WO2010150946A1

WO2010150946A1 - Method for preparation of carbamic acid (r)-1-aryl-2-tetrazolyl-ethyl ester

Info

Publication number: WO2010150946A1
Application number: PCT/KR2009/005906
Authority: WO
Inventors: Sang Chul Lim; Moo Yong Uhm; Nahm Ryune Cho; Dae Won Lee; Ju Young Lee; Hui Ho Kim; Dong Ho Lee
Original assignee: SK Holdings Co Ltd
Current assignee: SK Inc
Priority date: 2009-06-22
Filing date: 2009-10-14
Publication date: 2010-12-29
Anticipated expiration: 2011-12-22
Also published as: EP2445890A1; MX2011013982A; CN102803233A; CN102803233B; RU2012102051A; EP2445890A4; BRPI0924997A2; KR20100137389A; IL216786A; IL216786A0; RU2508290C2; BRPI0924997B1; PL2445890T3; CA2765566A1; US20100323410A1; JP5683580B2; ES2541590T3; EP2445890B1; CA2765566C; AU2009348523B2

Abstract

Disclosed is a method for the preparation of carbamic acid (R)-1-aryl-2-tetrazolyl-ethyl ester, comprising the asymmetric reduction of arylketone and the carbamation of alcohol.

Description

METHOD FOR PREPARATION OF CARBAMIC ACID (R)-1-ARYL-2-TETRAZOLYL-ETHYL ESTER

The present invention relates to a method for the preparation of carbamic acid (R)-1-aryl-2-tetrazolyl-ethyl ester. More particularly, the present invention relates to a method for preparing carbamic acid (R)-1-aryl-2-tetrazolyl-ethyl ester, comprising the asymmetric reduction of an arylketone.

As disclosed in U. S. Patent Application Publication No. 2006/0258718 A1, carbamic acid (R)-1-aryl-2-tetrazolyl-ethyl esters (hereinafter referred to as "the carbamate compounds") with anticonvulsant activity are useful in the treatment of disorders of the central nervous system, especially including anxiety, depression, convulsion, epilepsy, migraines, bipolar disorder, drug abuse, smoking, ADHD, obesity, sleep disorders, neuropathic pain, strokes, cognitive impairment, neurodegeneration, strokes and muscle spasms.

Depending on the position of N in the tetrazole moiety thereof, the carbamate compounds are divided into two positional isomers: tetrazole-1-yl (hereinafter referred to as "1N tetrazole") and treatzole-2-yl (hereinafter referred to as "2N tetrazole"). The introduction of tetrazole for the preparation of the carbamate compounds results in a 1:1 mixture of the two positional isomers which are required to be individually isolated for pharmaceutical use.

Having chirality, the carbamate compounds must be in high optical purity as well as chemical purity as they are used as medications.

In this regard, U. S. Patent Application Publication No. 2006/0258718 A1 uses the pure enantiomer (R)-aryl-oxirane as a starting material which is converted into an alcohol intermediate through a ring-opening reaction by tetrazole in the presence of a suitable base in a solvent, followed by introducing a carbamoyl group into the alcohol intermediate. For isolation and purification of the 1N and 2N positional isomers thus produced, column chromatography is set after the formation of an alcohol intermediate or carbamate.

For use in the preparation, (R)-2-aryl-oxirane may be synthesized from an optically active material, such as substituted (R)-mandelic acid derivative, via various routes or obtained by asymmetric reduction-ring formation reaction of α-halo arylketone or by separation of racemic 2-aryl-oxirane mixture into its individual enantiomers. As such, (R)-2-aryl-oxirane is an expensive compound.

In addition, the ring-opening reaction of (R)-2-aryl-oxirane with tetrazole is performed at relatively high temperatures because of the low nucleophilicity of the tetrazole. However, the ring opening reaction includes highly likely risk of a runaway reaction because tetrazoles start to spontaneously degrade at 110 ~ 120℃.

In terms of a selection of reaction, as there are two reaction sites in each (R)-2-aryl-oxirane and tetrazole, the ring-opening reaction therebetween affords the substitution of 1N- or 2N-tetrazole at the benzyl or terminal position, resulting in a mixture of a total of 4 positional isomers. Therefore, individual positional isomers are low in production yield and difficult to isolate and purify.

Accordingly, the present invention has been made keeping in mind the above problems occurring in the prior art, and an object of the present invention is to provide a novel method for preparing novel (R)-1-aryl-2-tetrazolyl-ethyl ester.

In order to accomplish the above object, the present invention provides a method for preparing carbamic acid (R)-1-aryl-2-tetrazolyl ethyl ester, represented by Chemistry Figure 1, comprising: subjecting an arylketone, represented by Chemistry Figure 2, to (R)-selective asymmetric reduction to form an alcohol compound of (R)-configuration, represented by Chemistry Figure 5; and carbamating said alcohol:

ChemistryFigure 1

ChemistryFigure 2

ChemistryFigure 5

wherein,

R₁ and R₂ are independently selected from a group consisting of hydrogen, halogen, perfluoroalkyl, alkyl of 1 to 8 carbon atoms, thioalkoxy of 1 to 8 carbon atoms, and alkoxy of 1 to 8 carbon atoms; and

one of A₁ and A₂ is CH with the other being N.

An economical advantage is given to the synthesis of the arylketone of Chemistry Figure 2 from the compounds represented by Chemistry Figures 8 and 9 because they are commercially available, cheap compounds. In addition, the substitution reaction can be carried out in relatively mild conditions, compared to the ring-opening reaction between (R)-2-aryl-oxirane and tetrazole. The method according to the present invention is therefore certain of process safety although employing potentially explosive tetrazole, and ensures high production yield and easy purification, with the production of no unnecessary positional isomers at benzyl positions.

