戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1256958作成日:2026年10月25日

4-(Trifluoromethyl)benzenecarbothioyl chloride → N-[1-Cyano-2-(5,6-dichloro-2H-benzotriazol-2-yl)-1-methylethyl]-4-trifluoromethylthiobenzamide

https://huagongshe.com/reaction/1256958

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-(5,6-dichloro-2H-benzotriazol-2-yl)-2-methylpropionitrileHCID 66619862—
生成物N-[1-Cyano-2-(5,6-dichloro-2H-benzotriazol-2-yl)-1-methylethyl]-4-trifluoromethylthiobenzamideHCID 25122293—

反応手順

Using a procedure similar to that described in Example 1, except using 2-amino-3-(5,6-dichloro-2H-benzotriazol-2-yl)-2-methylpropionitrile, described in Example 13, and 4-trifluoromethylthiobenzoyl chloride, the title compound was isolated as a white solid (90 mg, 34%). MS (ES): M/Z [M+H]=474. 1H NMR: (400 MHz, DMSO-d6): 1.74 (s, 3H), 5.41-5.51 (m, 2H), 7.82-7.91 (m, 4H), 8.41 (br s, 2H) and 9.00 (s, 1H). 19F NMR (376 MHz, DMSO-d6): −41.94 (s, 3F).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08461176B2
出典データセットuspto-grants-2013_06
ORD IDord-20bdba24e6af4bdd81c7e5a3ef68ec73
出典メモuspto-grants-2013_06