Brief description of the invention The present invention relates to a new process for preparing (S)- (+)-2- (substituted phenyl)-2-hydroxy-ethyl carbamates and to novel intermediates used in this process.

It further relates to polymorphic forms of said carbamates.

Background of the Invention 2- (Substituted phenyl)-2-hydroxy-ethyl carbamates and their isomers have been described in US-5,698, 588 and in US-5,854, 283, which corresponds to WO-97/26241, as compounds useful for treating disorders of the central nervous system in particular convulsions, epilepsy, stroke, muscle spasms, neuropathic pain and migraine. These compounds have an asymmetric carbon atom at the benzylic position, which is the aliphatic carbon atom adjacent to the phenyl ring. This asymmetric carbon atom preferably is in an S-configuration. A preferred compound among these carbamates is (S) - (+) -2- (2-chlorophenyl) -2-hydroxy-ethyl carbamate, which compound is also referred to as RWJ-333369. This and similar optically pure forms of carbamates of halogenated 2-phenyl-1, 2-ethanediol have been described in US-6,127, 412 and US- 6,103, 759.

These compounds are prepared by reacting the appropriately substituted phenyl-1,2- ethanediol with dimethylcarbonate thus yielding the corresponding phenyl-1,2- ethanediol carbonate which subsequently was reacted with a suitable amine which yielded two regioisomeric forms of the resulting carbamates which had to be separated by column chromatography. Stereoisomerically pure compounds were prepared similarly, starting from the enantiomerically pure starting material. This process results

in a mixture of two regioisomeric products, one of which needs to be removed, which has a negative impact on the yield. Both regioisomeric end products are separated by chromatography which is a cumbersome procedure, especially in large scale production.

It is an object of this invention to provide a process that not only avoids this separation step and concomitant loss of undesired regioisomer, but also results in end product in high yield and purity, in particular in high enantiomeric purity. A further object is to provide a process that can be scaled up to large production batch sizes, to provide a process that uses starting materials that are easy to produce or are commercially available. It is still a further object to provide a process that is cost-effective and does not give rise to side products that are hazardous or difficult to remove. It is another object of the present invention to provide a process that has a limited number of purification steps, in particular a process wherein some or all of the intermediates need no purification. A still further object is to provide a process that avoids excess quantities of starting materials and solvents.

These objects are attained by the process of the present invention.

Drug substances, also referred to as active pharmaceutical ingredients, can occur as polymorphic forms. In almost all instances, a particular polymorphic form has different properties compared to the active ingredient not occurring in a specific polymorphic form or compared to another polymorphic form of an active ingredient. Properties may differ as far as solubility, stability, flowability, tractability, compressibility, etc. , are concerned. These differences in turn are known to affect the properties of the formulations made of such active ingredients as well as the final or finished dosage forms thereof. Authorities responsible for drug approval in many countries require the complete characterization of the active ingredient used in each drug product, including the identification and control of polymorphic forms. If present in the finished product, drug approving authorities require the manufacturer of the active substance, in the least, to control its synthetic processes such that the percentages of the various respective polymorphic forms, when present, are consistent among batches and within the drug

substance's approved specifications. Left uncontrolled in synthetic processes, the percentage of a given polymorph can fluctuate therefore having an effect of the properties of the active substance and the finished drug product such that it no longer meets the specifications of the drug approval. Therefore a robust control is required of the synthetic process specifications and of the end product, in particular as far as the presence of consistent amounts of polymorphic forms is concerned.

Many active substances do not show polymorphism and the presence of polymorphic forms of a new chemical active ingredient is not readily predictable. Variations in the process parameters can lead to varying degrees of the presence of polymorphic forms in end products, which, as explained above is undesirable. Therefore the knowledge of the presence of polymorphic forms and their characterization is a highly desirable goal to achieve.

Quite unexpectedly it has now been found that (S)- (+)-2- (substituted phenyl)-2- hydroxy-ethyl carbamates occur as polymorphic forms that can be isolated and characterized. In an additional aspect, this invention provides practical and reproducible procedures to prepare these polymorphic forms.

Summary of the Invention The present invention relates to a process of preparing a compound of formula (I) : wherein: R is halo;

R1 and R2 independently are hydrogen or C1-4alkyl, optionally substituted with phenyl or substituted phenyl, wherein substituted phenyl has substituents selected from halogen, Cl-4alkyl, Cl_4alkyloxy, amino, nitro and cyano; characterized by (a) reducing an ester of formula:

wherein: P is an appropriate alcohol-protecting group; R3 is Cl 4alkyl ; with an appropriate ester-to-alcohol reducing agent, thus obtaining an alcohol of formula :

(b) reacting the alcohol of formula ( with a carbonyl compound of formula

wherein X and Y are appropriate leaving groups; and subsequently with an amine of fonnula

thus obtaining a compound of fonnula :

(c) removing the protecting group P thus obtaining a compound of formula (I).

