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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 70928생성일: 2026년 10월 23일

4-(Trifluoromethyl)benzenecarbothioyl chloride → N-[1-Cyano-2-(4,6-dichloro-2H-benzotriazol-2-yl)-1-methylethyl]-4-trifluoromethylthiobenzamide

https://huagongshe.com/ko/reaction/70928

반응식

참여 물질

역할이름HCID투입량
반응물4-(Trifluoromethyl)benzenecarbothioyl chlorideHCID 19862484—
반응물2-Amino-3-(4,6-dichloro-2H-benzotriazol-2-yl)-2-methylpropionitrileHCID 66619910—
생성물N-[1-Cyano-2-(4,6-dichloro-2H-benzotriazol-2-yl)-1-methylethyl]-4-trifluoromethylthiobenzamideHCID 25122295—

반응 단계

Using a procedure similar to that described in Example 1, except using 2-amino-3-(4,6-dichloro-2H-benzotriazol-2-yl)-2-methylpropionitrile, described in Example 15, and 4-trifluoromethylthiobenzoyl chloride, the title compound was isolated as a white solid (50 mg, 20%). Rf=0.7 (1:1 EA/heptane). MS (ES): M/Z [M+H]=475. NMR: (400 MHz, DMSO-d6): 1.75 (s, 3H), 5.40-5.56 (m, 2H), 7.65 (m, 1H), 7.79-7.95 (m, 4H), 8.10 (m, 1H) and 8.95 (s, 1H). 19F NMR (376 MHz, DMSO-d6): −42.05 (s, 3F).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08822689B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-fbbe8b3d975c43da93f28066f74a5ee7
출처 메모uspto-grants-2014_09