KR20010054545A - Method of synthesizing D(+), L(-)and their ester derivatives - Google Patents

Abstract

PURPOSE: Provided is a process for producing D(+)-, L(-)-malic acid and ester derivatives thereof which are used as components of foods and starting materials of medical supplies and chemicals. CONSTITUTION: The process for producing the D(+)-, L(-)-malic acid (formula III-a, III-b) and the ester derivatives thereof comprises the steps of: reacting cyclic thionocarbonate derivatives of chiral tartaric acid diester with hypophosphorous acid(HPA) at a temperature of 30-100deg.C in the presence of an azobisisobutyronitrile(AIBN) initiator to produce R(+)- and S(-)-chiral malic acid diester derivatives; hydrolyzing the R(+)- and S(-)-chiral malic acid diester derivatives.

Description

Method for preparing D (+), L (-) malic acid and ester derivatives thereof {Method of synthesizing D (+), L (-) and their ester derivatives}

The present invention relates to a novel process for making D (+), L (-) malic acid and ester derivatives thereof, which are usefully used as ingredients of foods or as starting materials for many pharmaceuticals and chemicals.

Conventional methods for preparing the D (+), L (-) malic acid and ester derivatives thereof are described in European Patent 0 802 260 A2 (1997), Japanese Patent 56439 (1982), 204741 (1985), 316491 (1992). , 103680 (1993), 188 (1995), 143891 (1995) US Patent 4,912,042 International Patent 98/10061 (1998), and several known publications (Wynberg, H. et al., Journal of American Chemical Society, Vol. 104). p 166, 1982; Gao, Y. et al., Tetrahedron Letters, Vol. 32. No 27, pp 3155-3158, 1991; Rho, H. Synthetic Communications, Vol. 28. No 5, pp 843-847, Introduced in 1998.

The methods described in these known patents and literature are roughly divided into methods using microorganisms and chemical methods. There are several types and methods of using microorganisms, which have low yields or low optical purity, respectively, and put high-quality inducers into the culture medium or have high activity. There was a restriction to use only species of microorganisms. Chemical methods also have the disadvantages of not being economical by using expensive resolution agents such as quinine, which require several reaction steps, low optical purity, or expensive or toxic agents. There was a problem such as.

SUMMARY OF THE INVENTION An object of the present invention is to provide a method for synthesizing optically active malic acid and its ester derivatives in a manner that is economical, less toxic and easier to handle by solving the disadvantages of the known techniques described above. Synthesis method of the optically active maleic acid and ester derivatives thereof used in the present invention is a relatively easy-to-use and environmentally friendly substance, hypophosphorous acid (HPA) azobisisobutyronitrile (azobisisobutyronitrile; hereinafter AIBN ) To react with cyclic thionocarbonates of (R, R)-and (S, S)-tartaric acid diesters as optically active maleic acid diesters. And hydrolyzing the diester intermediate to produce D (+)-(or R (+)-) and L (-)-(or S (-)-) malic acid.

Synthesis method of the optically active maleic acid and ester derivatives thereof of the present invention is easy to obtain and environmentally friendly materials HPA and AIBN (R, R)-and (S, S)-tartaric acid diesters (tartaric) reacting with cyclic thionocarbonate to produce high yield and optically high purity R (+)-and S (-)-malic acid diesters in near quantitative short time. The ester intermediate is hydrolyzed to produce D (+)-(or R (+)-) and L (-)-(or S (-)-) malic acid of high yield and optical purity.

The process of synthesizing the optically active maleic acid and ester derivatives thereof of the present invention can be represented by the following chemical reaction schemes.

Hereinafter, the method for synthesizing the optically active maleic acid and its ester derivative thereof according to the present invention will be described in more detail.

