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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 655792생성일: 2026년 10월 25일

Tri-o-tolylphosphine → N-[3-[2-[6-(Methylamino)-9H-purine-9-yl]ethenyl]-4-methylphenyl]-3-(trifluoromethyl)benzamide

https://huagongshe.com/reaction/655792

반응식

참여 물질

역할이름HCID투입량
반응물Tri-o-tolylphosphineHCID 80271—
반응물DiisopropylethylamineHCID 81531—
반응물N-(3-iodo-4-methylphenyl)-3-(trifluoromethyl)benzamideHCID 7925506—
반응물N-Methyl-9-vinyl-9H-purin-6-amineHCID 23649897—
촉매palladium(II) acetateHCID 167845—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
생성물N-[3-[2-[6-(Methylamino)-9H-purine-9-yl]ethenyl]-4-methylphenyl]-3-(trifluoromethyl)benzamideHCID 15950818—

반응 조건

온도110 °C

반응 단계

A pressure tube was charged with N-methyl-9-vinyl-9H-purin-6-amine (0.088 g, 0.5 mmol), N-(3-iodo-4-methylphenyl)-3-(trifluoromethyl)benzamide (0.20 g, 0.5 mmol), palladium acetate (0.05 eq), tri-(o-tolyl)phosphine (0.1 eq), and DMF (2 ml). The resulting solution was degassed by bubbling N2 for 10 minutes. N,N-Diisopropylethylamine (0.19 g, 1.5 mmol) was added and this solution was stirred at 110° C. for 15 h. Water was added and the aqueous layer was extracted with ethyl acetate. The combined organic layers were dried over sodium sulfate, concentrated on a rotavap, and then subjected to silica gel column chromatography (5% methanol/methylene chloride) yielding the desired product: MS [M+H]+ 453; m.p. 201° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08071609B2
출처 데이터셋uspto-grants-2011_12
ORD IDord-cfddeecaa28b473484936fbc920a57e3
출처 메모uspto-grants-2011_12