In some instances one or more of the substituents R1, R2 and R3 may have asymmetric carbon atoms and hence may cause the compounds of formula (I) to occur in

stereoisomeric forms. Such stereoisomeric forms are intended to be embraced within the scope of the present invention.

Preferred compounds of formula (I) are those wherein R is 2-chloro, R1 and R2 are hydrogen.

The group P is an appropriate alcohol protecting group. Preferred groups P are of the ether type. A particularly preferred protecting group P is 2- (2-methoxy) propyl.

In a preferred execution of the process the carbonyl compound of formula (IV) is selected from 1, l'-carbonyl-diimidazole and phenyl chloroformiate.

A particular execution of the process is that wherein R3 is methyl.

Another particular execution of the process is that wherein the appropriate ester-to- alcohol reducing agent is a metal hydride or a complex metal hydride.

In a further aspect the invention relates to a compound of formula wherein R, R1 and R2 are as defined in claims 1 or 2 and P is an appropriate hydroxy- protecting group.

In another aspect, the invention relates to a compound of formula

wherein R is as defined in claims 1 or 2 and P is an appropriate hydroxy-protecting group.

In still another aspect the invention relates to a compound of formula wherein R is as defined in claims 1 or 2, R3 is Cl 4alkyl ; and P is an appropriate hydroxy-protecting group.

Preferred are those compounds of formulae (IV), (m) or (In wherein P is 2- (2- methoxy) propyl.

Also preferred are those compounds of formula (II) wherein R3 is methyl.

In still another aspect, the invention relates to a process for preparing a compound of formula (VI) characterized by process steps (a) and (b) as outlined above.

In still another aspect, the invention relates to a process for preparing a compound of formula (m) characterized by process step (a) as outlined above.

In still another aspect, the invention relates to a process for preparing a compound of formula (In characterized by process steps (d) and (e) as outlined hereinafter.

The invention further provides a process preparing a compound of formula (I) characterized by process steps (d) and (e) as outlined hereinafter and by process steps (a), (b) and (c) as outlined above.

In a further aspect, this invention concerns the presence of polymorphic forms of the (S) - (+) -2- (substituted phenyl) -2-hydroxy-ethyl carbamates. In particular it concerns two polymorphic forms of the compound 2- (2-chlorophenyl)-2- (2- (2- methoxy) propyl) -ethyl carbamate The invention also concerns processes for preparing these new polymorphic forms.

Detailed Description of the Invention Subject of the present invention is a process for preparing compounds of formula (I), as outlined above, and the intermediates of formula (II), (m), (IV), and (V) as represented and defined hereinabove.

Preferred are those compounds and intermediates as defined herein wherein R is 2- chloro, R1 and R2 are hydrogen. The compound of formula (I) wherein the substituents have the latter meanings is also referred to as'RWJ-333369'and can be represented by the structural formula:

The term"halogen"refers to fluoro, chloro, bromo and iodo.

"Cl 4alkyl"defines straight and branched chain saturated hydrocarbon radicals having from 1 to 4 carbon atoms such as methyl, ethyl, 1-propyl, 2-propyl, 1-butyl, 2-butyl, 2- methyl-l-propyl, 2-methyl-2-propyl.

"C1_4alkyloxy"defines C1_4alkyl radicals linked to an oxygen atom such as methoxy, ethoxy, 1-propoxy, 2-propoxy, 1-butoxy, 2-butoxy and the like.

"Substituted phenyl"is phenyl being substituted with the substituents outlined above.

Preferably, substituted phenyl has 1,2 or 3 substituents. A preferred substituent is halogen, more preferably chloro.

P, as mentioned above, is an appropriate hydroxy protecting group. Preferably it should be selected such that it is stable in the reduction procedure of (IT) to (In) as well as the subsequent reaction step from (E) to (VI). The preferred reduction procedure being with complex hydrides as outlined hereinafter, the group P should be stable towards these complex hydrides and the reaction products therefrom. The reduction with complex hydrides requires basic conditions and hence the group P should not be cleaved in these basic conditions. The group P should preferably be removable under acidic conditions which should be such that the carbamate function is not split.

Particularly preferred are protecting groups P that are removable at a pH which is about 1 or slightly higher.

