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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 17403생성일: 2026년 10월 24일

Triethylamine → 2-(Diethylamino)-7-fluoro-5-methyl-6-phenyl-1,3-benzoxazole-4-carbonitrile

https://huagongshe.com/ko/reaction/17403

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참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Sodium BicarbonateHCID 516892—
반응물Methylamine hydrochlorideHCID 6364545—
반응물2-Chloro-7-fluoro-5-methyl-6-phenyl-1,3-benzoxazole-4-carbonitrileHCID 51041429—
용매DichloromethaneHCID 6344—
생성물2-(Diethylamino)-7-fluoro-5-methyl-6-phenyl-1,3-benzoxazole-4-carbonitrileHCID 6858467282%

반응 조건

온도45 °C

반응 단계

2-Chloro-7-fluoro-5-methyl-6-phenyl-1,3-benzoxazole-4-cabonitrile (I-130) (100 mg, 0.35 mmol) was dissolved in dichloromethane (5 ml) in a sealed tube, then methylamine hydrochloride (26 mg, 0.38 mmol) and triethylamine (122 μl, 0.87 mmol) were successively added. The reaction system was heated at 45° C. for 3 hours. After cooling to room temperature, the reaction liquid was fractionated with dichloromethane and an aqueous saturated sodium hydrogencarbonate solution. The aqueous layer was separated, this was extracted twice with dichloromethane. The organic layers were combined, washed with saturated brine, then dried over anhydrous sodium sulfate. The insoluble matter was separated by filtration, the solvent was evaporated away, and the resulting residue was purified by preparative TLC (eluent, chloroform) to obtain the entitled compound (80 mg, 82%) as a white solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07737166B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-55af08ed1d3b45459730a9886818e8dd
출처 메모uspto-grants-2010_06