, crystalline residue (34.9 g) was dissolved in 200 ml refluxing methylcyclohexane and crystallized by cooling down and stirring at -20°C for 16 h. Filtration and washing with ca. 20 ml -20°C cold methylcyclohexane afforded after drying (50°C/10 mbar/16h) 33.6 g (97.0%) white title product, mp. 115-116.5°C.
Example 7
Preparation of a//-cw-(lR,3S,4S,5S,6R)-5-(l-ethyl-propoxy)-4,6-dihydroxy-cyclohexane-l,3-dicarboxylic acid 1-ethyl ester
A suspension of 34.40 g all-cis-5-(l-ethyl-propoxy)-4,6-dihydroxy-cyclohexane-l,3-dicarboxylic acid diethyl ester (0.10 mol) in 390 ml 10 mM Tris-buffer pH 8.0 was heated to 35°C under vigorous stirring. 3.44 ml pig liver esterase ("technical grade" Roche Diagnostics) were added and the suspension kept at pH 8.0 and 35°C by the controlled addition (pH-stat) of 1.0 N sodium hydroxide solution under vigorous stirring. After a total consumption over 46 h of 103.3 ml 1.0 N NaOH (1.04 equivalents), the pH of the solution was adjusted to 2.0 with ca. 13 ml 25 % HCl. The reaction mixture was extracted three times with 330 ml dichloromethane and the combined organic layers were dried over ca. 100 g Na2SO4. After filtration and removal of the solvent by rotary evaporation (40°C/> 5 mbar) the residue was dried on the vacuum over night (0.03 mbar) affording 29.52 g (93.4 %) of the title product as a colorless gum, which was used without purification in the next step.
[a]D = + 7.2°(CHCl3;c = l)

Example 8
Preparation of (3aS,5R,6R,7R,7aS)-7-(l-ethyl-propoxy)-6-hydroxy-2-oxo-octahydro-benzooxazole-5-carboxylic acid ethyl ester
To a solution of 31.2 g all-cis-(lR,3S,4S,5S,6R)-5-(l-ethyl-propoxy)-4,6-dihydroxy-cyclohexane-l,3-dicarboxylic acid 1-ethyl ester (0.10 mol) in 200 ml dichloromethan"e were added 10.1 g triethylamine (0.10 mol) and 29.0 g diphenyl phosphoryl azide (0.10 mol). The clear reaction mixture was then stirred under reflux for 16 h. After cooling down it was distributed between 200 ml dichloromethane and 300 ml IM HCl. The organic layer was washed with 300 ml 5% NaHCOj and three times with 300 ml, 5% brine. The aqeous layers were extracted sequentially twice with 200 ml, dichloromethane. The combined organic layers were dried with ca. 50 g Na2SO4, filtered and the solvent was evaporated by rotary evaporation (35°C/> 10 mbar). The white, crystalline residue (34.6 g) was dissolved in 300 ml refluxing butyl acetate and crystallized by cooling down an stirring at -20°C for 16 h. Filtration and washing with ca. 40 ml -20°C cold butyl acetate afforded after drying (50°C/10 mbar/16h) 25.4 g (80.5% over two steps) white, crystalline title product, mp. 180-181°C.
[a]D = + 31.2°(CHCl3;c = l)
Example 9
Preparation of (3R,4S,5S)-5-tert.-butoxycarbonylamino-3-(l-ethyl-propoxy)-4-hydroxy-
cyclohex-1-ene carboxylic acid ethyl ester
To 2.40 g di-tert.-butyl dicarbonate (11 mmol), 25 mg 4-dimethylaminopyridine (0.2 mmol) and 3.15 g (3aS,5R,6R,7R,7aS)-7-(l-ethyl-propoxy)-6-hydroxy-2-oxo-octahydro-benzooxazole-5-carboxylic acid ethyl ester (10 mmol) were added 50 ml toluene and the suspension was stirred at room temperature for 4 h. The solvent was removed by rotary evaporation (50°C/10 mbar) and the gummy residue was redissolved in 50 ml toluene.