In the first step, the molar ratio of 1.5 or more (preferably 1.5 to 5.0) for the cyclic thiocarbonates (Ia, b) of the starting materials (R, R)-, and (S, S) -tartaric acid diesters Molar ratio of HPA (50% aqueous solution) and AIBN, a reaction initiator having a molar ratio of 0.05 or more (preferably 0.05 to 1.0 mole), for 30 minutes in a reaction temperature range of 30 to 100 ° C. +)-And S (-)-malic acid diester derivatives (II-a, b) can be obtained in high yield. At this stage, the molar ratio of HPA and AIBN is 3.5 and 0.2, respectively, and the reaction temperature is 80 ° C. with the highest optical purity and yield of R (+)-and S (-)-malic acid diester derivatives (II-a, b) could be obtained. Tetrahydrofuran, acetonitrile, dioxane, N, N-dimethylformamide, and the like can be used as the reaction solvent used for the reaction of this step, but the best results were obtained when using dioxane.

In the second step, a conventional method such as hydrolyzing the R (+)-and S (-)-malic acid diester derivatives (II-a, b) synthesized in the first step, respectively, in the presence of an inorganic base such as caustic soda By hydrolysis by the method, the final products D (+)-and L (-) malic acid (III-a, b) are obtained.

The cyclic thiocarbonates (Ia, Ib) of the starting materials (R, R)-and (S, S)-tartaric acid diesters were (R, R)-and (S, S)-tartaric acid, respectively. Or known methods from (R, R)-and (S, S)-tartaric acid diesters (Corey, EJ et al., Tetrahedron Letters, Vol. 23, pp 1979-1982, 1982; Alpegiani, M. et. al., Journal of Organic Chemistry.Vol. 52, p 278, 1987).

Hereinafter, the preparation method of D (+), L (-) malic acid and ester derivatives thereof of the present invention will be described through several examples. However, each embodiment is for explaining the manufacturing method of the present invention and the present invention is not limited by the following examples.

Example 1 Synthesis of R (+)-Malic Acid Din-Butyl Ester

1.1 Synthesis of Cycric Thiocarbonate of (R, R) -tartaric Acid Din-Butyl Ester

1.58 g (6.02 mmol) of (R, R) -tartaric acid din-butyl ester was added to 50 mL of dichloromethane (CH ₂ Cl ₂ ), followed by dissolving 1.77 g (14.5 mmol) of 4-dimethylaminopyridine. The reaction temperature was then lowered to 0 ° C. and 0.32 mL (4.25 mmol) of thiophosgen was slowly added dropwise over 10 minutes. After stirring for about 1 hour to complete the reaction, it was diluted with dichloromethane (CH ₂ Cl ₂ ) and washed three times with water. After drying using anhydrous magnesium sulfate, the solvent was removed by distillation under reduced pressure, separated by a silica gel column (hexane: methylene chloride = 4: 6) to give a yellow oily product (R, R)-tartaric acid din- 1.5 g (82%) of cyclothiothiocarbonates of butyl ester were obtained. ¹ H NMR (CDCl ₃ ) δ0.87 (t, J = 7 ′, 6H), 1.20-1.73 (s, 8H), 4.29 (t, J = 6.3 Hz, 4H), 5.34 (s, 2H)

1.2 Synthesis of R (+)-maleic acid din-butylester

To 110 mg (0.36 mmol) of cyclic thiocarbonate of (R, R) -tartaric acid din-butyl ester obtained in 1.1, 2 ml of 1,4-dioxane, 0.13 ml (1.26 mmol) of a 50% aqueous solution of HPA, 12 mg (0.072 mmol) of AIBN was added thereto, followed by stirring at 80 ° C. for about 30 minutes. After the reaction was completed, the mixture was diluted with dichloromethane (CH ₂ Cl ₂ ) and washed with saturated aqueous sodium hydrogen carbonate (NaHCO ₃ ). After drying over anhydrous magnesium sulfate, the solvent was removed by distillation under reduced pressure to obtain 82 mg (92%) of the product R (+)-maleic acid din-butyl ester as a colorless oil. ¹ H NMR (CDCl ₃ ) δ 0.93 (t, J = 7 μs, 6H), 1.20-1.73 (m, 8H), 2.78-2.84 (m, 2H), 3.24 (d, J = 5.4 μs, 1H) , 4.05-4.28 (m, 4H), 4.41-4.56 (m, 1H); [a] _D ²⁵ = +10.5 (c 1.1, EtOH)

