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ChemicalBook CAS DataBase List Alfuzosin hydrochloride
81403-68-1

Alfuzosin hydrochloride synthesis

8synthesis methods
Alfuzosin HCl is a pharmaceutical drug of the alpha-1 blocker class. As an antagonist of the alpha-1 adrenergic receptor, it works by relaxing the muscles in the prostate and bladder neck, making it easier to urinate. It is thus used to treat benign prostatic hyperplasia (BPH). Alfuzosin is marketed in the United States by Sanofi Aventis under the brand name Uroxatral and elsewhere under the tradename Xat or Xatral, and in Egypt under name of Prostetrol. Alfuzosin was approved by the FDA for treatment of BPH in June 2003.
Synthetic Routes
  • ROUTE 1
  • 202112077507380032.jpg

    Manoury, Philippe M.; Binet, Jean L.; Dumas, Andre P.; Lefevre-Borg, Francoise; Cavero, Icilio. Synthesis and antihypertensive activity of a series of 4-amino-6,7-dimethoxyquinazoline derivatives. Journal of Medicinal Chemistry. Volume 29. Issue 1. Pages 19-25. 1986.

  • ROUTE 2
  • 202112070059522123.jpg

    Zhu, Xingyan; Wang, Yanyan; Di, Yan; Jiang, Fang; Xu, Youjun. Improved synthesis of alfuzosin hydrochloride. Zhongguo Yaowu Huaxue Zazhi. Volume 19. Issue 5. Pages 352-355. 2009.

  • ROUTE 3
  • 202112071663182421.jpg

    Zhang, Zhiyong. Synthesis of Alfuzosin hydrochloride. Zhongguo Yiyao Gongye Zazhi. Volume 32. Issue 7. Pages 289-291. 2001

  • ROUTE 4
  • 202112073342795053.jpg

    Xu, Jing; He, Zhan; Song, Hongrui. Improved synthesis of alfuzosin hydrochloride. Jingxi Huagong Zhongjianti. Volume 40. Issue 3. Pages 40-43. 2010.

  • ROUTE 5
  • 202112078697997149.jpg

    Chen, Xian; Zhang, Qi; Li, Ying; Shi, Daxin; Li, Jiarong. An improved synthesis method of alfuzosin hydrochloride. Jingxi Huagong. Volume 28. Issue 7. Pages 710-713. 2011.

  • ROUTE 6
  • 202112071232101065.jpg

    Wang, Haiyan; Luo, Wengong; Zhang, Lulu. Improved process for preparing Alfuzosin hydrochloride. Assignee Liaoning Keji Pharmaceutical Co., Ltd., 2018.

  • ROUTE 7
  • 202112076129244983.jpg

    Keshav, Deo; Sanjay, Desai; Mohansihn, Rathod Dhiraj; Chandrakant, Parikh Chirag; Kantibhai, Patel Ripalkumar; Suresh, Mistry Chirayu. A process for the preparation of alfuzosin hydrochloride. Assignee Alembic Limited, India. 2010.

  • ROUTE 8
  • 202112073080965622.jpg

    Zhang, Peng. Process for preparing Alfuzosin hydrochloride. Assignee Liaoning Keji Pharmaceutical Co., Ltd. 2017.

  • ROUTE 9
  • 202112075987303527.jpg

    Li, Jiarong; Shi, Daxin; Chen, Xian; Zhang, Qi; Li, Ying. Method for preparation of Alfuzosin hydrochloride. Assignee Beijing Institute of Technology. 2010.

  • ROUTE 10
  • 202112073725143865.jpg

    Sadanand, Nadkarni Sunil; Bhivsan, Ahire Prakash; Chandrakantrao, Joshi Uday. Preparation of alfuzosin. Assignee Torrent Pharmaceuticals Limited. 2007.

202112077507380032.jpg

Manoury, Philippe M.; Binet, Jean L.; Dumas, Andre P.; Lefevre-Borg, Francoise; Cavero, Icilio. Synthesis and antihypertensive activity of a series of 4-amino-6,7-dimethoxyquinazoline derivatives. Journal of Medicinal Chemistry. Volume 29. Issue 1. Pages 19-25. 1986.

81403-80-7 Synthesis
Alfuzosin

81403-80-7
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Yield:81403-68-1 88%

Reaction Conditions:

with hydrogenchloride in ethanol at 20 - 25;

Steps:

4
Example 4:Preparation of anhydrous Alfuzosin hydrochloride: Alfuzosin base (5g, 0.013mol) is charged to a flask and ethanol (110ml) added. The mixture is refluxed for 15 min. and the solid dissolved. Activated charcoal is added to this solution and the suspension is stirred for lOmin., filtered and washed with 5ml hot ethanol. The filtrate is cooled down to 20-250C and the ethanol saturated by hydrogen chloride gas (1.5ml) is added. Then diethyl ether (25ml) and water (0.09ml) were slowly added to the mixture. The mixture is then stirred at room temperature for 20 hours. The mixture is then cooled down to 0-50C and after stirring for one hour the product is filtered off and washed with 7.5ml of diethyl ether. The crystalline product is dried in a vacuum drier at 12O0C for minimum 8 hours. The yield of alfuzosin hydrochloride is 4.85g (88%).

References:

UNICHEM LABORATORIES LIMITED WO2008/84493, 2008, A2 Location in patent:Page/Page column 9-10

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