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HRID 415715作成日:2026年10月27日

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

https://huagongshe.com/reaction/415715

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-(4,6-dichloro-2H-benzotriazol-2-yl)-2-methylpropionitrileHCID 66619910—
生成物N-[1-Cyano-2-(4,6-dichloro-2H-benzotriazol-2-yl)-1-methylethyl]-4-trifluoromethylthiobenzamideHCID 25122295—

反応手順

Using a procedure similar to that described in Example 1, except using 2-amino-3-(4,6-dichloro-2H-benzotriazol-2-yl)-2-methylpropionitrile, described in Example 15, and 4-trifluoromethylthiobenzoyl chloride, the title compound was isolated as a white solid (50 mg, 20%). Rf=0.7 (1:1 EA/heptane). MS (ES): M/Z [M+H]=475. NMR: (400 MHz, DMSO-d6): 1.75 (s, 3H), 5.40-5.56 (m, 2H), 7.65 (m, 1H), 7.79-7.95 (m, 4H), 8.10 (m, 1H) and 8.95 (s, 1H). 19F NMR (376 MHz, DMSO-d6): −42.05 (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-876fd60725a14276b2a7e9de21a4ca57
出典メモuspto-grants-2012_01