Literature DB >> 27477654

Convergent Synthesis of Dronedarone, an Antiarrhythmic Agent.

Takashi Okitsu1, Mizuki Ogasahara, Akimori Wada.   

Abstract

We have developed a convergent synthesis of dronedarone, an antiarrhythmic agent. The key steps of the process are the construction of a benzofuran skeleton by iodocyclization and the carbonylative Suzuki-Miyaura cross-coupling for biaryl ketone formation. This synthetic route required only eight steps from 2-amino-4-nitrophenol in 23% overall yield.

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Year:  2016        PMID: 27477654     DOI: 10.1248/cpb.c16-00237

Source DB:  PubMed          Journal:  Chem Pharm Bull (Tokyo)        ISSN: 0009-2363            Impact factor:   1.645


  1 in total

1.  11C-Labeling of Aryl Ketones as Candidate Histamine Subtype-3 Receptor PET Radioligands through Pd(0)-Mediated 11C-Carbonylative Coupling.

Authors:  Fabrice G Siméon; William J Culligan; Shuiyu Lu; Victor W Pike
Journal:  Molecules       Date:  2017-05-12       Impact factor: 4.411

  1 in total

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