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ChemicalBook CAS DataBase List Dronedarone

Dronedarone synthesis

4synthesis methods
Dronedarone is an antiarrhythmic, acting as a multichannel blocker. Dronedarone inhibits multiple outward potassium currents and reduces inward rapid Na current and L-type Ca channels.
Synthetic Routes
  • ROUTE 1
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    Process for the preparation of dronedarone; Gutman, Arie L.; Nisnevich, Gennady; Yudovitch, Lev; Assignee ISP Investments Inc., USA 2003; Patent Information; May 15, 2003; WO 2003040120 A1

  • ROUTE 2
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    Process for preparation of Dronedarone and synthetic intermediates thereof; Marom, Ehud; Mizhiritskii, Michael; Rubnov, Shai; Assignee Mapi Pharma Holdings (Cyprus) Limited, Cyprus 2011; Patent Information; Aug 18, 2011; WO 2011099010 A1

  • ROUTE 3
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    Process for the preparation of 3-aroyl-5-aminobenzofuran derivatives; Richter, Frank; Schreiner, Erwin; Pirc, Samo; Copar; Anton Assignee Lek Pharmaceuticals d.d., Slovenia 2012; Patent Information; May 18, 2012; WO 2012062918 A1

  • ROUTE 4
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    Rajan, Srinivasan Thirumalai; Eswaraiah, Sajja; Satyanarayana, Komati. Process for the preparation of dronedarone an known antiarrhythmic agent. Assignee MSN Laboratories Limited, India. IN 2012CH03310. (2016).

  • ROUTE 5
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    Bollikonda, Satyanarayana; Mohanarangam, Saravanan; Chaganti, Sridhar; Jinna, Rajender Reddy; Madaraboina, Mahender. Process for the preparation of dronedarone and pharmaceutically acceptable salts thereof. Assignee Dr. Reddy's Laboratories Limited, India; Dr. Reddy's Laboratories Inc. IN 2010CH01080. (2012).

  • ROUTE 6
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    Zhou, Xinji; Mao, Jincheng; Zhu, Jianjun; Li, Xunxun. A process for preparing dronedarone. Assignee Jiangsu Jiujiujiu Technology Co., Ltd., Peop. Rep. China. CN 103450124. (2013).

  • ROUTE 7
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    Li, Feng; Jin, Chunhua; Zou, Jianwei; Wu, Jun. A facile and efficient synthesis of dronedarone hydrochloride. Bulletin of the Korean Chemical Society. Volume 35. Issue 7. Pages 1970-1972. 2014.

  • ROUTE 8
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    Biard, Michel. 2-Butyl-3-(4-[3-(dibutylamino)propoxy]benzoyl)-5-nitro-benzofuran hydrochloride and preparation thereof. Assignee Sanofi-Synthelabo, Fr.. WO 2002048078. (2002).

  • ROUTE 9
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    Mali, Anil C.; Ippar, Sharad S.; Bodke, Mahendra B.; Patil, Nilesh S.; Mathad, Vijayavitthal T. An Improved and Efficient Process for the Production of Dronedarone Hydrochloride, an Antiarrhythmia Drug. Organic Process Research & Development. Volume 17. Issue 5. Pages 863-868. 2013.

  • ROUTE 10
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    Mahender, M.; Saravanan, M.; Sridhar, Ch.; Chandrashekar, E. R. R.; Kumar, L. Jaydeep; Jayashree, A.; Bandichhor, Rakeshwar. Identification and Characterization of Potential Impurities of Dronedarone Hydrochloride. Organic Process Research & Development. Volume 18. Issue 1. Pages 157-162. 2014.

202112075122289661.jpg

Process for the preparation of dronedarone; Gutman, Arie L.; Nisnevich, Gennady; Yudovitch, Lev; Assignee ISP Investments Inc., USA 2003; Patent Information; May 15, 2003; WO 2003040120 A1

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Yield:141626-36-0 79%

Reaction Conditions:

with pyridine in butan-1-ol at 70; for 14 h;

Steps:

2
0.8 g of N- [2-butyl-3 - { 4- [(3 -amino)propoxy] benzoyl } - 1 -benzofuran-5- yl]methanesulfonamide (II) is dissolved in 5 ml of n-butanol. 0.15 g of pyridine is added and the mixture is heated to 70 °C at this temperature 0.68 g of butyl-methanesulfohate (III) dissolved in 1 ml of n-butanol is added during 15 minutes and the mixture is kept at 70 °C for 14 hours. [The methanesulfonate is prepared according to the procedure described in J. of Steroid Biochemistry and Molecular Biology 80 (2002) 429-440.] The reaction mixture is evaporated and 20 ml of dichloromethane and 10 ml of water is added. The phases are separated. The organic phase is washed with 10ml of NaHC03 of 5 %. The organic phase is evaporated. The product is purified by on silica gel (ethyl acetate/hexane; 1 :3 v/v ).Yield: 0.79 g (79 %). Purity: 100 % (HPLC).The product is identical with the compound prepared in example 1.

References:

SANOFI;FRIESZ, Antal;PÁRKÁNYI, Zsolt;DOMBRÁDY, Zsolt WO2012/131409, 2012, A1 Location in patent:Page/Page column 14-15

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