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屈螺酮的合成方法综述

Summary of the Synthetic Methods of Drospirenone
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摘要 屈螺酮是一种高效、低毒、安全性好的新一代孕激素,具有良好的天然孕酮活性。屈螺酮通常与炔雌醇组成复方雌孕激素制剂,临床上被用来作为女性口服避孕药。本文综述了近些年屈螺酮的合成路线并简单展望了其后续的合成工艺改进方向。 Drospirone is a new generation of progesterone with high efficiency,low toxicity and good safety,which owned excellent natural progesterone activity.Drospirone is usually combined with ethinylestradiol to form a compound estrogen and progesterone preparation,which is clinically used as an oral contraceptive for women.This paper reviews the synthetic routes of drospirone in recent years,and briefly looks forward to the improvement direction of its subsequent synthetic process.
作者 叶有志 潘建洪 隋志红 金旦妮 YE You-zhi;PAN Jian-hong;SUI Zhi-hong;JIN Dan-ni(Taizhou Xianju Pharmaceutical Co.,Ltd.,Taizhou,Zhejiang 317016,China)
出处 《浙江化工》 CAS 2021年第12期9-13,18,共6页 Zhejiang Chemical Industry
关键词 避孕药 孕激素 屈螺酮 合成 contraceptive progesterone drospirenone synthesis
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  • 1何明华,廖清江.曲螺酮的合成[J].中国新药杂志,2006,15(20):1756-1759. 被引量:10
  • 2BITTLER D, HOFMEISTER H, LAURENT H, et al.Synthesis of spirorenone-A novel highly active aldosterone antagonist [ J ]. Angew Chem Int Ed Engl, 1982,21 (9) :696 - 697.
  • 3GALIK G, HORVATH J, SOROS B, et al. A process for the preparation of 17-hydroxy-6β,7β; 15β, 16β- bismethylene- 17α-pregn-4-en-3 -one-21 -carboxy acid γ-laetone and key-intermediates for this process: WO,2006/059168A1 [ P]. 2006 - 06 - 08.
  • 4SOROS B,HORVATH J,GALIK G,et al. Industrial process for the preparation of 17-hydroxy-6β, 7β; 15β, 16β-bismethylene-3-oxo-17 α-pregn-4-ene-21- carboxylic acid γ-lactone and key-intermediates for this process: WO,2006/059167 [ P ]. 2006 - 06 - 08.
  • 5PETZOLDT K,LAURENT H,WIECHERT R. A novel synthetic route to the aldosterone-antagonist spirorenone[ J]. Angew Chem Int Ed Engl, 1983,22 (5) :406 -407.
  • 6PETZOLDT K, LAURENT H, WIECHERT R. 3β, 7β, 15α-Trihydroxy-5-androsten-17-one, its 3, 15- dipivalate, and their preparation: US, 4435327 [ P ]. 1984 - 03 - 06.
  • 7KELLY R W, SYKES P L Synthetic steroids. Part Ⅲ. The preparation of 3β, 15α, 17β-trihydroxyandrost-5-ene and the attempted preparation of 3β, 15α, 17β-trihydroxyandrost-5-ene[ J]. J Chem Soc (C), 1968:416 -421.
  • 8KAMERNISKII A V,GALAKHOVA T N,LEVINA I S, et al. The synthesis of 3β-hydroxy-15α, 16α- methyleneandrost-5-ene-17-one [ J ]. Bull Acad Sci USSR Chem Sci, 1985,34:1743.
  • 9李援朝,姜标,邓刚,等.屈螺酮立体选择性化学合成新方法:中国,101177446A[P].2008-05-14.
  • 10GALLIANI G,RADAELLI V, TERRANEO A. Process for the preparation of drospirenone: WO, 2009/059765A2 [ P]. 2009 - 05 - 14.

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