In accordance with an embodiment of the present invention, a method comprising (R)-selective asymmetric reduction of an arylketone represented by the following Chemistry Figure 2 and the carbamation of an alcohol compound represented by the following Chemistry Figure 5 is provided for the preparation of carbamic acid (R)-1-aryl-2-tetrazolyl-ethyl ester, represented by the following Chemistry Figure 1.

[Chemistry Figure 1]

[Chemistry Figure 2]

[Chemistry Figure 5]

wherein,

one of A₁ and A₂ is CH with the other being N.

The arylketone of Chemistry Figure 2, useful as a starting material in the preparation method of the present invention, may be synthesized by, for example, a substitution reaction between the arylketone of Chemistry Figure 8 and the tetrazole of Chemistry Figure 9:

ChemistryFigure 8

ChemistryFigure 9

wherein,

R₁ and R₂ are as defined above; and

X is a leaving group such as a halide or sulfonate.

The arylketone represented by Chemistry Figure 2 which can be synthesized by the substitution reaction with tetrazole may be in a mixture of positional isomers including 1N arylketone of the following Chemistry Figure 3 and 2N arylketone of the following Chemistry Figure 4, which can be isolated and purified through commercially available crystallization.

ChemistryFigure 3

ChemistryFigure 4

The crystallization useful in the present invention may comprise adding a solubilizing agent to the product of the substitution reaction, that is, a mixture of the positional isomers, and then adding a precipitating agent. Optionally, the crystallization may further comprise, after the precipitation, filtrating the precipitate, concentrating the filtrate and adding an additional precipitating agent.

Illustrative, non-limiting examples of the solubilizing agent include acetone, acetonitrile, tetrahydrofuran, ethylacetate, dichloromethane, chloroform, 1,4-dioxane, and lower alcohols of 1 to 4 carbon atoms, and a combination thereof. The solubilizing agent may be used in an amount of from 0 to 20 ml (v/w) based on the weight (g) of the mixture of the positional isomers. As used herein, the addition of the solubilizing agent in an amount of zero ml (v/w) is intended to mean immediately adding the subsequent additive without dilution of the filtrate.

Examples of the precipitating agent include water, C1-C4 lower alcohol, diethylether, pentane, hexane, cyclohexane, heptane and a combination thereof, but are not limited thereto. The precipitating agent may be slowly added in an amount of from zero to 40 ml (v/w) based on the weight (g) of the mixture of positional isomers. As used herein, the addition of the precipitating agent in an amount of zero ml is intended to mean leaving or cooling to yield precipitates without the addition of the precipitating agent.

The filtration of the precipitates thus obtained by the addition of the precipitating agent yields the 1N arylketone of Chemistry Figure 3 as a crystal with high purity.

On the other hand, the filtrate thus obtained after the filtration step may be concentrated to increase the ratio of the precipitating agent to the solubilizing agent, thereby yielding the 2N arylketone of Chemistry Figure 4 with high purity. Concentration ratio of the filtrate can be suitably determined by those of ordinary skill in the art. For example, concentration is carried until the solvent is totally removed off, then the solubilizing agent and the precipitating agent are added as mentioned above.

Unlike column chromatography, this crystallization may be commercially used without much difficulty.

(R)-Selective asymmetric reduction allows for the conversion of the arylketone of Chemistry Figure 2 into the alcohol compound with (R)-configuration, represented by the following Chemistry Figure 5.

[Chemistry Figure 2]

[Chemistry Figure 5]

wherein,

R₁ and R₂ are independently selected from a group consisting of hydrogen, halogen, perfluoroalkyl, an alkyl of 1 to 8 carbon atoms, a thioalkoxy of 1 to 8 carbon atoms, and alkoxy of 1 to 8 carbon atoms; and

one of A₁ and A₂ is CH with the other being N.

The (R)-selective asymmetric reduction can be achieved, for example, biologically or chemically.

In the method for preparing carbamic acid (R)-1-aryl-2-tetrazolyl-ethyl ester according to an embodiment of the present invention, the arylketone compound of Chemistry Figure 2 is converted into an alcohol compound with (R)-configuration of optically high purity by biological asymmetric reduction.

The biological asymmetric reduction can be achieved in a buffer containing a microbial strain capable of producing oxidoreductase, the arylketone compound of Chemistry Figure 2 and a cosubstrate at an appropriate temperature. Examples of the microbial strain capable of producing oxidoreductase include yeast of the Candida genus, such as Candida parapsilosis or Candida rugosa; yeast of the Pichia genus, such as Pichia anomala or Pichia jadinii; yeast of the Saccharomyces genus, such as Baker's yeast, Saccharomyces cerevisiae or Saccharomyces pastorianus; other yeast such as Rhodotorula mucilaginosa or Trigonopsis variabilis; bacteria, such as Klebsiella pneumoniae, Enterobacter cloacae, Erwinia herbicola, Micrococcus luteus, Bacillus stearothermophilus, Rhodococcus erythropolis or Rhodococcus rhodochrous; fungi, such as Mucor racemosus or Geotrichum candidum, etc.

The microbial strain capable of producing oxidoreductase may be used in an amount of from about 0.1 to 10 g per gram of the arylketone of Chemistry Figure 2.

To enhance the rate of the biological asymmetric reduction, an additional coenzyme such as nicotineamide adenine dinucleotide phosphate (NADP) or nicotineamide adenine dinucleotide (NAD) may be added to the buffer with a use amount from about 0.1 to 1 mg per gram of the arylketone of Chemistry Figure 2.

