Synthesis and preparation process of lamivudine intermediate HDMS

A preparation process, lamivudine technology, is applied in the field of synthesis and preparation process of lamivudine intermediate HDMS, which can solve the problems of cost reduction, inconvenient operation, low yield, etc., and achieve cost reduction, stable product quality, Effect of Yield Improvement

Inactive Publication Date: 2010-09-15
ANHUI PROVINCE YIFAN SPICE
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  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0013] The present invention discloses a production process in order to overcome various technical problems such as insufficient mild process conditions, insufficient operation and low yield in the existing HDMS synthesis process in the production process of menthyl glyoxylate CME-I Simple, easy to operate, mild reaction conditions, and a synthetic preparation process with increased yield and greatly reduced cost

Method used

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  • Synthesis and preparation process of lamivudine intermediate HDMS
  • Synthesis and preparation process of lamivudine intermediate HDMS
  • Synthesis and preparation process of lamivudine intermediate HDMS

Examples

Experimental program
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Embodiment

[0040] 1. Preparation of menthyl glyoxylate CME-I:

[0041] Add 250ml of cyclohexane, 260g (1.6667mol) of L-menthol, 42g (0.5676mol) of glyoxylic acid, and 1.5g of concentrated sulfuric acid into a 500ml four-necked bottle, heat up to reflux, and react under reflux for 6 hours. Analyzing the end point of the reaction, CME-I: menthol is about 50: 50, and the water in the reaction is taken out during reflux. After the reaction, the temperature was lowered to 35° C., and the organic layer was washed twice with 2×100 ml of purified water. The organic layer is set aside.

[0042] Add 1000ml of purified water and 50g (0.4807mol) of sodium bisulfite to another 2000ml four-necked bottle, and stir until clarified. Add the above organic layer into the sodium bisulfite solution, and stir at 20-30° C. for 12 hours. The reaction liquid is analyzed by gas chromatography at the end of the reaction, and the CMI-I content is ≤10%. After the reaction was completed, the layers were separated,...

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Abstract

The invention discloses a synthesis and preparation process of a lamivudine intermediate HDMS, which belongs to the field of organic synthetic medicaments. The synthesis and preparation process is characterized in that a preparation method of glyoxylic acid menthol ester comprises the following steps of: under the catalysis of concentrated sulfuric acid, performing a reflux reaction on L-menthol and glyoxylic acid, wherein a reactive solvent is cyclohexane; judging the reaction end point through a gas phase chromatography, and then cooling and washing the mixture; reacting an organic layer with solution of sodium bisulfite at the temperature of between 20 and 30 DEG C; judging the reaction end point through the gas phase chromatography, and then washing the mixture by using the cyclohexane; reacting an aqueous layer with methanol at the temperature of between 20 and 30 DEG C; and washing the mixture after filtering and drying the mixture to obtain the glyoxylic acid menthol ester. By using the synthesis and preparation process, the condition is milder, the operation is simpler and more convenient and the reaction processes are easier to control, so the product production yield and the quality stability are improved, and the cost of the lamivudine intermediate HDMS is greatly reduced.

Description

Technical field: [0001] The invention belongs to the field of organic synthetic medicines, in particular to a synthesis and preparation process of a lamivudine intermediate HDMS. Background technique: [0002] Lamivudine is a drug raw material with good antiviral activity. It is mainly used for anti-hepatitis B and anti-AIDS virus. It is the main active ingredient in the current treatment of hepatitis B and AIDS cocktail therapy. Its synthesis requires the excessive synthesis of intermediates. . [0003] Molecular formula of lamivudine intermediate HDMS: C 15 h 17 o 6 N 3 S.H 2 O, its chemical name: (2R-cis)-4-amino-1-(2-hydroxymethyl-1,3-oxathiolan-5-yl)-1H-pyrimidin-2-one salicyl salt. [0004] English name: 2(R)-(HYDROXY METHYL)-5(S)CYTOSIN-1’-YL-1, 3-OXATHIOLANE SALICYLICACIDSALT. [0005] The structural formula is: [0006] [0007] In the synthesis process of lamivudine intermediate, domestic and foreign public reports, such as US5047407, Xu Fengjie, Yang Y...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): C07D411/04C07C65/10
Inventor 郑家根马守英
Owner ANHUI PROVINCE YIFAN SPICE
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