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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 558575생성일: 2026년 10월 26일

4,4,4-Trifluoro-1-(4-trifluoromethylphenyl)-1,3-butanedione → 4-Trifluoromethyl-2-(4-trifluoromethyl-phenyl)-imidazo[1,5-a]pyrimidine-8-carboxylic acid ethyl ester

https://huagongshe.com/reaction/558575

반응식

참여 물질

역할이름HCID투입량
반응물4,4,4-Trifluoro-1-(4-trifluoromethylphenyl)-1,3-butanedioneHCID 10859020—
반응물HCID 178470302HCID 178470302—
용매Acetic AcidHCID 176—
생성물4-Trifluoromethyl-2-(4-trifluoromethyl-phenyl)-imidazo[1,5-a]pyrimidine-8-carboxylic acid ethyl esterHCID 8660800343.5%

반응 단계

A mixture of 4,4,4-trifluoro-1-(4-trifluoromethyl-phenyl)-butane-1,3-dione (10.0 g, 35.2 mmol) and 5-amino-1H-imidazole-4-carboxylic acid ethyl ester (5.0 g, 32.2 mmol) in acetic acid (120 mL) was refluxed for 24 h and evaporated. The crude product was further purified by column chromatography on silica gel (ethyl acetate/heptane) and crystallization (diethyl acetate/hexane) to yield 4-trifluoromethyl-2-(4-trifluoromethyl-phenyl)-imidazo[1,5-a]pyrimidine-8-carboxylic acid ethyl ester (5.65 g, 43%) as a yellow solid. MS (EI) 403.1 [(M)+]; mp 243° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08063048B2
출처 데이터셋uspto-grants-2011_11
ORD IDord-d0887e86b248414ab97e080a2bc9ddf2
출처 메모uspto-grants-2011_11