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Method for preparing epiandrosterone

An epiandrosterone and ketal technology, applied in the directions of steroids, organic chemistry, etc., can solve the problems of high cost of epiandrosterone raw materials, great potential safety hazard, great environmental damage, etc., and achieves low price, few by-products, and high cost. low cost effect

Active Publication Date: 2016-04-20
仙琚(嘉兴)医药科技有限公司 +1
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0013] The purpose of the present invention is to solve the technical problems of high cost of raw materials currently used to prepare epiandrosterone, high toxicity of some raw materials, great safety hazards and great damage to the environment, and high requirements for equipment due to the need for high pressure

Method used

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Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0051] In the first step, add 4-androstenedione (I) (10g, 0.035mol) and catalyst p-toluenesulfonic acid (2g, 0.01mol) into a 100ml three-necked flask, then add 50ml of acetic anhydride, 2 Under protection, stir the reaction at 25°C for 1h, stop the reaction when there is no raw material detected by thin layer chromatography (TLC), pour into 300ml of ice water to precipitate, stir for 1h, filter with suction, dry at 40°C to obtain the crude esterified product (II) (11.40 g, 0.035 mol). The weight yield is 114%, and the HPLC (High Performance Liquid Chromatography, high performance liquid chromatography) content is 98%;

[0052] In the second step, dissolve the esterified crude product (II) (11.40g, 0.035mol) in a 250ml three-necked flask with 35ml of dichloromethane, then add 23ml of ethylene glycol and 23ml of triethyl orthoformate, and 2 Under protection, 0.3 ml of boron trifluoride diethyl ether was added, and the reaction was carried out at 25° C. for 4 h. Stop the reacti...

Embodiment 2

[0058] In the first step, add 4-androstenedione (I) (10g, 0.035mol) and catalyst pyridine hydrochloride (2g, 0.02mol) into a 100ml three-necked flask, then add 50ml of acetic anhydride, 2 Under protection, stir the reaction at 25°C for 1h, stop the reaction when there is no raw material detected by TLC, pour into 300ml of ice water to precipitate, stir for 1h, filter with suction, and dry at 40°C to obtain the crude esterified product (II) (11.0g, 0.034mol), weight yield 110%, HPLC content 96%;

[0059] Subsequent steps are the same as in Example 1.

Embodiment 3

[0061] In the first step, add 4-androstenedione (I) (10g, 0.035mol), catalyst boron trifluoride ethyl ether (1ml) into a 100ml three-necked flask, and then add 50ml of acetic anhydride. 2 Under protection, stirred and reacted at 25°C for 1h, stopped the reaction when no raw materials were detected by TLC, poured into 300ml of ice water to precipitate, stirred for 1h, filtered with suction, and dried at 40°C to obtain the crude esterified product (II) (11.2g, 0.034mol), weight yield 112%, HPLC content 97%;

[0062] Subsequent steps are the same as in Example 1.

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Abstract

The invention discloses a method for preparing epiandrosterone. 4-androstenedione (I) is used as a raw material to prepare the epiandrosterone. The reaction formula is shown in the description. The low-cost 4-androstenedione is used as the raw material for the first time, and the epiandrosterone is obtained through synthesis on the mild reaction conditions, so that the production cost is greatly lowered, and the method is suitable for large-scale industrial production.

Description

technical field [0001] The invention relates to a method for preparing chemicals, in particular to a method for preparing epiandrosterone. Background technique [0002] Epiandrosterone is a very important pharmaceutical intermediate with a great market prospect. It can be used as a starting material for the synthesis of various drugs such as rocuronium bromide and vecuronium bromide. Rocuronium bromide and vecuronium bromide are currently several non-depolarizing muscle relaxants commonly used clinically. They are clinically used as auxiliary drugs for general anesthesia and are used for tracheal intubation during routine induction of anesthesia to maintain muscle relaxation during surgery. . [0003] The CAS (Chemical Abstracts Service, Chemical Abstracts Service) number of epiandrosterone is 481-29-8, and its structural formula is: [0004] . [0005] Preparation of epiandrosterone in the prior art mainly contains following two kinds of processing routes: [0006] 1....

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): C07J1/00
CPCC07J1/0011
Inventor 戴静刘东华许宏方伟明
Owner 仙琚(嘉兴)医药科技有限公司
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