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Merck

Facile one-pot synthesis of N-difluoromethyl-2-pyridone derivatives.

Organic letters (2006-08-11)
Makoto Ando, Toshihiro Wada, Nagaaki Sato
摘要

[reaction: see text] A novel one-pot synthesis of N-difluoromethyl-2-pyridones is described. N-(Pyridin-2-yl)acetamide derivatives were excellent precursors for the preparation of N-difluoromethyl-2-pyridone derivatives. Difluoromethylation of 2-acetaminopyridine derivatives was achieved with sodium chlorodifluoroacetate as a difluorocarbene source in the presence of a catalytic amount of 18-crown-6. Subsequent in situ hydrolysis of resultant 1,2-dihydro-2-acetimino-1-difluoromethylpyridines proceeded under mild acidic conditions to afford the corresponding N-difluoromethyl-2-pyridones in moderate to good yields.

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Sigma-Aldrich
2,2-二氟-2-(氟磺酰基)乙酸, 97%
Sigma-Aldrich
5-溴-2(1H)-吡啶酮, 97%