Particularly useful are groups P of the ether type. As examples of P there may be mentioned: methoxymethyl ethers (MOM): which can be prepared from methoxymethylchloride or formaldehyde dimethylacetal; tetrahydropyran ethers (THP ethers) prepared from dihydropyran; tetrahydrothioypyranyl ethers from dihydrothiopyran; chloro substituted tetrahydrofuranyl ethers from 2-chlorotetrahydrofuran; tetrahydrothiofuranyl ethers from dihydrothiofuran ;

1-ethoxyethyl ethers from ethylvinyl ethers or 1-ethoxyethyl chloride 1-methyl-1-methoxyethyl ethers from methylvinyl ethers, which are of particular interest; triphenyl ethers and appropriate derivatives thereof which can be prepared from the corresponding chlorides; benzyl ethers and appropriate derivatives thereof which can be prepared from the corresponding bromides or iodides; 4-methoxytetrahydropyranyl ethers from 5,6-dihydro-4-methoxy-2H-pyran ; 4-methoxytetrahydrothiopyranyl ethers from 5, 6-Dihydro-4-methoxy-2H- thiopyran.

It is furthermore advantageous to use such groups P which do not lead to a mixture of diastereomers, i. e. P groups without an asymmetric center. Under certain circumstances, e. g. depending upon the nature of the reducing agent, particular silyl ethers can be used as appropriate groups P, in particular t. butyldimethylsilyl (TBDMS), triisopropylsilyl, tribenzylsilyl, and the like.

Step (a) : preparation of 2-(substituted phenyl !-2-(protected hydroxy !-ethanol (m) According to the first step of the process of this invention, the ester (In is reduced to the corresponding alcohol of formula (III) using an appropriate ester-to-alcohol reducing agent. The latter may be a metal hydride or a complex metal hydride such as lithium aluminium hydride or derivatives thereof.

Particular reduction agents for this reaction are silane agents such as trialkylsilanes, dialkylsilanes, trialkoxysilanes and preferably poly methylhydrogensiloxane ('PMHS') in the presence of a suitable catalyst. The latter in particular are transition metal halogenides or carboxylates, and preferably the latter is a zinc carboxylate, such as zinc hexanoate or a derivative thereof, more preferably zinc 2-ethylhexanoate, in the presence of a metal hydride such as an alkali metal or earth alkaline metal hydride, or aluminium hydride, e. g. lithium, sodium, potasium, calcium hydride, or a complex hydride such as a borohydride or aluminium hydride, in particular an alkali metal borohydride or aluminiumhydride, e. g. lithium, sodium or potassium borohydride or

aluminium hydride. A combination of zinc 2-ethylhexanoate and sodium borohydride is most preferably used as the catalyst mixture. These and similar reduction agents are described in Patent Application WO 96/12694 (1995) and in J. Ulman, The Alembic, 1999, 59, 1 ff.

The reaction of this process step is conducted in a suitable solvent, e. g. an ether or polyether, or a hydrocarbon, in particular an aromatic hydrocarbon. Specific examples of suitable solvents comprise diethyl ether, dipropyl ether, diisopropyl ether, dibutyl ether, diglyme and toluene.

The reduction agent can be formed by stirring a mixture of the agents ERS A and ERS B in a separate reaction vessel (ERS = Ester Reduction System), commercially available from Rohm & Haas). ERS A is a solution of NaBH4 in tetraglyme, whereas ERS B is a solution of Zn (carboxylate) 2*H20, in particular of Zn (2-ethylhexanoate) 2 *H20, in tetraglyme. ERS A and ERS B are preferably mixed at higher temperature, e. g. at a temperature in the rage of 50 to 90°C, in particular at 70°C for a period of several minutes, e. g. for 30 min. Subsequently the ERS A and ERS B mixture is added to the ester (IT) and ERS C is added. ERS C is poly methylhydrogensiloxane.

The reducing agent can also be generated in situ in the reaction vessel, which is particularly attractive. In this variant, intermediate (II) is dissolved in a suitable solvent, preferably in toluene at increased temperature of 80-90°C. ERS B is added first in one portion, followed by the addition of ERS A also in one portion. Then immediately ERS C is added within one hour while controlling the temperature and keeping it at higher temperature, in particular around 95°C.

The starting mandelic acid ester (IT) is prepared as described hereinafter and can be isolated and optionally purified and used as such in the reduction step. The ester (Il) can also be kept dissolved in the solvent in which it was prepared and used as such in the reduction step.

Preferably the substituted mandelic acid ester (IT) is a methyl ester.

In a particular execution of this process step the starting ester (II) is either used dissolved in the solvent of the previous reaction step, or it can also be solved in a suitable solvent, such as for example an ether, e. g. in di-n-butylether, or preferably in toluene. The reducing agent, prepared as above, is added in one portion to the solution, followed by the addition of ERS C within one hour. The reaction mixture optionally can be heated to 90°C prior to addition of ERS C. Then the temperature is increased to 90°C and kept at that temperature until an in-process-control shows a conversion of at least 99%. The reaction time is around 1 h. After complete reduction the mixture is cooled to 15 to 20°C and hydrolyzed carefully first with methanol and subsequently with aqueous alkali metal hydroxide solution, which preferably is a NaOH solution in slight excess (e. g. 1.3 mol-eq. , using a 30% solution).