After the addition of 1.15 g tetramethylguanidine (10 mmol) the reaction mixture was refluxed for 20 h, cooled to room temperature and washed with 20 ml 2N HCl and twice with 20 ml, a total of 40ml 10% brine. The aqueous layers were extracted sequentially with 25 ml toluene, the organic layers were combined and dried over Na2SO4. Filtration and rotary evaporation (50°C/10 mbar) gave 3.80 g crystalline residue, which was dissolved in 70 ml hot hexane (60°C) and crystallized by cooling down and stirring over night at -20°C. Filtration and washing with ca. 10 ml -20°C cold hexane afforded after drying (50°C/10 mbar/16h) 2.88 g (77.6%) white, crystalline title product, mp. 102-102.5°C.
[aJD = -52.5° (CHCb; c = 1)
Example 10a
Preparation of (3R,4S,5S)-5-tert.-butoxycarbonylamino-3-(l-ethyl-propoxy)-4-trifluoromethanesulfonyloxy-cyclohex-1-enecarboxylic acid ethyl ester
A solution of 3.71 g (3R,4S,5S)-5-tert.-butoxycarbonylamino-3-(l-ethyl-propoxy)-4-hydroxy-cyclohex-1-ene carboxylic acid ethyl ester) (10 mmol) and 1.61 ml pyridine (20 mmol) in 20 ml CH2CI2 was cooled to 0°C. 1.73 ml trifluoromethanesulfonic anhydride (10.5 mmol) were added over 10 min. and stirring at 0°C was continued for 1 h. The reaction mixture was washed with 10 ml IN HCl and twice with 10 ml, a total of 20 ml 10% brine. The aqueous layers were extracted sequentially with 10 ml methylene chloride and the combined organic layers were dried over Na2SO4. Filtration and rotary evaporation (30°C/10 mbar) gave 4.96 g (98.4%) beige, cristalHne title product, which was used without ftirther purifcation in the next step.

Example 10b
Preparation of (3R,4S,5S)-5-tert.-butoxycarbonylamino-3-(l-ethyl-propoxy)-4-trifluoromethanesulfonyloxy-cyclohex-1-enecarboxylic acid ethyl ester
To 4.80 g di-tert.-butyl dicarbonate (22 mmol), 49 mg 4-dimethylaminopyridine (0.4 mmol) and 6.31 g (3aS,5R,6R,7R,7aS)-7-(l-ethyl-propoxy)-6-hydroxy-2-oxo-octahydro-benzooxazole-5-carboxylic acid ethyl ester (20 mmol) were added 100 ml toluene and the suspension was stirred at room temperature for 4 h. After the addition of 20 mg 60% sodium hydride dispersion in oil (ca. 0.5 mmol), the reaction mixture was refluxed for 1 h, cooled to room temperature and the solvent was removed by rotary evaporation. The yellowish, semicrystalline crude (3R,4S,5S)-5-tert.-butoxycarbonylamino-3-(l-ethyl-propoxy)-4-hydroxy-cyclohex-l-ene carboxylic acid ethyl ester (7.83 g) was redissolved in 100 ml CH2CI2 and 3.22 ml pyridine (40 mmol) were added under stirring. After cooling to -10°C, 3.47 ml trifluoromethanesulfonic anhydride (21 mmol) were added by a syrringe over 10 min and stirring at -10°C was continued for 1 h. 20 ml IN HCl were added to the -10°C cold reaction mixture under stirring and the organic layer was washed twice with 20 ml, a total of 40 ml 10% brine. All aqueous layers were extracted sequentially with 20 ml CH2CI2 and the combined organic layers were dried over Na2SO4, filtered and the solvent was removed by rotary evaporation (30°/>10 mbar). The yellow, crystalline residue (10.0 g) was dissolved in 150 ml hot diisopropyl ether (68°C) and transferred into a new flask. After cooling to room temperature the suspension was stirred over night at -20°C. Filtration and washing with ca. 40 ml -20°C cold diisopropyl ether afforded after drying (50°C/10 mbar/16h) 8,35 g (82.9%) white, crystalline title product, mp. 122-123°C.
[a]D = -79.1°(CHCl3;c=l)
Example 11
Preparation of (3R,4R,5S)-4-azido-5-tert.-butoxycarbonylamino-3-(l-ethyl-propoxy)-
cyclohex-1-enecarboxylic acid ethyl ester

