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Method for purifying ulipristal serving as synthetic progesterone receptor regulator

A purification method, a Uliplast-style technology, applied in the field of progesterone receptor modulator Uliplast acetate, which can solve the problem that the purity of the final product is difficult to control, the intermediates Uliplast and demethylated Ulipast Extraordinary residues and other issues

Active Publication Date: 2011-11-16
杭州容立医药科技有限公司
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

The purity of the final product obtained by this method is not easy to control, and the uncompleted intermediate uliplast and demethylated uliplast have relatively large residues

Method used

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  • Method for purifying ulipristal serving as synthetic progesterone receptor regulator
  • Method for purifying ulipristal serving as synthetic progesterone receptor regulator
  • Method for purifying ulipristal serving as synthetic progesterone receptor regulator

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0015] 1) 40 g of the crude product of uliplast acetate was concentrated and dried with 60 g of silica gel (1.5 times) for sample loading, passed over 800 g of silica gel (200-300 mesh silica gel, 20 times the weight consumption), and dichloromethane: acetone = 20:1 After elution, the product was collected and concentrated to dryness to obtain 35 g of the desired product.

[0016] 2) After concentrating to dryness, 35 g of uliplast acetate was dissolved in 105 ml of ethyl acetate, 315 ml of petroleum ether was added, and stirred for one hour. Then filter. The solid was washed twice with 50 ml of a mixed solution of petroleum ether: ethyl acetate = 5:1. Dry under reduced pressure. 32 g of white solid powder were obtained.

[0017] 3) Dissolve 32 grams of white solid powder in 300ml of absolute ethanol, add 360ml of water under reflux conditions under controlled temperature (70~75°C), and let stand to cool down to room temperature. The crystals were filtered and dried under ...

Embodiment 2

[0019] 1) 80 g of the crude product of uliplast acetate was concentrated and dried with 120 g of silica gel, and then passed through 2400 g of silica gel (200-300 mesh silica gel, 30 times the amount by weight), eluted with dichloromethane: acetone = 10: 1, and collected The product was concentrated to dryness to obtain 70g of the desired product.

[0020] 2) After concentrating to dryness, 70 g of uliplast acetate was dissolved in 210 ml of ethyl acetate, 210 ml of petroleum ether was added, and stirred for one hour. Then filter. The solid was washed twice with 100 ml of petroleum ether:ethyl acetate=1:1 mixed solution. Dry under reduced pressure. 58 g of white solid powder were obtained.

[0021] 3) Dissolve 58 grams of white solid powder in 500ml of absolute ethanol, add 500ml of water under reflux under controlled temperature (70~75°C), and let stand to cool down to room temperature. The crystals were filtered and dried under reduced pressure at 40°C to obtain 52 g of ...

Embodiment 3

[0023] 1) Concentrate 60 g of the crude product of Uliplast Acetate with 100 g of silica gel (1.5 times) to dry and load the sample, pass through 900 g of silica gel (200-300 mesh silica gel), elute with dichloromethane: acetone = 15: 1, and collect the product , and concentrated to dryness to obtain 52g of the desired product.

[0024] 2) After concentrating to dryness, 52 g of uliplast acetate was dissolved in 156 ml of ethyl acetate, 780 ml of petroleum ether was added, and stirred for one and a half hours. Then filter. The solid was washed twice with 60 ml of a mixed solution of petroleum ether:ethyl acetate=5:1. Dry under reduced pressure. 49 g of white solid powder were obtained.

[0025] 3) Dissolve 49 grams of white solid powder in 300ml of absolute ethanol, add 450ml of water under reflux conditions under controlled temperature (70~75°C), and let stand to cool down to room temperature. The crystals were filtered and dried under reduced pressure at 40°C to obtain 4...

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Abstract

The invention provides a method for purifying ulipristal serving as a synthetic progesterone receptor regulator. By adopting the method, high-purity ulipristal acetate can be obtained by quickly removing various impurities. The method is easy and convenient to operate, high in yield and suitable for industrial production.

Description

technical field [0001] The present invention relates to a progesterone receptor modulator ulipristal acetate (ulipristal acetate), that is, 17α-acetoxy-11β-[4-(N,N-dimethylamino)-phenyl]- Novel purification method for 19-norpregna-4,9-diene-3,20-dione. technical background [0002] Ulipristal acetate (formula I) is a progesterone receptor modulator with progesterone receptor antagonistic and partial agonistic activity. The drug has been developed by HRA Pharmaceuticals and was approved by the European Commission in May 2009 as an emergency contraceptive for women to use within 5 days of unprotected intercourse or contraceptive failure. [0003] [0004] One of the typical synthetic methods of uliplast acetate drug has been disclosed in US Pat. No. 5,929,262. The final product obtained by the method described in Example 7 of said US Patent 5,929,262 is described as a product in the form of yellow crystals with a melting point between 183 and 185°C. The presence of said ...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): C07J41/00
Inventor 李航王万青何党军
Owner 杭州容立医药科技有限公司
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