戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 415758作成日:2026年10月25日

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

https://huagongshe.com/reaction/415758

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-2-methyl-3-(5,7-dichloro-2H-indazol-2-yl)propionitrileHCID 66620022—
生成物N-[1-Cyano-2-(5,7-dichloro-2H-indazol-2-yl)-1-methylethyl]-4-trifluoromethylthiobenzamideHCID 86625575—

反応手順

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 98) 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).

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-f06cf1fa3d9b46feaf6de92b5d969baa
出典メモuspto-grants-2012_01