The coenzyme, NADP or NAD may be converted to its reduced form, NADPH or NADH, respectively with the aid of the oxidoreductase and/or a cosubstrate.

Examples of the cosubstrate include saccharides such a glucose, glycerol or sucrose; and alcohols such as methanol, ethanol, 1-propanol, isopropanol, 1-butanol, 2-butanol, 2-pentanol, 2-methylpentanol, 2-hexanol, 2-heptanol, 2-octanol, cyclopentanol, cyclohexanol, 2-methyl 2-butanol, etc. Among the alcohols mentioned beforehand, methanol, 1-propanol, 1-butanol and 2-methyl 2-butanol are preferable.

The buffer useful in the biological asymmetric reduction may be PBS (phosphate buffered saline) or a solution of sodium phosphate, potassium phosphate or triethanolamine in water, for example, at a pH of 6 to 8.

The biological asymmetric reduction may be carried out at from 10 to 45℃.

In addition to being economical and environment-friendly, the biological selective reduction allows for very high enantioselectivity. Thus, an alcohol compound with an (R)-configuration of high optical purity can be obtained in the presence of the enzyme under the above-mentioned reaction conditions.

In the method for preparing carbamic acid (R)-1-aryl-2-tetrazolyl-ethyl ester according to another embodiment of the present invention, the arylketone compound of Chemistry Figure 2 is chemically converted into an alcohol compound with (R)-configuration of high optical purity under asymmetric conditions.

Chemical asymmetric reduction may be accomplished, for example, with a chiral borane reductant at an appropriate temperature in an organic solvent, or by asymmetric catalytic hydrogenation or asymmetric catalytic transfer hydrogenation.

As concerns the use of a chiral borane reductant, 1 to 4 equivalents of sodium (-)-B-chlorodiisopinochampheylborane (hereinafter referred to as "(-)-DIP-Cl") or (R)-2-methyl-CBS-oxazaborolidine/borane (hereinafter referred to as "(R)-CBS/BH₃") are added to a solution of the arylketone compound of Chemistry Figure 2 in an organic solvent such as diethylether, tetrahydrofuran, 1,4-dioxane, acetonitrile, dichloromethane, chloroform or a mixture thereof, and the reaction may be conducted at about -10 to about 60℃.

The asymmetric catalytic hydrogenation may be conducted as follows: the 0.0004 to 0.2 equivalents of an inorganic base may be added to the solution with 0.0002 to 0.1 equivalents of (R)-bisphosphono-ruthenium (II)-(R,R)-chiral diamine complex catalyst dissolved in organic solvent such as isopropanol, methanol, ethanol or t-butylalcohol. The arylketone compound of Chemistry Figure 2 may be added and the resultant solution may hold at about -10 to about 60℃ under hydrogen pressure of 1 to 20 atm. A non-limiting example of the catalyst useful in the asymmetric catalytic hydrogenation is dichloro[(R)-(+)-2,2'-bis(diphenylphosphono)1,1'-binaphthyl][(1R,2R)-(+)-1,2-diphenylethylenediamine]ruthenium(II) represented by the following Chemistry Figure 10.

ChemistryFigure 10

Turning to the asymmetric catalytic transfer hydrogenation, it may be carried out by adding 0.001 ~ 0.1 equivalents of [S,S]-monosulfonatediamine-M(II) arene complex catalyst (wherein M is ruthenium or rhodium) to a solution of the arylketone compound of Chemistry Figure 2 in 5:2 formic acid-triethylamine azeotrope or isopropanol at about -10 to 60℃. A non-limiting example of catalyst useful for the asymmetric catalytic transfer hydrogenation may be chloro｛[(1S,2S)-(+)-amino-1,2-diphenylethyl](4-toluenesulfonyl)amido｝(p-cymene)ruthenium(II), represented by the following Chemistry Figure 11.

ChemistryFigure 11

The alcohol compound obtained through the asymmetric reduction may exist as a positional isomer mixture of 1N alcohol of Chemistry Figure 6 and 2N alcohol of Chemistry Figure 7 that can be isolated and purified into individual positional isomers of high purity by crystallization:

ChemistryFigure 6

ChemistryFigure 7

The crystallization may comprise adding a solubilizing agent to the positional isomer mixture resulting from the asymmetric reduction; and adding a precipitating agent, and optionally filtering the precipitate; and concentrating the filtrate and adding an additional precipitating agent.

Examples of the solubilizing agent useful in the crystallization include acetone, acetonitrile, tetrahydrofuran, ethylacetate, dichloromethane, chloroform, 1,4-dioxane, lower alcohol of 1 to 4 carbon atoms, and a mixture thereof, but are not limited thereto. The solubilizing agent may be added in an amount of zero to 20 ml (v/w) based on the weight (g) of the positional isomer mixture.

Non-limiting examples of the precipitating agent include water, a lower alcohol of 1 to 4 carbon atoms, diethylether, pentane, hexane, cyclohexane, heptane, and a mixture thereof. The precipitating agent may be slowly added in an amount of from zero to 40 ml (v/w) based on the weight (g) of the positional isomer mixture.

Following the addition of the precipitating agent, filtration may yield 1N alcohol (6) as a precipitate of high purity.

Furthermore, 2N alcohol (7) can be obtained as a crystal form of very high purity by concentrating the filtrate and increasing the ratio of the precipitating agent to the solubilizing agent.

These crystallization steps may be omitted when the positional isomers of arylketone of Chemistry Figure 2 are already isolated and purified.

