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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 230554생성일: 2026년 10월 24일

2-Fluoro-5-methylphenyl isocyanate → 4-[3-(2-Fluoro-5-methylphenyl)ureidophenyl]-1H-indole-2-carboxamide

https://huagongshe.com/ko/reaction/230554

반응식

참여 물질

역할이름HCID투입량
반응물2-Fluoro-5-methylphenyl isocyanateHCID 2733377—
반응물3-(4-Aminophenyl)-1H-indole-2-carboxamideHCID 57762833—
용매TetrahydrofuranHCID 8028—
생성물4-[3-(2-Fluoro-5-methylphenyl)ureidophenyl]-1H-indole-2-carboxamideHCID 68827944226.9%

반응 조건

온도20 °C

반응 단계

0.115 cm3 (0.876 mmol) of 2-fluoro-5-methylphenyl isocyanate is added, at a temperature in the region of 20° C., under an argon atmosphere, to 0.2 g (0.796 mmol) of 3-(4-aminophenyl)-1H-indole-2-carboxamide in solution in 10 cm3 of tetrahydrofuran. After stirring for 18 hours at a temperature in the region of 20° C., the reaction mixture is concentrated to dryness under reduced pressure (2.7 kPa), to give 400 mg of a residue which is purified by flash chromatography [eluent: ethyl acetate/cyclohexane (7/3 by volume)]. After concentration under reduced pressure of the fractions containing the expected product, 250 mg of a yellow residue are obtained, which residue is stirred in 10 cm3 of dichloromethane and then filtered and dried under reduced pressure (2.7 kPa), to give 180 mg of 3-{4-[3-(2-fluoro-5-methylphenyl)ureido]phenyl}-1H-indole-2-carboxamide, in the form of a beige solid that melts at 220° C.;

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07566736B2
출처 데이터셋uspto-grants-2009_07
ORD IDord-bacf64b2350944daa124f842c48100cb
출처 메모uspto-grants-2009_07