Subsequently, the mixture is refluxed for about 1 h at about 50°C and the layers are separated at room temperature. The organic layer is washed with water and with saturated aqueous NaCl at room temperature.

The quantity of ERS C is in the range of 2 to 4, in particular in the range of 2.2 to 3 molar equivalents, preferably 2.3 molar equivalents of ERS C are used.

The reaction typically is complete after about 1 hour.

After completion of the reduction reaction, the excess of ERS C can be destroyed with a suitable ester, in particular with ethyl acetate. After addition of the said ester, the mixture is stirred for one hour and hydrolyzed at 90°C by addition of aqueous base solution, preferably a NaOH or a KOH-solution (e. g. of 33%) and further preferably with the use of methanol. Further work-up comprises the separation of the organic layer and washing with aqueous basic solution (e. g. KOH-solution of 33%) and with water.

The resulting methylester is an oil, and, if desired, can be distilled for purification.

Step (b) : preparation of 2-(substituted phenyl !-2-(protected hedroxy !-ethyl carbamate (vu In this step the alcohol of formula (m) is reacted with a carbonyl compound of formula

wherein X and Y are appropriate leaving groups. Preferably one of X or Y is more reactive than the other. X and Y can be halogen, in particular chloro or bromo, but preferably X and Y are imidazolyl groups. If X is halo, Y preferably is an aryloxy or alkoxy group. In the latter instance (V) is an alkyl or aryl halo formiate. Particular aryl groups in (IV) are phenyl or substituted phenyl, e. g. halophenyl, or Cul-4 alkyl. A preferred example of (IV) is phenyl chloroformiate or 1, 1'-carbonyl-diimidazole.

The reaction is conducted in a suitable solvent such as a hydrocarbon, in particular an aromatic hydrocarbon, e. g. toluene, or in an ether, e. g. THF. The reaction temperature depends upon the reactivity of the reagent (IV) but in general is room temperature or lower. In case N, N'-carbonyl diimidazole is used as reagent the reaction preferably is conducted at room temperature (i. e.. at about 25 °C).

The reaction typically is complete after less than 1 hour, e. g. after about % 2 hour. The reaction product of this reaction is usually not isolated; it can be represented by the following formula : wherein Y is as defined hereinabove and in particular is an imidazolyl group, or an aryloxygroup, e. g. a phenoxy or substituted phenoxy group. The intermediates of

formula (IV-a) are deemed novel and constitute an additional feature of the present invention. Preferred intermediates of formula (IV-a) are those wherein Y is imidazol- 1-yl.

The product of the previous reaction, i. e. the intermediate of formula (IV-a), is usually not isolated and is reacted immediately with the amine of formula (V) as specified above. A preferred amine is ammonia, but it can also be an ammonium salt. In that instance the ammonia or an ammonium salt is in an aqueous medium and added to the solution of intermediate (IV-a) at room temperature.

Vigorous stirring is recommended when using (V) in aqueous media, because of the two phase system. The reaction is terminated after several hours, in particular after about 4 hrs. The organic phase is separated and the product can optionally be isolated and purified. The organic phase with product (VI) dissolved therein can also be used as such in the subsequent reaction step.

Step c: preparation of 2-(substituted phenyl !-2-hydroxYethYl carbamate (D This reaction step involves the deprotection of the hydroxy function and depends on the nature of the group P.

Where P is 2-methoxy-2-propyl, removal is by addition of an appropriate acid, e. g. hydrochloric acid.

In a preferred execution, product (VI) is used dissolved in the solvent of the previous step. Water and concentrated hydrochloric acid are added while stirring. Already after a few minutes the reaction is almost completed and the end procuct (I) starts precipitating. The reaction mixture is stirred for a couple of hours, in particular for about 4 hours because in this way the end product can be filtered better. Subsequently the end product is filtered off and washed.

The end product (I) can be recrystallized from a suitable solvent such as an alcohol, e. g. methanol, preferably with addition of acidified water.

Starting materials The starting materials (n) are obtained by a process which is characterized by: (d) an esterification reaction of an appropriately substituted mandelic acid of formula :

thus preparing the corresponding ester of formula

wherein in (VIII) and (IX) R and R3 are as defined above and R preferably is 2-chloro and/or R3 preferably is methyl; and (e) treating the ester (IX) with a suitable reagent generating a hydroxy protecting group, thus preparing an intermediate of formula

wherein R and P are as defined above.

The ester (IX) is reacted with an appropriate agent capable of introducing a hydroxy protecting group. A preferred agent is 2-methoxypropene.

Alternatively, the sequence of the above steps may be switched, i. e. the hydroxy protecting group may be introduced and subsequently the ester formed.

Step (d) : Preparation of substituted mandelic acid esters (IX) According to this reaction step the starting acid (VE) is reacted in the alcohol of which the ester (IX) is derived. Typically a CI-4 alkanol is used, preferably methanol, thus yielding the corresponding Cl 4 alkyl esters or preferably the methyl ester of (VE).