The introduction of a carbomoyl moiety into the alcohol compound with (R)-configuration of Chemistry Figure 5 leads to carbamate with (R)-configuration, represented by Chemistry Figure 1:

[Chemistry Figure 5]

[Chemistry Figure 1]

wherein,

R₁ and R₂ are independently selected from a group consisting of hydrogen, halogen, perfluoroalkyl, an alkyl of 1 to 8 carbon atoms, a thioalkoxy of 1 to 8 carbon atoms, and an alkoxy of 1 to 8 carbon atoms; and

one of A₁ and A₂ is CH with the other being N.

In the carbamation step, for example, inorganic cyanate-organic acid, isocyanate-water, or carbonyl compound-ammonia may be employed to introduce a carbamoyl moiety.

For the carbamation with inorganic cyanate-organic acid, the alcohol compound with (R)-configuration of Chemistry Figure 5 is dissolved in an organic solvent, for example, diethylether, tetrahydrofuran, 1,4-dioxane, acetonitrile, dichloromethane, chloroform or a mixture thereof, and mixed with 1 to 4 equivalents of inorganic cyanate such as sodium cyanate and organic acid, such as methane sulfonic acid or acetic acid, followed by reacting at about -10 to 70℃.

With regard to use of the isocyanate-water, 1 to 4 equivalents of isocyanate, for example, chlorosulfonic isocyanate, trichloroacetyl isocyanate, trimethylsilyl isocyanate, are added to a solution of the alcohol compound with (R)-configuration of Chemistry Figure 5 in an organic solvent, for example, diethylether, tetrahydrofuran, 1,4-dioxane, acetonitrile, dichloromethane, chloroform or a mixture thereof, and reacted at about -50 to 40℃. Subsequently, without purification, 1 to 20 equivalents of water were added to induce hydrolysis.

With regard to use of the carbonyl compound-ammonia,

1 to 4 equivalents of a carbonyl compound, for example, 1,1'-carbonyldiimidazole, carbamoly chloride, disuccinyl carbonate, phosgene, triphosgene, or chloroformate, are added to a solution of the alcohol compound with (R)-configuration of Chemistry Figure 5 in an organic solvent, for example, diethylether, tetrahydrofuran, 1,4-dioxane, acetonitrile, dichloromethane, chloroform or a mixture thereof, and reacted at about -10 to 70℃, followed by adding 1 to 10 equivalents of ammonia without purification.

After the carbamation, the carbamate compound of Chemistry Figure 1 thus obtained may be purified to higher optical and chemical purity through the following crystallization. The crystallization comprises adding a solubilizing agent to the product of the carbamation; and then adding a precipitating agent, and optionally filtering the precipitate and adding an additional precipitating agent. For pharmaceutical use, it is preferable that there is always a final purification of the carbamated product before use, but that there can be a crystallization step earlier in the process.

Non-limiting examples of the solubilizing agent include acetone, acetonitrile, tetrahydrofuran, ethylacetate, dichloromethane, chloroform, 1,4-dioxane, lower alcohol of 1 to 4 carbon atoms, and a mixture thereof. Based on the weight (g) of the reaction product, the solubilizing agent may be used in an amount of from zero to 20 ml (v/w).

Non-limiting examples of the precipitating agent include water, lower alcohols of 1 to 4 carbon atoms, diethylether, pentane, hexane, cyclohexane, heptane and a mixture thereof. Based on the weight (g) of the reaction product, the precipitating agent may be slowly added in an amount of from zero to 40 ml (v/w). Comprising biological or chemical asymmetric reduction, the method of the present invention can provide optically high pure carbamate compounds. In addition, the mild reaction conditions which the method of the present invention requires ensure process safety. Furthermore, the crystallization step applicable to large-scale production before or after the asymmetric reduction or after the carbamation results in a higher chemical purity of the carbamate compounds.

As demonstrated in the following examples, the carbamate compounds prepared according to the present invention are very useful in the treatment of CNS disorders such as convulsion.

A better understanding of the present invention may be obtained through the following examples which are set forth to illustrate, but are not to be construed as limiting the present invention.

EXAMPLES

Preparation of Tetrazole Arylketones

Preparation Example 1: Preparation of 1-(2-chlorophenyl)-2-(1,2,3,4-tetrazol-1-yl)ethan-1-one

To a suspension of 2-bromo-2'-chloroacetophenone (228.3 g, 0.978 mol) and potassium carbonate (161.6 g, 1.170 mol) in acetonitrile (2000 mL) was added a 35 w/w% 1H-tetrazole dimethylformamide solution (215.1 g, 1.080 mol) at room temperature. These reactants were stirred for 2 h at 45℃ and distilled under reduced pressure to remove about 1500 mL of the solvent. The concentrate was diluted in ethylacetate (2000 mL) and washed with 10% brine (3 x 2000 mL). The organic layer thus separated was distilled under reduced pressure to afford 216.4 g of an oily solid residue. To a solution of the solid residue in ethylacetate (432 mL) was slowly added heptane (600 mL). The precipitate thus formed was filtered at room temperature and washed to yield 90.1 g (0.405 mol) of 1-(2-chlorophenyl)-2-(1,2,3,4-tetrazol-1-yl)ethan-1-one (hereinafter referred to as "1N ketone").

¹H-NMR(CDCl₃)d8.87(s, 1H), d7.77(d, 1H), d7.39-7.62(m, 3H), d5.98(s, 2H)

Preparation Example 2: Preparation of 1-(2-chlorophenyl)-2-(1,2,3,4-tetrazol-2-yl)ethan-1-one

After the filtration of Preparation Example 1, the filtrate was concentrated and dissolved in isopropanol (100 mL), and to which heptane (400 mL) was then added to complete the crystallization. Filtering and washing at 5℃ afforded 1-(2-chlorophenyl)-2-(1,2,3,4-tetrazol-2-yl)ethan-1-one (hereinafter referred to as "2N ketone") as a solid. 94.7 g (0.425 mol).