To a stirred suspension of 10.07 g (3R,4S,5S)-5-tert.-butoxycarbonylamino-3-(l-ethyl-propoxy)-4-trifluoromethanesulfonyloxy-cydohex-l-enecarboxylic acid ethyl ester (20 mmol) and 50 ml 90% aqueous acetone were added 1.43 g sodium azide (22 mmol) and the reaction mixture was stirred at room temperature for 15 h. The acetone was removed by rotary evaporation (40°C/>10 mbar) and the oily residue was distributed between 50 ml ethyl acetate and 25 ml 5% brine. The aqueous layer was extracted with 25 ml ethyl acetate and both organic layers were washed sequentially with 25 ml 5% brine. The combined organic layers were dried (Na2SO4) and the solvent was removed by rotary evaporation (40°C/>10 mbar) affording 8.00 g light yellow, oily residue, which was dissolved in 80 ml hot hexane (50-60°C), filtered and crystallized by cooling down and stirring at -20°C over night. Filtration and washing with ca. 20 ml -20°C cold hexane afforded after drying " (50710 mbar/16h) 6.15 g (77.6%) white, crystalline title product, mp. 92-93°C.
[a]D = -63.3°(CHCl3;c=l)
Example 12
Preparation of (3R,4R,5S)-4-acetylamino-5-tert.-butoxycarbonylamino-3-( 1-ethyl-propoxy)-cyclohex-l-ene carboxylic acid ethyl ester
A solution of 1.59 g (3R,4R,5S)-4-azido-5-tert.-butoxycarbonylamino-3-(l-ethyl-propoxy)-cyclohex-l-enecarboxylic acid ethyl ester (4 mmol) and 0.36 ml water (20 mmol) in 5 ml tetrahydrofurane was cooled to 0°C. 1.12 ml triethylamine (8 mmol) and 0.38 ml acetic anhydride were added and stirring at 0°C was continued for 15 min.1.14 ml tri-n-butyl phosphine (4.4 mmol) were added over 5 min. and the yellowish solution was stirred for 30 min. at 0°C and then for 1 h at room temperature. After the addition of 5.58 ml triethylamine (40 mmol) 1.89 ml acetic anhydride (20 mmol) were added slowely under ice cooling and stirring at room temperature was continued for 1 h. The reaction mixture was diluted with 30ml ethyl acetate and washed sequentially with 25 ml 2N HCl, 10 ml 10% Na2C03 and 20 ml 10% brine. The aqueous layers were extracted sequentially with 20 ml ethyl acetate. The combined organic layers were dried (Na2SO4) and the solvent was removed by rotary evaporation (30°C/>10 mbar) affording 2.89 g crude, which was purified by chromatography on Si02 (100 g) with hexane ethyl acetate 1.4 : 1 (100 ml

fractions). Rotary evaporation (30°C/>10 mbar) gave 1.39 g (84%) of the title product as a colorless, crystalline residue, mp. 153.5-154.5°C.
[a]D = -89.7° (CHCI3; c = 1)
Example 13a
Preparation of (3R,4R,5S)-4-acetylamino-5-amino-3-(l-ethyl-propoxy)-cyclohex-l-enecarboxylic acid ethyl ester phosphoric acid salt
To a solution of 10.31 g (3R,4R,5S)-4-acetylamino-5-tert.-butoxycarbonylamino-3-(l-ethyl-propoxy)-cyclohex-l-enecarboxylic acid ethyl ester (25 mmol) in 100ml ethyl acetate were added at room temperature. 25 ml 5N HCl in ethyl acetate. After 20 min. a white precipitate was formed and the thick suspension was stirred at room temperature for 24 h. The suspension was diluted with 125 ml ethyl acetate, washed with ca. 40 ml 3N NaOH (pH ca. 9.5) and 50 ml 10% brine. The aqueous layers were extracted sequentially twice with 125 ml, a total of 250 ml ethyl acetate. The combined organic layers were dried (Na2SO4) and the solvent was removed by rotary evaporation (30°C/>10 mbar) affording 8.06 g (3R,4R,5S)-4-acetylamino-5-amino-3-(l-ethyl-propoxy)-cyclohex-l-enecarboxylic acid ethyl ester which was dissolved in 50 ml ethanol and added over ca. 2h to a warm solution (55°C) of 2.45 g 99% phosphoric acid (25 mmol) in 50 ml ethanol. (After the addition of ca. 2/3 of (3R,4R,5S)-4-acetylamino-5-amino-3-(l-ethyl-propoxy)-cyclohex-l-enecarboxylic acid ethyl ester, the clear solution was seeded with pure title product). After cooling down and stirring at 0-5°C for 3 h, the suspension was filtered, washed twice with 40 ml, a total of 80 ml acetone and dried (50°C/10 mbar/16h) affording 9,07 g (88.4%) white, crystalline title product, mp. 201-202°C.
[a]D = -32.1°(H20;c=l)

