反应 #1925205

ord-c644e0e02d40468db940c83c0b4cd345

反应条件

详细条件
See reaction.notes.procedure_details.

实验过程

Synthesis of (S)-6-chloro-4-cyclopropylethynyl-4-trifluoromethyl-1,4-dihydro-2H-3,1-benzoxazin-2-one can be accomplished through the use of commercially available 4-chloroaniline. After reaction with pivaloyl chloride in the presence of hydroxide to afford the corresponding amide, treatment with an alkyl lithium and ethyl triflouroacetate is followed by acidification with a mineral acid to provide the salt of the triflouroketone (Scheme 1).

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US06673372B1uspto-grants-2004_01