A kind of synthetic method of d-cycloserine intermediate

A technology of serine methyl ester and alanine methyl ester, which is applied in the field of medicine, can solve the problems of high price of thionyl bromide, potential safety hazards, and many by-products, so as to facilitate industrial scale-up, improve operation safety, and improve reaction conditions. mild effect

Active Publication Date: 2019-03-19
ZHEJIANG HISUN PHARMA CO LTD
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

The method takes D-serine methyl ester hydrochloride as raw material, generates D-2-amino-3-chloropropionic acid methyl ester hydrochloride in chloroform with phosphorus pentachloride generation chlorination reaction, and this technique has the following points Insufficient: First, the PCl used 5 It is a solid powder with high risk and is not easy to feed. The second is PCl 5 When used as a chlorination reagent, a large amount of waste acid (4eq of HCl and 1eq of H 3 PO 4 ), the third is to react at low temperature (-20 ~ -15 ℃), the energy consumption is large, and the product is not easy to filter
[0010] This patent document further points out, in order to be able to reach higher yield, this reaction preferably carries out under the existence of HCl gas, and the shortcoming of this method is: (1) raw material HCl is gas, is stored in compressed cylinder, uses (2) HCl gas will have a certain corrosive effect on equipment during the scale-up production process; (3) when the process wants to obtain a higher yield in the reaction process, the usage of HCl gas needs to be within the substrate More than 3 molar equivalents, a large amount of waste acid will eventually be formed
[0011] Hee-Kwon Kim etc. reported a kind of synthetic method for preparing 3-bromoalanine methyl ester hydrobromide in document Simple and efficient synthetic routes to D-cycloserine (Tetrahedron Letters 53 (2012) 1668-1670), the The process uses D-serine methyl ester hydrochloride as the starting material, cyclohexane as the reaction solvent, and thionyl bromide as the halogenation reagent to generate 3-bromoalanine methyl ester hydrobromic acid under the catalysis of DMF. Salt, the defect of this technique is: (1) the price of the halogenated reagent dibromoxide thionyl used in this technique is on the high side, and atom economy is lower compared with thionyl chloride; (2) the total yield of this technique is low ( 85%), many by-products
[0013] The above disclosed 3-halo-D-alanine methyl ester acid salts or their analogues have defects in the synthesis and cannot meet the needs of industrial production. Therefore, there is an urgent need for a method that is easy to operate, safe, mild in conditions, and low in cost. and environmentally friendly production process

Method used

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  • A kind of synthetic method of d-cycloserine intermediate
  • A kind of synthetic method of d-cycloserine intermediate
  • A kind of synthetic method of d-cycloserine intermediate

Examples

Experimental program
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Effect test

Embodiment 1

[0025] In a 1L four-necked flask, add 150ml of acetonitrile and 450ml of dichloromethane, weigh 60g of D-serine methyl ester hydrochloride (0.386mol) into the mixed solvent, stir evenly, cool down to 0°C, and then slowly add SOCl 2 34.4ml (0.463mol), keep the temperature at 0°C, add SOCl 2 Afterwards, the temperature was raised to 30°C. After reacting for 12 hours, 61.4 g of white solid (purity 96.8%) was obtained by filtration, and the product yield was 88.5%.

Embodiment 2

[0027] In a 1L four-necked flask, add 200ml of acetonitrile and 400ml of dichloromethane, weigh 60g of D-serine methyl ester hydrochloride (0.386mol) into the mixed solvent, stir evenly, cool down to 0°C, and then slowly add SOCl 2 34.4ml (0.463mol), keep the temperature at 0°C, add SOCl 2 Afterwards, the temperature was raised to 30°C. After reacting for 12 hours, 63.4 g (purity: 97%) of white solid was obtained by filtration, and the yield was 91.6%.

Embodiment 3

[0029] In a 1L four-neck flask, add 300ml of acetonitrile and 300ml of dichloromethane, weigh 60g of D-serine methyl ester hydrochloride (0.386mol) into the mixed solvent, stir evenly, cool down to 0°C, and then slowly add SOCl 2 34.4ml (0.463mol), keep the temperature at 0°C, add SOCl 2 Afterwards, the temperature was raised to 20°C. After reacting for 12 hours, 64.92 g (purity: 97%) of a white solid was obtained by filtration, and the yield was 93.8%.

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Abstract

Disclosed is a method of synthesizing a 3-halo-D-alanine methyl ester or an acid salt thereof. By reacting a D-serine methyl ester or an acid salt thereof and a halogenation reagent in an organic solvent, the method prepares a 3-halo-D-alanine methyl ester or an acid salt thereof. The compound is an important intermediate for preparing a D-cycloserine. The method and process employed in the present invention are easy to operate and highly safe, require a moderate reaction condition, have a high yield, and are low in cost, and reduce waste acid generation considerably and are suitable for industrial production.

Description

technical field [0001] The invention belongs to the technical field of medicine, and in particular relates to a synthesis method of a D-cycloserine intermediate. Background technique [0002] As a second-line anti-tuberculosis drug, D-cycloserine has a relatively broad market prospect because its drug resistance occurs more slowly than other anti-tuberculosis drugs and there is no cross-resistance with other anti-tuberculosis drugs. Chemical name: D-4-amino-3-tetrahydroisoxazolone; its structural formula is as follows: [0003] [0004] The synthesis methods of D-cycloserine reported in the literature generally use D-serine or D-serine methyl ester acid salt as the starting material, and all of them must go through two steps of halogenation and cyclization to obtain D-cycloserine. 3-Halo-D-alanine methyl ester or its acid salt is an important intermediate for the preparation of D-cycloserine, wherein the halogenation step is a difficult point in the entire process of pre...

Claims

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Application Information

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Patent Type & Authority Patents(China)
IPC IPC(8): C07C227/16C07C229/20
CPCC07C227/16C07C229/20
Inventor 傅德进吴植献杨勇温伟江
Owner ZHEJIANG HISUN PHARMA CO LTD
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