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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 17476생성일: 2026년 10월 25일

Dichloromethane → 7-Fluoro-5-methyl-2-[methyl(pyridin-2-yl)amino]-6-phenyl-1,3-benzoxazole-4-carbonitrile

https://huagongshe.com/reaction/17476

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참여 물질

역할이름HCID투입량
반응물DichloromethaneHCID 6344—
반응물2-Pyridinamine, N-methyl-HCID 20727—
반응물DiisopropylethylamineHCID 81531—
반응물2-Chloro-7-fluoro-5-methyl-6-phenyl-1,3-benzoxazole-4-carbonitrileHCID 51041429—
용매Ethyl AcetateHCID 8857—
생성물7-Fluoro-5-methyl-2-[methyl(pyridin-2-yl)amino]-6-phenyl-1,3-benzoxazole-4-carbonitrileHCID 6858519257.7%

반응 조건

온도50 °C

반응 단계

Diisopropylethylamine (169 μl, 0.944 mmol) and 2-(methylamino)pyridine (102 μl, 0.994 mmol) were added to a dichloromethane (10 ml) solution of 2-chloro-7-fluoro-5-methyl-6-phenyl-1,3-benzoxazole-4-cabonitrile (I-130) (190 mg, 0.663 mmol), followed by heating under reflux in an oil bath at 50° C. for 3 hours. The reaction liquid was cooled to room, temperature, ethyl acetate (70 ml) was added, followed by washing with water (50 ml) and saturated brine (50 ml). After drying over anhydrous sodium sulfate and concentration under reduced pressure, the resulting residue was purified by silica gel column chromatography (eluent, hexane:ethyl acetate=4:1) to obtain the entitled compound (137 mg, 57.5%) as a colorless solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07737166B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-f1b148179b7e4b379a627f9581f4c5fc
출처 메모uspto-grants-2010_06