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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1257006생성일: 2026년 10월 26일

4-(Trifluoromethyl)benzenecarbothioyl chloride → N-[1-Cyano-2-(5,7-dichloro-2H-indazol-2-yl)-1-methylethyl]-4-trifluoromethylthiobenzamide

https://huagongshe.com/reaction/1257006

반응식

참여 물질

역할이름HCID투입량
반응물4-(Trifluoromethyl)benzenecarbothioyl chlorideHCID 19862484—
반응물2-amino-2-methyl-3-(5,7-dichloro-2H-indazol-2-yl)propionitrileHCID 66620022—
생성물N-[1-Cyano-2-(5,7-dichloro-2H-indazol-2-yl)-1-methylethyl]-4-trifluoromethylthiobenzamideHCID 86625575—

반응 단계

Using a procedure similar to that described in Example 1, except using 2-amino-2-methyl-3-(5,7-dichloro-2H-indazol-2-yl)propionitrile (60 mg, described in Example 109) and 4-trifluoromethylthiobenzoyl chloride, the title compound was isolated as a white solid (80 mg, 76%). MS (ES): M/Z [M+H]=473. 1H NMR: (400 MHz, DMSO-d6): 1.70 (s, 3H), 5.11 (d, 1H), 5.25 (d, 1H), 7.48 (s, 1H), 7.84-7.91 (m, 3H), 7.95 (d, 2H), 8.54 (s, 1H) and 9.03 (s, 1H). 19F NMR (376 MHz, DMSO-d6): −42.0 (s, 3F).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08461176B2
출처 데이터셋uspto-grants-2013_06
ORD IDord-f38f50579d5c472ab24a57d4a6efa87f
출처 메모uspto-grants-2013_06