Example 2 Synthesis of R (+)-Malic Acid Diethyl Ester

2.1 (R, R)-Synthesis of Cycric Thiocarbonate of Tartaric Acid Diethyl Ester

1 g (4.85 mmol) of (R, R) -tartaric acid diethyl ester was added to 40 mL of dichloromethane (CH ₂ Cl ₂ ), followed by dissolving 1.42 g (11.6 mmol) of 4-dimethylaminopyridine. The reaction temperature was lowered to 0 ° C. and 0.44 mL (5.82 mmol) of thiophosgen was slowly added dropwise over 10 minutes. After stirring for 1 hour to complete the reaction, the mixture was diluted with dichloromethane (CH ₂ Cl ₂ ) and washed three times with water. After drying over anhydrous magnesium sulfate, distillation under reduced pressure to remove the solvent, the mixture was separated by a silica gel column (hexane: ethyl acetate = 7: 3) to give a light brown oily product (R, R) -tartaric acid diethyl ester. 1.01 g (84%) of cyclothiothiocarbonate was obtained. ¹ H NMR (CDCl ₃ ) δ 1.36 (t, J = 7 μs, 6H), 4.36 (q, J = 7.2 μs, 4H), 5.36 (s, 2H)

2.2 Synthesis of R (+)-maleic acid diethyl ester

120 mg (0.48 mmol) of cyclic thionocarbonate of (R, R) -tartaric acid diethyl ester, 2 ml of 1,4-dioxane, 0.18 ml (1.69 mmol) of HPA 50% aqueous solution, AIBN 16 Add mg (0.097 mmol) and stir for 3 hours at 80 ℃. After the reaction was completed, the mixture was diluted with dichloromethane (CH ₂ Cl ₂ ) and washed with saturated aqueous sodium hydrogen carbonate (NaHCO ₃ ). After drying over anhydrous magnesium sulfate and distillation under reduced pressure, the solvent was removed to obtain 80 mg (87%) of the product R (+)-malic acid diethyl ester as a colorless oil. ¹ H NMR (CDCl ₃ ) δ 1.20-1.42 (m, 6H), 2.79-2.85 (m, 2H), 3.28 (d, J = 5.3 μs, 1H), 4.07-4.56 (m, 5H); [a] _D ²⁵ = +11.2 (c 0.95, EtOH)

Example 3 Synthesis of R (+)-Malic Acid Dimethyl Ester

3.1 (R, R)-Cyclothiothiocarbonate Synthesis of Tartaric Acid Dimethyl Ester

1 g (5.61 mmol) of (R, R) -tartaric acid dimethyl ester was added to 40 mL of dichloromethane (CH ₂ Cl ₂ ), followed by dissolving 1.65 g (13.5 mmol) of 4-dimethylaminopyridine. The reaction temperature was lowered to 0 ° C., and then 0.51 mL (6.74 mmol) of thiophosgen was slowly added dropwise over 10 minutes. After stirring for about 1 hour to complete the reaction, the mixture was diluted with dichloromethane (CH ₂ Cl ₂ ) and washed three times with water. Dried over anhydrous magnesium sulfate, and then distilled under reduced pressure to remove the solvent, and the resultant was separated by a silica gel column (hexane: methylene chloride = 3: 5: 6: 5) to give a yellow oily product (R, R) -tarta. 1.06 g (85%) of cyclothionocarbonate of lactic acid dimethyl ester was obtained. ¹ H NMR (CDCl ₃ ) δ3.92 (s.6H), 5.40 (s, 2H)