¹H-NMR(CDCl₃) d8.62(s, 1H), d7.72(d, 1H), d7.35-7.55(m, 3H), d6.17(s, 2H)

Preparation of Alcohol Compound of (R)-Configuration by Biological Asymmetric Reduction

Suitable for use in the biological asymmetric reduction is a strain expressing oxidoreductase. Like baker s yeast (Jenico), a strain commercially available in a freeze-dried form may be weighed properly for the reaction. As like other micorbial strans, the strain stored in a deep freezer (Revco) may be spread on LB plates medium (Bactotrypton: 1%, yeast extract: 0.5%, NaCl: 0.5%, glucose: 0.1%, agar: 1.5%) to form colonies. The one of which is then inoculated into 3 mL of an LB medium in a tube and pre-incubated at 30℃ for 1 day. After completion of the pre-incubation, it was scaled up to 300 mL of LB medium in 1L Erlenmeyer flask, followed by incubation at 30℃ for 2 days. Centrifugation precipitates the strain into a pellet which is quantified for use in the reaction.

Preparation Example 3: Preparation of 1N Alcohol with Rhodotorula mucilaginosa

1-(2-Chlorophenyl)-2-(1,2,3,4-tetrazol-1-yl)ethan-1-one (100mg, 0.449mmol), prepared in Preparation Example 1, was incubated at room temperature for 4 days with nicotinamide adenine dinucleotide (NAD, 0.5 mg) in the presence of Rhodotorula mucilaginosa KCTC7117 (500 mg), a microbial strain producing oxidoreductase, in PBS (10mL, pH7.0) containing 5% (w/v) glycerol, after which extraction with ethylacetate (1 mL) gave an alcohol of R-configuration, that is, (R)-1-(2-chlorophenyl)-2-(1,2,3,4-tetrazol-1-yl)ethan-1-ol (hereinafter referred to as "1N alcohol"). Conversion rates and optical purities of products are listed in Table 1, below. Conversion rates (%), purities (%) and optical purities of products were measured using HPLC and calculated using the following equations.

Conversion Rate (%) = [(Area of Product)/(Area of Reactant + Area of Product)]x100

Purity (%) = (Area of Product)/(Area of All Peaks on HPLC)] x 100

Optical Purity (%) = [(Area of R-Configuration Area of S-Configuration)/(Area of R-Configuration + Area of S-Configuration)] x 100

¹H-NMR(CDCl₃) d8.74(s, 1H), d7.21-7.63(m, 4H), d5.57(m, 1H), d4.90(d, 1H), d4.50(d, 1H), d3.18(d, 1H)

Preparation Example 4: Preparation of 2N Alcohol with Rhodotorula mucilaginosa

The same procedure as in Preparation Example 3 was repeated, with the exception that 1-(2-chlorophenyl)-2-(1,2,3,4-tetrazol-2-yl)ethan-1-one, prepared in Preparation Example 2, was used instead of 1-(2-chlorophenyl)-2-(1,2,3,4-tetrazol-1-yl)ethan-1-one, to afford (R)-1-(2-chlorophenyl)-2-(1,2,3,4-tetrazol-2-yl)ethan-1-ol (hereinafter referred to as "2N alcohol"). The conversion rate and optical purity of the product are given in Table 1, below.

¹H-NMR(CDCl₃) d8.55(s, 1H), d7.28-7.66(m, 4H), d5.73(d, 1H), d4.98(d, 1H), d4.83(d, 1H), d3.38(br, 1H)

Preparation Example 5: Preparation of 1N Alcohol with Trigonopsis variabilis

The same procedure as in Preparation Example 3 was repeated, with the exception that Trigonopsis variabilis KCTC7263 was used as a strain producing an oxidoreductase, instead of Rhodotorula mucilaginosa KCTC7117, to afford 1N alcohol of R-configuration. Its conversion rate and optical purity are given in Table 1, below.

Preparation Example 6: Preparation of 2N Alcohol with Trigonopsis variabilis

The same procedure as in Preparation Example 4 was repeated, with the exception that Trigonopsis variabilis KCTC7263 was used as a strain producing an oxidoreductase, instead of Rhodotorula mucilaginosa KCTC7117, to afford 2N alcohol of R-configuration. Its conversion rate and optical purity are given in Table 1, below.

Table 1

Preparation Examples 7 and 8: Preparation of 1N Alcohol with Yeasts of Candida Genus

The same procedure as in Preparation Example 3 was repeated, with the exception that Candida parapsilosis ATCC20179 or Candida rugosa KCTC7292 was used as a strain producing an oxidoreductase, instead of Rhodotorula mucilaginosa KCTC7117, to afford 1N alcohol of R-configuration. Its conversion rate and optical purity are given in Table 2, below.

Preparation Examples 9 and 10: Preparation of 2N Alcohol with Yeasts of Candida Genus

The same procedure as in Preparation Example 4 was repeated, with the exception that Candida parapsilosis ATCC20179 or Candida rugosa KCTC7292 was used as a strain producing an oxidoreductase, instead of Rhodotorula mucilaginosa KCTC7117, to afford 2N alcohol of R-configuration. Its conversion rate and optical purity are given in Table 2, below.

Table 2

Preparation Examples 11 and 12: Preparation of 1N Alcohol with Yeasts of Pichia Genus

The same procedure as in Preparation Example 3 was repeated, with the exception that Pichia anomala KCTC1206 or Pichia jadinii KCTC7008 was used as a strain producing an oxidoreductase, instead of Rhodotorula mucilaginosa KCTC7117, to afford 1N alcohol of R-configuration. Its conversion rate and optical purity are given in Table 3, below.

