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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 70936생성일: 2026년 10월 24일

4-Phenoxybenzoyl chloride → N-[2-(6-Chloro-4-methyl-2H-benzotriazol-2-yl)-1-cyano-1-methylethyl]-4-phenoxybenzamide

https://huagongshe.com/ko/reaction/70936

반응식

참여 물질

역할이름HCID투입량
반응물4-Phenoxybenzoyl chlorideHCID 74193—
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-phenoxybenzamideHCID 66620488—

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 (60 mg, described in Example 27) and 4-phenoxybenzoyl chloride (0.067 mL), the title compound was isolated as a white solid (90 mg, 84%). MS (ES): M/Z [M+H]=446. NMR: (400 MHz, DMSO-d6): 1.73 (s, 3H), 2.47 (s, 3H), 5.38 (d, J=13.3 Hz, 1H), 5.45 (d, J=13.3 Hz, 1H), 7.08 (t, J=8.25 Hz, 4H), 7.23 (t, 1H), 7.28 (s, 1H), 7.45 (t, 2H), 7.84 (d, J=8.79 Hz, 2H), 7.91 (m, 1H) and 8.68 (s, 1H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08822689B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-2e2b472f0601458a821796680bf36f47
출처 메모uspto-grants-2014_09