The reaction is conducted with an excess of a strong acid, preferably a hydrohalic acid such as HC1, in particular with 1-4 molar equivalents, preferably with 2.5 molar equivalents of concentrated HC1. The reaction also works with a catalytic amount of sulfuric acid or also with SOC12. In the latter instance the reaction is highly exothermic, requiring appropriate measures for controlling the temperature.

The reaction preferably is conducted at room temperature or slightly increased temperatures, preferably not higher than about 30°C. The reaction time usually is less than about 1 hour, e. g. about 30 min. The resulting ester (IX) typically is an oily compound which is used as such in the subsequent process steps. In a preferred execution, the ester (IX) is kept in the solvent in which it was made and is used further dissolved in this solvent.

Step (e) : Preparation of hydroxy-protected substituted mandelic acid esters (II).

The reaction conditions of this step depend on the nature of protecting group P.

In a preferred execution, P is 2-methoxy-1-propyl which is derived from 2-methoxypropene. The latter is dissolved in a suitable solvent, in particular the solvent in which the other reaction steps are conducted. This solution is added to a solution of intermediate (IX) in a suitable solvent which has been acidified, e. g. by addition of hydrochloric acid, in particular by adding gaseous hydrochloric acid over the solution. The pH should preferably be low, e. g. pH 1-2. The solvent of intermediate (IX) should preferably be the same as that wherein the 2-methoxypropene is dissolved and more preferably should be the same as the solvent used in the other reaction steps.

The reaction is complete in less than 1 hour, normally within half an hour.

The process according to the present invention yields the end product (I) in high yield and purity and can be scaled up to production size batches. A particular aspect of the current process is that it leaves the stereochemical integrity intact of the asymmetric center on the carbon atom bearing the hydroxy function, i. e. the present process shows neglectable or no racemisation.

The various intermediate products of the process, including the steps for preparing the starting materials, can be isolated and if desired further purified before further use in a next step. Alternatively, all the process steps, if desired also including the steps for preparing the starting materials, can be conducted in the same solvent, i. e. without isolation and optional purification of the intermediate products. In the latter instance it may be advantageous to distil off some of the solvent or to add some of it during one or more of the reaction steps. A suitable solvent for the one solvent execution of the process is an aromatic hydrocarbon, preferably toluene. It is also possible to conduct a certain number of steps in one solvent and the others in another.

Conducting the whole process in one solvent has the particular advantage that the process is much simpler and can be conducted more quickly without having to discard or recuperate solvents, which is advantageous economically as well as from an environmental aspect.

Polymorphes The present invention is further directed to novel crystalline structures of the compound of formula (I) wherein R is 2-chloro, Rl and R2 are hydrogen, said compound hereinafter being referred to as compound (I-a).

The crystalline forms of compound (I-a) may be prepared by an appropriate recrystallization of compound formula (I-a) from a suitable organic solvent. Depending upon the recrystallisation procedure either form A or form B can be obtained.

One crystalline form of compound (I-a) is referred to as'form A'and is prepared by recrystallisation of compound (I-a) from a suitable solvent. The temperature in this recrystallisation procedure is kept below 60 °C, in particular below 50 °C. Suitable solvents are those wherein the compound of formula (I-a) dissolves at higher temperature and is relatively poorly soluble at lower temperature, e. g. at a temperature lower than 20 °C, or lower than 10 °C, or even lower than 0 °C, or-10 °C. Suitable solvents are the lower alkanols, i. e. the Cl 4alkanols and in particular methanol.

In one type of embodiment, the compound (I-a) is dissolved by heating or refluxing in methanol, or by heating in a lower alkanol. The temperature of the mixture should not allowed to exceed 60 °C. Subsequently, the solution is cooled, preferably slowly, e. g. by simply allowing the solution to cool. At a temperature of about 50 °C crystallization already starts. The mixture is stirred at room temperature for 15-20 hours whereupon acidified water is added. The water preferably is acidified with a strong acid, e. g. hydrochoric acid or a similar acid to a pH value of about 3 to 4, in particular about pH 3.5. The mixture is further cooled to about 0 to 10 °C, in particular to about 5 °C and stirred at that temperature for a sustained period of time, e. g. about 1 hour. The crystalline end product is then filtered and dried.

In a further aspect the present invention concerns the compound (I-a) predominantly in Form A. The invention in particular concerns compound (I-a) occurring as a polymorph mixture, which predominantly contains Form A. More in particular the invention concerns compound (I-a), occurring as polymorph mixture containing at least 90 % or more of form A, further in particular 95 % or more of Form A, still further in particular 99 % or more of Form A.

Hence, recrystallization of the compound of formula (I-a) as described above yields a novel crystalline form of (I-a), herein referred to as'Form A'.