Preparation Examples 13 and 14: Preparation of 2N Alcohol with Yeasts of Pichia Genus

The same procedure as in Preparation Example 4 was repeated, with the exception that Pichia anomala KCTC1206 or Pichia jadinii KCTC7008 was used as a strain producing an oxidoreductase, instead of Rhodotorula mucilaginosa KCTC7117, to afford 2N alcohol of R-configuration. Its conversion rate and optical purity are given in Table 3, below.

Table 3

Preparation Examples 15 to 20: Preparation of 1N Alcohol with Yeast of Saccharomyces Genus

The same procedure as in Preparation Example 4 was repeated, with the exception that Baker's yeast, Saccharomyces cerevisiae KCTC7108, Saccharomyces cerevisiae KCTC1205, Saccharomyces cerevisiae KCTC7107, Saccharomyces cerevisiae KCTC1552 or Saccharomyces pastorianus KCTC1218 was used as a strain producing an oxidoreductase, instead of Rhodotorula mucilaginosa KCTC7117, to afford 1N alcohol of R-configuration. Its conversion rate and optical purity are given in Table 4, below.

Preparation Example 21 to 26: Preparation of 2N Alcohol with Yeasts of Saccharomyces Genus

The same procedure as in Preparation Example 4 was repeated, with the exception that Baker's yeast, Saccharomyces cerevisiae KCTC7108, Saccharomyces cerevisiae KCTC1205, Saccharomyces cerevisiae KCTC7107, Saccharomyces cerevisiae KCTC1552 or Saccharomyces pastorianus KCTC1218 was used as a strain producing an oxidoreductase, instead of Rhodotorula mucilaginosa KCTC7117, to afford 2N alcohol of R-configuration. Its conversion rate and optical purity are given in Table 4, below.

Table 4

Preparation Examples 27 to 30: Preparation of 1N Alcohol with Bacteria

The same procedure as in Preparation Example 3 was repeated, with the exception that Klebsiella pneumoniae IFO3319, Bacillus stearothermophilus KCTC1752, Rhodococcus erythropolis KCCM40452 or Rhodococcus rhodochrous ATCC21197 was used as a strain producing an oxidoreductase, instead of Rhodotorula mucilaginosa KCTC7117, to afford 1N alcohol of R-configuration. Their conversion rates and optical purities are given in Table 5, below.

Preparation Examples 31 to 37: Preparation of 2N Alcohol with Bacteria

The same procedure as in Preparation Example 4 was repeated, with the exception that Klebsiella pneumoniae IFO3319, Enterobacter cloacae KCTC2361, Erwinia herbicola KCTC2104, Micrococcus luteus KCTC1071, Bacillus stearothermophilus KCTC1752, Rhodococcus erythropolis KCCM40452 or Rhodococcus rhodochrous ATCC21197 was used as a strain producing an oxidoreductase, instead of Rhodotorula mucilaginosa KCTC7117, to afford 2N alcohol of R-configuration. Their conversion rates and optical purities are given in Table 5, below.

Table 5

Preparation Examples 38 and 39: Preparation of 1N Alcohol with Fungi

The same procedure as in Preparation Example 3 was repeated, with the exception that Mucor racemosus KCTC6119, Geotrichum candidum KCTC6195, Geotrichum candidum IFO5767 or Geotrichum candidum IFO4597 was used as a strain producing an oxidoreductase, instead of Rhodotorula mucilaginosa KCTC7117, to afford 1N alcohol of R-configuration. Their conversion rates and optical purities are given in Table 6, below.

Preparation Examples 40 to 42: Preparation of 2N Alcohol with Fungi

The same procedure as in Preparation Example 4 was repeated, with the exception that Mucor racemosus KCTC6119, Geotrichum candidum KCTC6195, Geotrichum candidum IFO5767 or Geotrichum candidum IFO4597 was used as a strain producing an oxidoreductase, instead of Rhodotorula mucilaginosa KCTC7117, to afford 2N alcohol of R-configuration. Their conversion rates and optical purities are given in Table 6, below.

Table 6

Preparation of Alcohol Compound of (R)-Configuration by Chemical Asymmetric Reduction

Preparation Examples 43 and 44: Preparation of 1N Alcohol with Chiral Borane Reductant

To a solution of 1N ketone (100 mg, 0.449 mmol), prepared in Preparation Example 1, in tetrahydrofuran (1 mL) was added 2 equivalents of a chiral borane reductant, such as (-)-B-chlorodiisopinocampheylborane or (R)-2-methyl-CBS-oxazaborolidine/borane, at 0℃. Stirring at room temperature for 24h was followed by extraction with ethyl acetate (1 mL) to give the results of Table 7, below.

Preparation Examples 45 and 46: Preparation of 2N Alcohol with Chiral Borane Reductant

To a solution of 2N ketone (100 mg, 0.449 mmol), prepared in Preparation Example 2, in tetrahydrofuran (1 mL) was added 2 equivalents of a chiral borane reductant, such as (-)-B-chlorodiisopinocampheylborane or (R)-2-methyl-CBS-oxazaborolidine/borane, at 0℃. Stirring at room temperature for 24h was followed by extraction with ethyl acetate (1 mL) to give the results of Table 7, below.

Table 7

Preparation Examples 47 and 48: Preparation of 1N and 2N Alcohols with Asymmetric Catalytic Transfer Hydrogenation

The 1N ketone prepared in Preparation Example 1 or 2N ketone prepared in Preparation Example 2 (222 mg, 1.0 mmol) was dissolved in a 5:2 formic acid-triethylamine azeotrope (1.4 mL) and subjected to an argon environment. After the solution was cooled to 0℃ in the argon environment, chloro｛[(1S,2S)-(+)-amino-1,2-diphenylethyl](4-toluenesulfonyl)amido｝(p-cymene)ruthenium(II) (2 mg, 0.00 3mmol) of Chemistry Figure 11 was added thereto. Stirring at room temperature for 48 h was followed by extraction with ethyl acetate (2 mL) to give the results of Table 8, below.

