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An Efficient Synthesis of 2-(2,2-difluoroethoxy)-6-trifluoromethyl- n -(5,8-dimethoxy-1,2,4-triazolo[1,5-c]pyrimidine-2-yl) Benzenesulfonamide: Penoxsulam

An efficient nine-step synthesis of 2-(2,2-difluoroethoxy)-6-trifluoromethyl- N-(5,8-dimethoxy-1,2,4-triazolo[1,5-c] -pyrimidine-2-yl) benzenesulfonamide has been developed. The starting material 4-nitro-2-(trifluoromethyl)aniline starting material was converted via 2-bromo-4-amino-6-trifluoromethyl...

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Published in:Journal of chemical research 2013-04, Vol.37 (4), p.197-200
Main Authors: Wu, Feifei, Gao, Shiguang, Chen, Zhiyin, Su, Jinyue, Zhang, Dayong
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Language:English
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cited_by cdi_FETCH-LOGICAL-c370t-de00a404064f6b1cb7f8c84bdc42931f057689aec493538f287ae73e75a417d43
cites cdi_FETCH-LOGICAL-c370t-de00a404064f6b1cb7f8c84bdc42931f057689aec493538f287ae73e75a417d43
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container_title Journal of chemical research
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creator Wu, Feifei
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Chen, Zhiyin
Su, Jinyue
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description An efficient nine-step synthesis of 2-(2,2-difluoroethoxy)-6-trifluoromethyl- N-(5,8-dimethoxy-1,2,4-triazolo[1,5-c] -pyrimidine-2-yl) benzenesulfonamide has been developed. The starting material 4-nitro-2-(trifluoromethyl)aniline starting material was converted via 2-bromo-4-amino-6-trifluoromethylaniline and 2-bromo-4-acetamido-6-trifluoro-methylbenzenesulfonic acid to 2-bromo-6-trilfuoromethylbenzenesulfonic acid. This was then combined with 2-amino-5,8-dimethoxy-1,2,4-triazolo[1.5-c]pyrimidine to give the target molecule. Compared with the reported method, this approach has advantages in its shorter reaction time, milder reaction conditions and easier purifiction. Moreover, the overall yield has been improved to 22.9% which is twice of that of the reported method.
doi_str_mv 10.3184/174751913X13619014318618
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The starting material 4-nitro-2-(trifluoromethyl)aniline starting material was converted via 2-bromo-4-amino-6-trifluoromethylaniline and 2-bromo-4-acetamido-6-trifluoro-methylbenzenesulfonic acid to 2-bromo-6-trilfuoromethylbenzenesulfonic acid. This was then combined with 2-amino-5,8-dimethoxy-1,2,4-triazolo[1.5-c]pyrimidine to give the target molecule. Compared with the reported method, this approach has advantages in its shorter reaction time, milder reaction conditions and easier purifiction. 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title An Efficient Synthesis of 2-(2,2-difluoroethoxy)-6-trifluoromethyl- n -(5,8-dimethoxy-1,2,4-triazolo[1,5-c]pyrimidine-2-yl) Benzenesulfonamide: Penoxsulam
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