Compound (I-a) in Form A has a particular crystalline form, i. e. the monoclinic crystalline form.

One crystalline form of compound (I-a) is referred to as'form B'and is prepared by recrystallisation of compound (I-a) from a suitable solvent. The temperature in this recrystallisation procedure is brought above 60 °C, in particular above 70 °C. Suitable solvents are those wherein the compound of formula (I-a) dissolves at higher temperature and is relatively poorly soluble at lower temperature, e. g. at a temperature lower than 20 °C, or lower than 10 °C, or even lower than 0 °C, or-10 °C. Suitable solvents are the lower alkanols, e. g. the C3 4alkanols and in particular propanol (n- propanol or 2-propanol). Other suitable solvents are esters such as ethyl acetate or a similar solvent, or mixtures thereof with lower boiling halogenated hydrocarbons such as trichloromethane or dichloromethane, which is preferred. In this instance, preferably, the starting material is first dissolved in the ethyl acetate after which the halogenated hydrocarbon is added. The volume of halogenated hydrocarbon that is used is equal to about five times (v/v) relative to the volume of ethyl acetate, preferably the volume ratio is in the range of about 1: 2 to about 1: 5, e. g. it can be about 1: 3 (ethylacetate : halogenated hydrocarbon). Still further suitable solvents are polyols, in particular the glycols such as ethylene glycol, which is preferred, or propylene glycol, butylene glycol and the like. Water can be added, in particular where polyols are used as a solvent. If water is added, it may be acidified with a suitable strong acid such as hydrochloric acid to low pH, e. g. a pH which is in the range of pH 2-5, e. g. a pH which is about pH 3.

Water can be added in various quantities. For example where ethylene glycol or similar glycols are used, the volume ratios of glycol to added water are in the range of 1 : 1 to about 1 : 8, or 1: 2 to 1: 5, e. g. about 1: 4 (glycol: water, v/v).

In one type of embodiment, the compound (I-a) is dissolved by heating or refluxing in 2-propanol, ethyl acetate or a mixture of ethylacetate/dicloromethane, more preferably a 1: 3 mixture of ethylacetate/dichloromethane. Subsequently the solution is allowed to cool whereupon the desired product crystallizes.

This procedure can also be used to convert form A into form B, i. e. by replacing the compound (I-a) by form A in the above procedure.

Form B can also obtained in a highly pure form by heating form A to 130°C over a period of 60 min (DSC experiment) as triclinic crystals.

In a further aspect the present invention concerns the compound (I-a) predominantly in Form B. The invention in particular concerns compound (I-a) occurring as a polymorph mixture, which predominantly contains Form B. More in particular the invention concerns compound (I-a) occurring as polymorph mixture containing at least 90 % or more of form B, further in particular 95 % or more of Form B, still further in particular 99 % or more of form B.

The novel crystalline forms of the compound of formula (I-a) may be characterized by their respective X-ray powder diffraction patterns utilizing appropriate powder diffractometers, in particular using the methodology as outlined in the Examples.

In a further aspect, this invention provides a process for preparing form A of the compound of formula (I-a), or the compound of formula (I-a) predominantly in form A, said process comprising dissolving the compound of formula (I-a) in a suitable solvent, heating the solvent to a temperature which is lower than about 60 °C and higher than about 50 °C, and subsequently allowing to cool said solution. Suitable solvents are alcohols, in particular Cl 4 alkanols, preferably methanol. In a particular execution of this process, the heated solution is allowed to cool until the first crystals appear, in

particular the solution is allowed to cool to about 50 °C allowing the appearance of the first crystals, and subsequently allowed to cool further, in particular to room temperature.

In another aspect, this invention provides a process for preparing form B of the compound of formula (I-a), or the compound of formula (I-a) predominantly in form B, said process comprising recrystallisation of compound (I-a) from a suitable solvent at a temperature of 60 °C or higher, in particular of 70 °C or higher. Suitable solvents are, for example, the lower alkanols, e. g. the C3 4alkanols and in particular propanol. Other suitable solvents are ethyl acetate or mixtures thereof with lower boiling halogenated hydrocarbons such as dichloromethane.

The following Examples describe the invention in greater detail and are intended to illustrate the invention, but not to limit it.

Examples Preparation of - (+)-2- (2-chlorophenyl)-2-hydroxy-ethyl carbamate (compound (I-a)) Example 1 (S)-(+)-2-Chloromandelic acid methyl ester (Intermediate 1) (5)-(+)-2-Chloromandelic acid (100.0 g, 535.9 mmol) is dissolved at rt in methanol (553.0 g). After cooling to 10 5°C, hydrogen chloride gas (55.3 g) is conducted over the solution for 30 min holding the temperature below 25 5°C. The course of this reaction and the following reactions is followed by HPLC. Trimethyl orthoformate (62.6 g, 589.5 mmol) is added at 205°C to the colorless to light yellow solution which is stirred for 30 min at the same temperature. Thereafter the solvent and the hydrogen chloride gas is removed as far as possible in vacuo (40 5°C, 40 10 mbar). The oily

residue is diluted with toluene (130 g) and the solvent is removed again as far as possible in vacuo. Toluene (261 g) is added and the solution is cooled to 15 5°C.