Example 13b
Preparation of (3R,4R,5S)-4-acetylamino-5-amino-3-(l-ethyl-propoxy)-cyclohex-l-enecarboxylic acid ethyl ester phosphoric acid salt
To a solution of 3.96 g (3R,4R,5S)-4-azido-5-tert.-butoxycarbonylamino-3-(l-ethylpropoxy)cyclohex-l-enecarboxylic acid ethylester (10 mmol) in 50 ml ethyl acetate were added 2.0 g wet Raney-Cobalt catalyst and the suspension was stirred and hydrogenated at room temperature for 20 h (-1.1 bar H2; 500 rpm). After removing the catalyst by filtration, 1.53 ml triethylamine (11 mmol =1.11 g) and 0.99 ml acetic , anhydride (10.5 mmol = 1.07 g) were added all at once and the colorless solution was stirred at room temperature for 1 h.Then 5.26 ml 5.7 M HBr/acetic acid (30 mmol HBr) were added to the colorless solution and the reaction mixture was stirred at room temperature for 20 h. Then ca. 55 ml 2 N NaOH (pH ca. 9.5) were added under stirring and the organic layer was separated and washed twice with 30 ml, a total of 60 ml 20% brine. All three aqueous layers were extracted sequentially and twice with 30 ml, a total of 60 ml ethyl acetate and the combined organic layers were dried (Na2SO4). After filtration and removal of the solvent by rotary evaporation (50°/> 1 mbar) the yellowish, viscous residue (3.47 g) was dissolved in 20 ml ethanol and added under stirring to a 50°C warm solution of 0.98 g ortho-phosphoric acid (10 mmol) in 40 ml ethanol over 30 min (after the addition of two third, the 50°C warm solution was seeded with pure title product). The white suspension was cooled down (2 h) and stirred at 0°C for 3 h. The crystals were filtered, washed with ca. 20 ml acetone and dried (50710 mbar/16h) affording 3.41 g (83.2%) white, crystalline phosphoric acid salt, mp. 198-199°C (dec).
[a]D = -32.1°(H20;c=l)
Example 14
Preparation of rt//-d5-(lS,3R,4R,5R,6S)-5-(l-ethyl-propoxy)-4,6-dimethoxy-cyclohexane-l,3-dicarboxylic acid 1-ethyl ester)
To a suspension of 74.9 g all-cis-5-(l-ethyl-propoxy)-4,6-dimethoxy-cyclohexane-l,3-dicarboxylic acid diethyl ester (0.20 mol) in 240 ml cyclohexane was added 1.11 0.1 M glucose in water and 60 ml 0.1 M sodium phosphate buffer pH 7.0, and the mixture was heated to 35°C under vigorous stirring. 560 mg Lipase from Aspergillus oryzae (Fluka

