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HRID 70940作成日:2026年10月23日

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

https://huagongshe.com/ja/reaction/70940

反応式

関与物質

役割名称HCID仕込み量
反応物4-Phenoxybenzoyl chlorideHCID 74193—
反応物2-amino-3-(6-chloro-4-trifluoromethyl-2H-benzotriazol-2-yl)-2-methylpropionitrileHCID 66620161—
生成物N-[2-(6-Chloro-4-trifluoromethyl-2H-benzotriazol-2-yl)-1-cyano-1-methylethyl]-4-phenoxybenzamideHCID 66620487—

反応手順

Using a procedure similar to that described in Example 1, except using 2-amino-3-(6-chloro-4-trifluoromethyl-2H-benzotriazol-2-yl)-2-methylpropionitrile (100 mg, described in Example 32) and 4-phenoxybenzoyl chloride (0.10 mL), the title compound was isolated as a white solid (95 mg, 58%). Rf=0.75 (1:1 EA/heptane). MS (ES): M/Z [M+H]=500. NMR: (400 MHz, DMSO-d6): 1.76 (s, 3H), 2.47 (s, 3H), 5.47 (d, J=13.3 Hz, 1H), 5.57 (d, J=13.3 Hz, 1H), 7.04-7.12 (m, 4H), 7.22 (t, J=7.4 Hz, 1H), 7.97 (s, 1H), 8.57 (s, 1H) and 8.69 (s, 1H). 19F NMR (376 MHz, DMSO-d6): −61.41 (s, 3F).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08822689B2
出典データセットuspto-grants-2014_09
ORD IDord-b9553a65c1f64ff8b1bf695b2795a665
出典メモuspto-grants-2014_09