Example 2 2-Methoxy-l-propyl derivatized (S)-(+ !-2-Chloromandelic acid methyl ester (Intermediate 2) Hydrogen chloride gas (0.55 g, 15 mmol) is conducted over the solution (pH-value drops from 3 to 1-2). In a second flask, 2-methoxy-propene (78.0 g, 1081.7 mmol) is dissolved in toluene (120 g) at 20 5°C and the above prepared solution of Intermediate 1 is added at a temperature range of 255°C (ca. 30 min). After the addition is complete, the mixture is stirred for 30 min. Triethylamine (14.0 g, 138.3 mmol) is added to the colorless to light yellow solution, it is stirred at rt for 5 min and diluted with toluene (402 g) (pH > 8, if not, addition of triethylamine). The mixture is washed with water (1 x 150 g), aq. sodium hydrogencarbonate solution (5%, 1 x 150 g), and aq. sat. sodium chloride solution (1 x 150 g). Drying with sodium sulfate (ca. 65 g), filtration, and removal of ca. 86 g toluene in vacuo leads to Intermediate 2.

Example 3 2- (2-Chlorophenyl)-2- (2- (2-methoxv) propyl)-ethanol (Intermediate 3) At first VenpureTM ERS B (13.0 g) and secondly Venpure ERS A (13.0 g) is added and the mixture is heated within 45 min to 855°C. The appearance of the solution turns from clear to slightly cloudy. VenpureTM ERS C (73.9 g, ca. 1239.4 mmol) is dropped into the solution in such a way that the temperature is 95 ~5°C (ca. 45 min, delay of the start of the exothermic reaction is possible). The reaction is finished 15 min after the end of the dropping which is also indicated by an additional milky to gray (from zinc) appearance in the mixture. If not, an additional 7.0 g of each VenpureTM ERS B and VenpureTM ERS A are added directly to the reaction mixture and the whole is heated until the conversion is complete. The solution

is cooled to 15 5°C and methanol (30 g) is added (hydrogen evolution). Aqueous sodium hydroxide solution (30%, 238.0 g) is added dropwise while holding the temperature below 20°C (ca. 30 min, above 25°C, a violent foaming is observed). After the addition is finished the two phase mixture is heated for 1 h to 50 5°C, and the previously formed precipitate dissolves now. The phases are separated after cooling to rt and the colorless organic phase is washed with water (1 x 200 g) and with aq. sat. sodium chloride solution (1 x 200 g). Drying with sodium sulfate (ca. 65 g), filtration, and removal of ca. 180 g solvent in vacuo gives a solution of Intermediate 3.

Example 4 2- (2-chlorophenvl)-2- (2- (2-methoxv) propvl)-ethylcarbamate (Intermediate 5) To the solution obtained in example 3, a slurry of 1, 1'-carbonyl-diimidazole (103.8 g, 641.4 mmol) in toluene (180 g) is added within 30 min. at a temperature in the range of 255°C. The conversion to l-imodazolyl-l'- [2- (2-chlorophenyl) -2- [2- (2- methoxypropyl]-ethoxy carbonyl (Intermediate 4) is then complete.

Toluene (200 g) and aq. ammonium hydroxide solution (25%, 364 g) are added. After 3 h vigorous stirring at rt, the phases are separated and the organic phase containing Intermediate 5 is washed with water (1 x 200 g) and with aqueous saturated sodium chloride solution (1 x 200 g).

Example 5 Preparation of Compound (I-a) To the organic phase containing Intermediate 5, prepared as described above, is added water (160 g) and conc. aq. hydrochloric acid (39 g) generating a pH-value <1. 0.

Compound (I-a) starts precipitating while stirring after 5 min at rt. After 4 h, the product is filtered off, the filter cake is washed with water (3 x 75 g) and with toluene (3 x 44 g). 96.9 g compound (I-a) (purity 99.8%, assay 99.0% determined by HPLC, ee

>99.9% determined by chiral HPLC, 444.8 mmol, overall yield 83.0%) after drying (505°C, 4010 mbar).