Table 8

Preparation of Carbamate

Preparation Example 49: Preparation of Carbamic Acid (R)-1-(2-Chlorophenyl)-2-(tetrazol-1-yl)ethyl ester

To PBS (1000mL, pH 7.0) containing 5%(w/v) glycerol were added baker's yeast (50 g) and 1N ketone (10 g, 44.9 mmol) prepared in preparation example 1, together with nicotineamide adenine dinucleotide (NAD, 1 mg). The resulting reaction suspension was stirred at 30℃ for 4 days and mixed with ethyl acetate (500 mL). After being separated, the organic layer thus formed was washed with 10% brine (3 x 500 mL). To the organic layer was added magnesium sulfate, followed by filtering the resulting suspension. The filtrate was distilled under reduced pressure to afford 8.5 g of a solid residue which was then dissolved at 45℃ in ethyl acetate (10 mL) and cooled to room temperature. Slow addition of heptane (20 mL) led to crystallization. The precipitate thus formed was filtered and washed to give 7.32 g (32.6 mmol) of 1-(2-chlorophenyl)-2-(1,2,3,4-tetrazol-1-yl)ethan-1-ol (optical purity 99.9%). The precipitate was dissolved in dichloromethane (73 mL) to which methanesulfonic acid (5.5 mL, 84.7 mmol) was added at 10℃, followed by the slow addition of sodium cyanate (4.24 g, 65.2 mmol). The reactant mixture was stirred at 10℃ for 12h and washed with 10% brine (3 x 100 mL). The organic layer thus formed was concentrated under reduced pressure and the concentrate was dissolved in isopropanol (14 mL). Heating the solution to 45℃ and cooling to room temperature led to the completion of crystallization. The precipitate thus obtained was filtered and washed to afford 7.84 g (29.3 mmol) of carbamic acid (R)-1-(2-chlorophenyl)-2-(tetrazol-1-yl)ethyl ester (purity >99.0%, optical purity >99.0%).

¹H-NMR(Acetone-d₆) d9.14(s, 1H), d7.31-7.59(m, 4H), 6.42(m, 1H), d6.0-6.75(Br, 2H), d4.90(d, 1H), d5.03(m, 2H)

Preparation Example 50: Preparation of Carbamic Acid (R)-1-(2-Chlorophenyl)-2-(tetrazol-2-yl)ethyl ester

The 2N ketone (15.5 g, 69.6 mmol), prepared in Preparation Example 2, was dissolved in a 5:2 formic acid-triethylamine azeotrope (60 mL) and subjected to an argon environment. To this solution was added chloro｛[(1S,2S)-(+)-amino-1,2-diphenylethyl](4-toluenesulfonyl)amido｝(p-cymene)ruthenium(II) of Chemistry Figure 11 (140 mg, 0.220 mmol), followed by stirring at room temperature for 48 h. The solution was diluted in ethylacetate (200 mL) and washed with 10% brine (3 x 100 mL). The organic layer thus formed was dried over magnesium sulfate and filtered and the filtrate was distilled under reduced pressure to give 14.8 g (65.9 mmol) of 1-(2-chlorophenyl)-2-(1,2,3,4-tetrazol-2-yl)ethan-1-ol (optical purity 87.8%) as an oily residue. To this was added tetrahydrofuran (150 mL). After cooling to -15℃, chlorosulfonyl isocyanate (6.9 mL, 79.2 mmol) was slowly added and stirred at -10℃ for 2 h. The slow addition of water (10 mL) induced termination of the reaction. The resulting solution was concentrated under reduced pressure until about 100 mL of the solvent was removed. The concentrate was diluted in ethyl acetate (200 mL) and washed with 10% brine (3 x 150 mL). The organic layer was concentrated under reduced pressure and the concentrate was dissolved in isopropanol (30 mL) to which heptane (90 mL) was slowly added, leading to the completion of crystallization. The precipitate thus obtained was filtered and washed to afford 15.4 g (57.5 mmol) of carbamic acid (R)-1-(2-chlorophenyl)-2-(tetrazol-2-yl)ethyl ester (purity >99.0%, optical purity>99.0%).

¹H-NMR(Acetone-d₆) d8.74(s, 1H), d7.38-7.54(m, 4H), d6.59(m, 1H), d6.16(Br, 2H), d4.90(d, 1H), d5.09(m, 2H)

As described hitherto, carbamate compounds with high optical and chemical purity can be produced with an economical benefit in accordance with the present invention.

Although the preferred embodiments of the present invention have been disclosed for illustrative purposes, those skilled in the art will appreciate that various modifications, additions and substitutions are possible, without departing from the scope and spirit of the invention as disclosed in the accompanying claims.