3.2 Synthesis of R (+)-maleic Acid Dimethyl Ester

111 mg (0.50 mmol) of cyclic thionocarbonate of (R, R) -tartaric acid dimethyl ester obtained in 3.1, 2 mL of 1,4-dioxane, 0.18 mL (1.76 mmol) of HPA 50% aqueous solution, 17 mg of AIBN (0.101 mmol) was added and the mixture was stirred at 80 ° C. for about 1 hour. After the reaction was completed, the mixture was diluted with dichloromethane (CH ₂ Cl ₂ ) and washed with saturated aqueous sodium hydrocarbon (NaHCO ₃ ) solution. The remaining NaHCO ₃ layer was washed three more times with dichloromethane (CH ₂ Cl ₂ ). The organic layer was dried over anhydrous magnesium sulfate, and then distilled under reduced pressure to remove the solvent, to obtain 69 mg (85%) of the product R (+)-malic acid dimethyl ester as a colorless oil. ¹ H NMR (CDCl ₃ ) δ2.81-2.87 (m, 2H), 3.40 (d, J = 5.1 ㎐, 1H), 3.72 (s, 3H), 3.82 (s, 3H), 4.45-4.60 (m, 1H); [a] _D ²⁵ = +9.6 (c 2.3, EtOH)

Example 4 Synthesis of D (+)-(or R (+)-) Maleic Acid

246 mg (1.0 mmol) of R (+)-malic acid din-butyl ester synthesized in Example 1 was dissolved in 1.5 ml of water, and 220 mg (5.5 mmol) of caustic soda was dissolved in 2 ml of water at 0 ° C. The mixture was slowly added dropwise over 20 minutes, and the mixture was sufficiently stirred at 20 ° C. for about 2 hours. When the reaction was completed, the resultant was filtered through an ion exchange resin (Dowex 50W), and the filtrate was distilled under reduced pressure to remove water to obtain 123 mg (92%) of white solid crystal D (+)-malic acid. mp = 106-108 ^o C; ¹ H NMR (D ₂ O) δ 3.3 (d, 2H), 4.96 (t, 1H); [a] _D ²⁵ = +28.9 (c 5, pyridine)

Example 5 Synthesis of D (+)-Malic Acid

R (+)-malic acid diethyl ester synthesized in Example 2 was hydrolyzed in the same manner as in Example 4 to obtain D (+)-malic acid in a yield of 92%.

Example 6 Synthesis of D (+)-Malic Acid

R (+)-malic acid dimethyl ester synthesized in Example 3 was hydrolyzed in the same manner as in Example 4 to obtain D (+)-malic acid in a yield of 90%.

Example 7 Synthesis of S (-)-Malic Acid Din-Butyl Ester

7.1 Synthesis of Cycric Thiocarbonates of (S, S) -tartaric Acid Din-Butyl Ester

1.58 g (6.02 mmol) of (S, S) -tartaric acid din-butyl ester was added to 50 mL of dichloromethane (CH ₂ Cl ₂ ), followed by dissolving 1.77 g (14.5 mmol) of 4-dimethylaminopyridine. The reaction temperature was lowered to 0 ° C., and then thiophosgen (0.32 mL, 4.25 mmol) was slowly added dropwise over 10 minutes. After stirring for about 1 hour to complete the reaction, it was diluted with dichloromethane (CH ₂ Cl ₂ ) and washed three times with water. Dried over anhydrous magnesium sulfate, and then distilled under reduced pressure to remove the solvent, and separated by a silica gel column (hexane: methylene chloride = 4: 6) to give a yellow oily product (S, S)-tartaric acid din- 1.47 g (80%) of cyclothiothiocarbonate of butyl ester was obtained. ¹ H NMR (CDCl ₃ ) δ0.87 (t, J = 7 ′, 6H), 1.21-1.72 (s, 8H), 4.28 (t, J = 6.3 Hz, 4H), 5.34 (s, 2H)

