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HRID 415722作成日:2026年10月26日

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

https://huagongshe.com/reaction/415722

反応式

関与物質

役割名称HCID仕込み量
反応物4-(Trifluoromethyl)benzenecarbothioyl chlorideHCID 19862484—
反応物2-amino-3-(6-chloro-4-methyl-2H-benzotriazol-2-yl)-2-methylpropionitrileHCID 66620166—
生成物N-[2-(6-Chloro-4-methyl-2H-benzotriazol-2-yl)-1-cyano-1-methylethyl]-4-trifluoromethylthiobenzamideHCID 86625555—

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08088801B2
出典データセットuspto-grants-2012_01
ORD IDord-6bed32e43f214181b96942657209e63d
出典メモuspto-grants-2012_01