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ChemicalBook CAS DataBase List Dienogestrel
65928-58-7

Dienogestrel synthesis

9synthesis methods
Dienogest is an orally active synthetic progesterone (or progestin). It is available for use as an oral contraceptive in combination with ethinylestradiol. It has antiandrogenic activity and as a result can improve androgenic symptoms. It is a non-ethinylated progestin which is structurally related to testosterone. Dienogest given in isolation is available for the treatment of endometriosis under the trade name Visanne.
Synthetic Routes
  • ROUTE 1
  • 202112077360530380.jpg

    Liang, Yong; Chen, Bo; Wang, Shaojie. Synthesis of dienogest. Shenyang Yaoke Daxue Xuebao. Volume 28. Issue 10. Pages 788-790. Journal. (2011).

  • ROUTE 2
  • 202112077824472107.jpg

    Chen, Liangkang; Zhang, Peiyi; Chen, Hailin; Chen, Jianxing. Synthesis of dienogest analogues and their biological activity on inhibition of luteal cells. Shengzhi Yu Biyun. Volume 32. Issue 1. Pages 5-9. Journal. (2012).

  • ROUTE 3
  • 202112076663358327.jpg

    Doehler, Thomas; Walther, Dirk; Werner, Michael. Method for synthesis of dienogest from estrone-3-methylether. Assignee Heyl Chemisch-Pharmazeutische Fabrik Gmbh & Co. KG, Germany. US 20100298585. (2010).

  • ROUTE 4
  • 202112076112239534.jpg

    Ding, Li; Li, Jinlu; Chen, Liying. Method for preparation of progestogens-Dienogestril. Assignee Tianjin Pharmaceuticals Research Institute Co., Ltd., Peop. Rep. China. CN 101353365. (2009).

202112077360530380.jpg

Liang, Yong; Chen, Bo; Wang, Shaojie. Synthesis of dienogest. Shenyang Yaoke Daxue Xuebao. Volume 28. Issue 10. Pages 788-790. Journal. (2011).

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Yield:65928-58-7 99.9 %Chromat.

Reaction Conditions:

with perchloric acid in water;acetonitrile at 20 - 30; for 1 h;Reagent/catalyst;Solvent;

Steps:

3 Preparation of Crude Dienogest
The compound (100 g) of example-1 in acetonitrile (600 mL) was cooled to 0-5° C. and 70% perchloric acid (150 mL) was added and stirred for one hour at 20-30° C.
After completion of reaction, water (1500 mL) was added and solid was filtered to obtain crude product. (HPLC data: Dienogest-99.55%, diene impurity-0.125%). Purification of Crude Dienogest a) Wet solid from example-2 was charcoalised in dimethylformamide (400 mL) at 45-50° C. for one hour, filtered, washed with dimethylformamide (100 ml) and to the combined filtrate water (200 ml) was added. Reaction mass stirred for 2 hours at 0-5° C. Solid was filtered and dried under reduced pressure at 40-45° C. to give 66 g crude dienogest. (HPLC data: Dienogest - 99.79%, Diene impurity-0.02%).b) Dienogest (25 g) from example 3(a) was taken in dimethylformamide (125 mL) and heated to 40-50° C., filtered, washed with dimethylformamide (25 ml) and to the combined filtrate water (37.5 ml) was added to precipitate the product, cooled to 0 to 5° C. and stirred for 2 hours. Solid obtained was filtered, washed with water and dried under vacuum at 40-45° C. to give 23 g of Dienogest.(HPLC data: Dienogest - 99.9%, Diene impurity - 0.02%).

References:

LUPIN LIMITED;Tambe, Suhas Ganpat;Kirange, Bhushan Bhanudas;Singh, Gurvinder Pal;Ray, Purna Chandra US2013/41166, 2013, A1 Location in patent:Paragraph 0040

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