62285) was added and the emulsion/suspension kept at pH 7.0 and 35°C by the controlled addition (pH-stat) of 1.0 N sodium hydroxide solution under vigorous stirring. After a total consumption of 187.5 ml 1.0 N sodium hydroxide (0.94 equivalents) after 20 h the pH was set to 2.0 with ca. 200 ml 1 N hydrochloric acid and the reaction mixture extracted with 1.5 1 dichloromethane. The whole emulsion was filtered through a bed of 150 g dicalite filter aid and the aqueous phase extracted again with 2x1.5 1 dichloromethane which were passed through the dicalite bed before use. The combined organic phases were dried on 175 g Na2SO4, filtered, concentrated (13mbar/50°C/lh) and the residue dried overnight on a high vacuum to give 69.42 g (100%) white crystalline title product, mp. 147-148°C.
[a]D = +7.4°(CHCl3;c=l)
Example 15
Preparation of all-cis-(lS,3R,4R,5R,6S)-5-(l-ethyl-propoxy)-4,6-dihydroxy-cycIohexane-l,3-dicarboxylic acid 1-ethyl ester)
To a stirred suspension of 30.0 g sodium iodide (0.20 mol) in 100 ml acetonitrile were added 21.7 g trimethyl-chlorsilane (0.20 mol; 25.3 ml) all at once. After stirring at room temperature for 0.5 h 17.3 g all-cis-5-(l-ethyl-propoxy)-4,6-dimethoxy-cyclohexane-l,3-dicarboxylic acid 1-ethyl ester (0.050 mol) were added and stirring at room temperature was continued for 12 h. The reaction mixture was distributed between 250 ml dichloromethane and 250 ml deionized water. After the two reddish phases were decolorized by the addition of ca. 0.25 g Na2S2O3, the organic layer was washed twice with 100 ml, a total of 200 ml 10% brine. All aqueous layers were then extracted sequentially with 100 ml dichloromethane. The combined organic layers were dried over Na2SO4, filtered and the solvent was evaporated by rotary evaporation (50°C/> 1 mbar) affording 15.8 g (99.4%) of the title product as a colorless gum, which was used without purification in the next step.
[a]D = -7.2o(CHCl3;c=l)

Example 16
Preparation of all-cis-(lS,3R>4R,5R,6S)-7-(l-ethyl-propoxy)-6-hydroxy-2-oxo-octahydro-
benzooxazole-5-carboxylic acid ethyl ester
To a solution of 15.77 g all-cis-(lS,3R,4R,5R,6S)-5-(l-ethyl-propoxy)-4,6-dihydroxy-cyclohexane-l,3-dicarboxylic acid 1-ethyl ester (50 mmol) in 100 ml dichloromethane were added 5.06 g triethylamine (50 mmol) and 14.48 g diphenyl phosphoryl azide (50 mmol). The clear reaction mixture was then stirred under reflux for 16 h. After cooling down it was distributed between 100 ml dichloromethane and 150 ml IM HCl. The organic layer was washed with 150 ml 5% NaHCO3 and three times with 150 ml, a total of 450 ml 5% brine. All five aqeous layers were extracted sequentially twice with 100 ml,"a total of 200 ml dichloromethane. The combined organic layers were dried with ca. 25 g Na2SO4, filtered and the solvent was evaporated by rotary evaporation (35°C/> 10 mbar). The white, crystalline residue (17.4 g) was dissolved in 150 ml refluxing butyl acetate and crystallized by cooling down and stirring at -20°C for 16 h. Filtration and washing with ca. 20 ml -20°C cold butyl acetate afforded after drying (50°C/10 mbar/16h) 12.6 g (79.9% over three steps) white, crystalUne title product, mp. 180.5-181°C.
[a]D = -31.1°(CHCl3;c=l)

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Patent Number 209362
Indian Patent Application Number 305/MAS/2001
PG Journal Number 38/2007
Publication Date 21-Sep-2007
Grant Date 27-Aug-2007
Date of Filing 09-Apr-2001
Name of Patentee M/S. F. HOFFMANN-LA ROCHE AG
Applicant Address 124 Grenzacherstrasse, CH 4070 Basle
Inventors:
# Inventor's Name Inventor's Address
1 HANS IDLING 25 Hauptstrasse, D-79618 Rheinfelden,
2 BEAT WIRZ 4 Wiedenweg, CH-4153 Reinach
3 ULRICH ZUTTER 33 Socinstrasse, CH-4051 Basle
PCT International Classification Number C07C231/00
PCT International Application Number N/A
PCT International Filing date
PCT Conventions:
# PCT Application Number Date of Convention Priority Country
1 00107669.4 2000-04-10 EUROPEAN UNION