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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 71005생성일: 2026년 10월 24일

4-(Trifluoromethyl)benzenecarbothioyl chloride → N-[2-(6-Bromo-2H-pyrazolo[4,3-b]pyridin-2-yl)-1-cyano-1-methylethyl]-4-trifluoromethylthiobenzamide

https://huagongshe.com/ko/reaction/71005

반응식

참여 물질

역할이름HCID투입량
반응물4-(Trifluoromethyl)benzenecarbothioyl chlorideHCID 19862484—
반응물2-Amino-3-(6-bromo-2H-pyrazolo[4,3-b]pyridin-2-yl)-2-methylpropionitrileHCID 66620126—
생성물N-[2-(6-Bromo-2H-pyrazolo[4,3-b]pyridin-2-yl)-1-cyano-1-methylethyl]-4-trifluoromethylthiobenzamideHCID 86625600—

반응 단계

Using a procedure similar to that described in Example 1, 2-amino-3-(6-bromo-2H-pyrazolo[4,3-b]pyridin-2-yl)-2-methylpropionitrile (223 mg described in Example 157) and 4-trifluoromethylthiobenzoyl chloride, the title compound was isolated as a white solid (145 mg, 38%). MS (ES): M/Z [M+H]=484. 1H NMR: (400 MHz, CHLOROFORM-d): 1.95 (s, 3H), 4.86 (d, J=14.0 Hz, 1H), 5.01 (d, J=14.1 Hz, 1H), 7.78 (d, J=8.3 Hz, 2H), 7.84-7.90 (m, 2H), 8.11 (s, 1H), 8.22 (dd, J=2.0, 1.0 Hz, 1H), 8.42 (d, J=0.8 Hz, 1H) and 8.64 (d, J=2.0 Hz, 1H). 19F NMR (376 MHz, CHLOROFORM-d): −42.2 (s, 3F).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08822689B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-1703c352cb704d2d8f974672e72b98ba
출처 메모uspto-grants-2014_09