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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 734650생성일: 2026년 10월 25일

1-Fluoro-3-isocyanato-5-(trifluoromethyl)benzene → 2-acetylamino-4-{4-[3-(3-fluoro-5-trifluoromethylphenyl)ureido]phenyl}-1H-pyrrole-3-carboxamide

https://huagongshe.com/reaction/734650

반응식

참여 물질

역할이름HCID투입량
반응물1-Fluoro-3-isocyanato-5-(trifluoromethyl)benzeneHCID 3445672—
반응물2-acetylamino-4-(4-aminophenyl)-1H-pyrrole-3-carboxamideHCID 69061860—
용매TetrahydrofuranHCID 8028—
생성물2-acetylamino-4-{4-[3-(3-fluoro-5-trifluoromethylphenyl)ureido]phenyl}-1H-pyrrole-3-carboxamideHCID 5784555141.8%

반응 단계

0.061 cm3 (0.426 mmol) of 3-fluoro-5-trifluoromethylphenyl isocyanate is added at room temperature to a suspension of 100 mg (0.387 mmol) of 2-acetylamino-4-(4-aminophenyl)-1H-pyrrole-3-carboxamide in 5 cm3 of anhydrous tetrahydrofuran. The reaction medium is stirred at room temperature for 24 hours, cooled in a water-ice bath and then filtered on sintered glass. The solid collected is washed with a small amount of dichloromethane and cyclohexane and then dried under vacuum. 75 mg of 2-acetylamino-4-{4-[3-(3-fluoro-5-trifluoromethylphenyl)ureido]phenyl}-1H-pyrrole-3-carboxamide are obtained in the form of a beige solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07592365B2
출처 데이터셋uspto-grants-2009_09
ORD IDord-4cd57cb910dd432b8625224f499fdc1c
출처 메모uspto-grants-2009_09