Ethyl 4,4,4-trifluoro-3-oxo-butyrate reacted with 2,6-dimethyl-3,5-diacetyl-pyridine 1 in the presence of NaOC2H5 at 0 ℃ to give 2,6-dimethyl-3,5-bis（4,4,4-trifluoro-1,3-oxo-butyl）-pyridine （2a） in good yield. Cy...Ethyl 4,4,4-trifluoro-3-oxo-butyrate reacted with 2,6-dimethyl-3,5-diacetyl-pyridine 1 in the presence of NaOC2H5 at 0 ℃ to give 2,6-dimethyl-3,5-bis（4,4,4-trifluoro-1,3-oxo-butyl）-pyridine （2a） in good yield. Cyclization reaction of 2a and aryl imidoyl chlorides 5a--5i, obtained from chlorination of aryl oximes with N-chlorosuccimide, afforded 2,6-dimethyl-3,5-bis[（3-aryl-5-trifluoromethyl）-isoxazol-4-carbonyl]-pyridine derivatives 6a=6i.展开更多
基金Acknowledgement The authors thank the National Natural Science Foundation of China （NNSFC） （Nos. 21072128, 21272153）, the Key Laboratory of Organofluorine Chemistry, Shanghai Institute of Organic Chemistry for financial support.
文摘Ethyl 4,4,4-trifluoro-3-oxo-butyrate reacted with 2,6-dimethyl-3,5-diacetyl-pyridine 1 in the presence of NaOC2H5 at 0 ℃ to give 2,6-dimethyl-3,5-bis（4,4,4-trifluoro-1,3-oxo-butyl）-pyridine （2a） in good yield. Cyclization reaction of 2a and aryl imidoyl chlorides 5a--5i, obtained from chlorination of aryl oximes with N-chlorosuccimide, afforded 2,6-dimethyl-3,5-bis[（3-aryl-5-trifluoromethyl）-isoxazol-4-carbonyl]-pyridine derivatives 6a=6i.