7.2 Synthesis of S (-)-maleic acid din-butyl ester

To 110 mg (0.36 mmol) of cyclic thiocarbonate of (S, S) -tartaric acid din-butyl ester obtained in 5.1, 2 ml of 1,4-dioxane, 0.13 ml (1.26 mmol) of a 50% aqueous solution of HPA, 12 mg (0.072 mmol) of AIBN was added thereto, followed by stirring at 80 ° C. for about 30 minutes. After the reaction was completed, the mixture was diluted with dichloromethane (CH ₂ Cl ₂ ) and washed with saturated aqueous sodium hydrogen carbonate (NaHCO ₃ ). After drying using anhydrous magnesium sulfate, the solvent was removed by distillation under reduced pressure to obtain 81.1 mg (91%) of the product S (-)-malic acid din-butyl ester as a colorless oil. ¹ H NMR (CDCl ₃ ) δ 0.93 (t, J = 7 Hz, 6H), 1.21-1.73 (m, 8H), 2.77-2.83 (m, 2H), 3.24 (d, J = 5.4 Hz, 1H) , 4.04-4.28 (m, 4H), 4.41-4.56 (m, 1H)

Example 8 Synthesis of L (-)-(or S (-)-) Maleic Acid

246 mg (1.0 mmol) of S (-)-malic acid di n-butyl ester synthesized in Example 7 was dissolved in 1.5 ml of water, and then 220 mg (5.5 mmol) of caustic soda (NaOH) was dissolved in 2 ml of water. Was slowly added dropwise at 0 ° C. over 20 minutes, and sufficiently stirred at 20 ° C. for about 3 hours. After the reaction was completed, the resultant was filtered through an ion exchange resin (Dowex 50W), and the filtrate was distilled under reduced pressure to remove water, thereby obtaining 122 mg (91%) of white solid crystal L (-)-malic acid. mp = 105-107 ^o C; ¹ H NMR (D ₂ O) δ 3.3 (d, 2H), 4.97 (t, 1H); [a] _D ²⁵ = -29 (c 5.5, pyridine)

The method for preparing D (+), L (-) malic acid and ester derivatives thereof according to the present invention is a relatively inexpensive raw material (R, R)-and (S, S)-tartaric acid or (R, R). -And (S, S)-easily obtainable by using the cyclic thiocarbonates of (R, R)-and (S, S)-tartaric acid diesters which can be easily synthesized from tartaric acid diesters. Hypophosphoric acid and azobisisobutyronitrile, which are environmentally friendly chemicals, can be used as raw materials for pharmaceuticals and chemicals, such as D (+), L (-) malic acid and D (+)-, L (- )-Provides a useful method for synthesizing maleic acid ester derivatives in a short time with high purity and high yield.

Claims (7)

Structural formula (II-a) by reacting cyclic thiocarbonate derivatives of the optically active tartaric acid diesters of formulas (I-a) and (I-b) of Schemes 3 and 4 with hypophosphorous acid (HPA) And (II-b) to prepare R (+) and S (-)-optically active maleic acid diester derivatives. The optically active maleic according to claim 1, wherein the solvent used in the reaction for preparing the optically active maleic acid diester derivative is one of tetrahydrofuran, acetonitrile, dioxane or N, N-dimethylformamide. Method for preparing acid diester derivative. The method for producing an optically active maleic acid diester derivative according to claim 1 or 2, wherein the reaction is performed at a temperature in the range of 30 to 100 ° C. The optically active maleic acid di according to claim 1 or 2, wherein the molar ratio of the cyclic thionocarbonate derivative of the optically active tartaric acid diester and hypophosphorous acid (HPA) in the reaction is 1.5 or more. Method for preparing ester derivatives. The method of claim 1, wherein azobisisobutyronitrile (AIBN) is used as an initiator to increase the reaction efficiency. 6. The optically active maleic acid preparation according to claim 5, wherein the azobisisobutyronitrile (AIBN) is used at a molar ratio of 0.05 or more with respect to the cyclic thiocarbonate derivative of the optically active tartaric acid diester. Way. D (+)-and L (-)-of Scheme 3 or 4 by hydrolyzing the R (+) and S (-)-optically active maleic acid diester derivatives prepared in claim 1 by a conventional hydrolysis method. Process for preparing optically active maleic acid (III-a, III-b).