Example 6 Preparation of Form A of Compound (I-a) This material of the previous example is suspended in methanol (115 g) and after heating to reflux, the formed solution is hot filtered, cooled to rt, and stirred for 15-20 h at this temperature. Water (577 g) containing aq. conc. hydrochloride acid (ca. 13 mg, pH-value of the solution is 3. 7i0. 2) is added. The mixture is cooled to 55°C, stirred for 2 h at the same temperature, and then filtered. The filter cake is washed with water (3x 30 g). After drying (505°C, 5010 mbar), 93.0 g of Form A of compound (1-a (purity 100%, assay 99.7%, ee >99.9%, 430.0 mmol, overall yield 80.2%) is obtained as colorless needles.

Example 7 Determination of polymorphic form by powder X-ray diffractometry Sample preparation About 0.5 to 1 g of sample is gently pressed into a powder sample holder in order to get a well defined, smooth surface.

Instrument A computer controlled powder diffractometer system APD1700 (Philips) with an automated divergence slit and secondary monochromator or equivalent equipment is used.

Recording conditions

Copper radiation: Kal = 0.15406 and Ka2 = 0.15444 nm Voltage: 40 kV Current: 30 mA Divergence slit: automated Receiving slit: 0. 1° Graphite secondary monochromator for Cu-Ki Xe proportional counter Counting starts at 1. 5° 29 and proceeds in steps of 0. 02° 26 to reach 40° 20. The counting time per interval is 3 sec and the total recording time is 2 h 50 min.

Form A of the compound of formula (I-a) may be characterized by its X-ray diffraction pattern, which comprises the major peaks as listed in the Table 1 in the Examples.

TABLE 1. FORM A POWDER X-RAY DIFFRACTION PEAKS Form B of the compound of formula (II) may be characterized by its X-ray diffraction pattern, which comprises the major peaks as listed in Table 2.

Form A Angle d value Intensity 2-Theta ° Angstrom Cps % 9.217 9.58681 4610 100.0 10.506 8.41395 108 2.3 14.954 5.91952 986 21.4 17.375 5.09990 1501 32.6 18.435 4.80892 3287 71.3 20.028 4. 42979 884 19.2 20.720 4.28343 286 6.2 21.045 4.21801 2535 55.0 22.205 4.00026 80.1 1.7 23.257 3.82165 1248 27.1

24.954 3.56544 494 10.7 25.715 3.46166 1776 38.5 26.093 3.41233 684 14. 8 27.379 3.25489 3953 85.8 27.689 3.21908 954 20.7 29.339 3.04172 163 3.5 30.134 2.96333 517 11.2 31.480 2.83961 129 2.8 31.780 2.81347 310 6.7 32.139 2.78287 113 2.4 32. 880 2.72180 318 6.9 33.097 2.70446 337 7.3 34.664 2.58570 479 10.4 35.170 2.54967 972 21.1 35.500 2.52667 464 10.1 35.995 2.49305 109 2.4 36.700 2.44679 250 5.4 36.958 2.43029 374 8.1 37.314 2.40791 1034 22.4 38.349 2.34527 408 8.9 39.222 2.29508 161 3.5 39.683 2.26945 310 6.7 Example 8 Preparation of Form B of Compound (I-a) 5.0 g (19.0 mmol) raw RWJ-333369 (polymorph A) is dissolved in 4.75 g 2-propanol by heating to reflux. This solution is cooled to room temperature within 30 min whereby the substance crystallizes. After additional stirring at 4°C for 1 h, the product

is filtered off and dried at 80°C and 20 mbar for 8h. Yield: 4.0 g (15.2 mmol, 80%) polymorphic form B.

2-Theta d-value Intens. Rel. Int.

9.13 9.686 486.0 0.324 10.38 8.522 198.0 0.132 12.81 6.910 334.0 0.223 15.04 5.890 507.0 0.338 15.92 5.567 153.0 0.102 17.32 5.120 594.0 0.396 18.31 4.845 694.0 0.463 18.58 4.775 282.0 0.188 19.37 4.582 239.0 0.159 20.04 4.431 326.0 0.217 20.81 4.268 864.0 0.576 21.72 4.092 324.0 0.216 22.15 4.013 1500.0 1.000 23.25 3.826 661.0 0.441 24.94 3.570 416.0 0.277 25.64 3.474 516.0 0.344 27.20 3.278 1044.0 0.696 27.59 3.233 506.0 0.337 28.23 3.161 216.0 0.144 28.56 3.125 221.0 0.147 29.44 3.034 208.0 0.139 30.34 2.946 328.0 0.219 30.83 2.900 314.0 0.209 31.77 2.816 259.0 0.173 32.13 2.786 200.0 0.133 32.68 2.740 335.0 0.223 33.04 2.711 276.0 0.184

34.30 2.614 207.0 0.138 34.81 2.577 621.0 0.414 35.29 2.543 244.0 0.163 35.91 2.501 243.0 0.162 36.36 2.471 189.0 0.126 37.08 2.424 412.0 0.275 37.66 2.388 349.0 0.233 38.55 2.335 431.0 0.287 39.09 2.304 321.0 0.214