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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 550889생성일: 2026년 10월 24일

2-Fluoro-5-(trifluoromethyl)phenyl isocyanate → 3-{4-[3-(2-fluoro-5-trifluoromethylphenyl)ureido]phenyl}-1H-pyrrolo[2,3-c]-pyridine-2-carboxamide

https://huagongshe.com/ko/reaction/550889

반응식

참여 물질

역할이름HCID투입량
반응물2-Fluoro-5-(trifluoromethyl)phenyl isocyanateHCID 2733380—
반응물3-(4-aminophenyl)-1H-pyrrolo[2,3-c]pyridine-2-carboxamideHCID 57445351—
용매DichloromethaneHCID 6344—
용매TetrahydrofuranHCID 8028—
생성물3-{4-[3-(2-fluoro-5-trifluoromethylphenyl)ureido]phenyl}-1H-pyrrolo[2,3-c]-pyridine-2-carboxamideHCID 16081737—

반응 단계

To a solution of 90 mg of 3-(4-aminophenyl)-1H-pyrrolo[2,3-c]pyridine-2-carboxamide in 5 mL of tetrahydrofuran are added dropwise 50 μL of 2-fluoro-5-(trifluoromethyl)phenyl isocyanate. The reaction mixture is stirred for 16 hours at room temperature under an argon atmosphere and then concentrated under reduced pressure. The residue obtained is stirred for 30 minutes in 2 mL of dichloromethane. The suspended solid is filtered off and drained by suction. After drying under vacuum, at 40° C., 115 mg of 3-{4-[3-(2-fluoro-5-trifluoromethylphenyl)ureido]phenyl}-1H-pyrrolo[2,3-c]-pyridine-2-carboxamide are obtained, the characteristics of which are as follows:

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07947706B2
출처 데이터셋uspto-grants-2011_05
ORD IDord-60c9fa15c9654d7bad5460c5118e8169
출처 메모uspto-grants-2011_05