Claims

A method for preparing carbamic acid aryl-2-tetrazolyl ethyl ester, represented by Chemistry Figure 1, comprising:

subjecting an arylketone, represented by Chemistry Figure 2, to (R)-selective asymmetric reduction to form an alcohol compound of (R)-configuration, represented by Chemistry Figure 5; and

carbamating said alcohol:

[Chemistry Figure 1]

[Chemistry Figure 2]

[Chemistry Figure 5]

wherein,

R₁ and R₂ are independently selected from a group consisting of hydrogen, halogen, perfluoroalkyl, an alkyl of 1 to 8 carbon atoms, a thioalkoxy of 1 to 8 carbon atoms, and an alkoxy of 1 to 8 carbon atoms; and

one of A₁ and A₂ is CH with the other being N.
The method according to claim 1, wherein the (R)-selective asymmetric reduction is achieved by biological asymmetric reduction or chemical asymmetric reduction.
The method according to claim 2, wherein the biological asymmetric reduction is carried out in a buffer containing the arylketone of Chemistry Figure 2, a microbial strain capable of producing oxidoreductase, and a cosubstrate.
The method according to claim 3, wherein the microbial strain is selected from a group consisting of yeasts of Candida genus including Candida parapsilosis and Candida rugosa; yeasts of Pichia genus including Pichia anomala and Pichia jadinii; yeasts of Saccharomyces genus including Baker's yeast, Saccharomyces cerevisiae and Saccharomyces pastorianus; yeasts including Rhodotorula mucilaginosa and Trigonopsis variabilis; bacteria including Klebsiella pneumoniae, Enterobacter cloacae, Erwinia herbicola, Micrococcus luteus, Bacillus stearothermophilus, Rhodococcus erythropolis and Rhodococcus rhodochrous; fungi including Mucor racemosus and Geotrichum candidum; and a combination thereof.
The method according to claim 2, wherein the chemical asymmetric reduction is achieved with a chiral borane reductant or by asymmetric catalytic hydrogenation or asymmetric catalytic transfer hydrogenation.
The method according to claim 5, wherein the chiral borane reductant is (-)-B-chlorodiisopinocampheylborane or (R)-2-methyl-CBS-oxazaborolidine/borane.
The method according to claim 5, wherein the asymmetric catalytic hydrogenation is carried out by reacting the arylketone of Chemistry Figure 2 with hydrogen gas in the presence of (R)-bisphosphono-ruthenium(II)-(R,R)-chiral diamine complex catalyst.
The method according to claim 5, wherein the asymmetric catalytic transfer hydrogenation is carried out by reacting the arylketone of Chemistry Figure 2 with formic acid triethylamine or isopropanol-inorganic base in the presence of a [S,S]-monosulfonatediamine-M(II)-arene complex catalyst system, wherein M represents ruthenium or rhodium.
The method according to claim 1, wherein the carbamating step is carried out by reacting the alcohol compound of (R)-configuration of Chemistry Figure 5 with inorganic cyanate and an organic acid.
The method according to claim 1, wherein the carbamating step is carried out by hydrolyzing a product resulting from reaction between the alcohol compound of (R)-configuration of Chemistry Figure 5 and an isocyanate compound selected from the group consisting of chlorosulfonic isocyanate, trichloroacetyl isocyanate and trimethylsilyl isocyanate.
The method according to claim 1, wherein the carbamating step is carried out by introducing ammonia into a product resulting from reaction between the alcohol compound of (R)-configuration of Chemistry Figure 5 and a carbonyl compound comprising 1,1'-carbodiimidazole, carbamoylhalide, disuccinyl carbonate, phosgene, triphosgene or chloroformate.
The method according to claim 1, further comprising a crystallizing step after at least one of the (R)-selective asymmetric reduction step and the carbamating step.
The method according to claim 12, wherein the crystallizing step comprises:

adding to a reaction product a solubilizing agent selected from among acetone, acetonitrile, tetrahydrofuran, ethylacetate, dichloromethane, chloroform, 1,4-dioxane, a lower alcohol of 1 to 4 carbon atoms and a mixture thereof; and

adding a precipitating agent thereto selected from the group consisting of water, a lower alcohol of 1 to 4 carbon atoms, diethylether, pentane, hexane, cyclohexane, heptane and a mixture thereof.
The method according to claim 1, additionally including the step of preparing the arylketone of Chemistry Figure 2 is prepared by substitution reaction between an arylketone of the following Chemistry Figure 8 with a tetrazole of the following Chemistry Figure 9:

[Chemistry Figure 8]

[Chemistry Figure 9]

wherein,

R₁ and R₂ are as defined in claim 1; and

X is a leaving group selected from among a halide and a sulfonate;
A method according to claim 14, further comprising a crystallizing step comprising:

adding a solubilizing agent selected from among acetone, acetonitrile, tetrahydrofuran, ethylacetate, dichloromethane, chloroform, 1,4-dioxane, a lower alcohol of 1 to 4 carbon atoms and a mixture thereof to a product obtained by the substitution reaction; and

adding a precipitating agent selected from water, a lower alcohol of 1 to 4 carbon atoms, diethylether, pentane, hexane, cyclohexane, heptanes and a mixture thereof.
A method for preparing an alcohol compound, represented by the following Chemistry Figure 5, through (R)-selective asymmetric reduction of an arylketone, represented by the following Chemistry Figure 2, wherein the (R)-selective asymmetric reduction is achieved by biological asymmetric reduction or chemical asymmetric reduction:

[Chemistry Figure 2]

[Chemistry Figure 5]

wherein,

R₁ and R₂ are independently selected from a group consisting of hydrogen, halogen, perfluoroalkyl, an alkyl of 1 to 8 carbon atoms, a thioalkoxy of 1 to 8 carbon atoms, and an alkoxy of 1 to 8 carbon atoms; and

one of A₁ and A₂ is CH with the other being N.
The method according to claim 16, wherein the biological asymmetric reduction is carried out in a buffer containing the arylketone of Chemistry Figure 2, a microbial strain capable of producing oxidoreductase, and a cosubstrate.
The method according to claim 16, wherein the chemical asymmetric reduction is achieved with a chiral borane reductant or by asymmetric catalytic hydrogenation or asymmetric catalytic transfer hydrogenation.