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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 70935생성일: 2026년 10월 25일

4-(Trifluoromethyl)benzenecarbothioyl chloride → N-[2-(6-Chloro-4-methyl-2H-benzotriazol-2-yl)-1-cyano-1-methylethyl]-4-trifluoromethylthiobenzamide

https://huagongshe.com/reaction/70935

반응식

참여 물질

역할이름HCID투입량
반응물4-(Trifluoromethyl)benzenecarbothioyl chlorideHCID 19862484—
반응물2-amino-3-(6-chloro-4-methyl-2H-benzotriazol-2-yl)-2-methylpropionitrileHCID 66620166—
생성물N-[2-(6-Chloro-4-methyl-2H-benzotriazol-2-yl)-1-cyano-1-methylethyl]-4-trifluoromethylthiobenzamideHCID 86625555—

반응 단계

Using a procedure similar to that described in Example 1, except using 2-amino-3-(6-chloro-4-methyl-2H-benzotriazol-2-yl)-2-methylpropionitrile, described in Example 27, and 4-trifluoromethylthiobenzoyl chloride, the title compound was isolated as a white solid (233 mg, 64%). MS (ES): M/Z [M+H]=454. NMR: (400 MHz, DMSO-d6): 1.74 (s, 3H), 2.47 (s, 3H), 5.44 (dd, J=57.5, 13.3 Hz, 2H), 7.27 (s, 1H), 7.79-7.99 (m, 5H) and 8.92 (s, 1H). 19F NMR (376 MHz, DMSO-d6): −42.01 (s, 3F).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08822689B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-439d7e5bc3924651ae616e20ce30f302
출처 메모uspto-grants-2014_09