戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 415792作成日:2026年10月25日

4-(Trifluoromethyl)benzenecarbothioyl chloride → N-[2-(6-Bromo-2H-pyrazolo[4,3-b]pyridin-2-yl)-1-cyano-1-methylethyl]-4-trifluoromethylthiobenzamide

https://huagongshe.com/reaction/415792

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-bromo-2H-pyrazolo[4,3-b]pyridin-2-yl)-2-methylpropionitrileHCID 66620126—
生成物N-[2-(6-Bromo-2H-pyrazolo[4,3-b]pyridin-2-yl)-1-cyano-1-methylethyl]-4-trifluoromethylthiobenzamideHCID 86625600—

反応手順

Using a procedure similar to that described in Example 1, 2-amino-3-(6-bromo-2H-pyrazolo[4,3-b]pyridin-2-yl)-2-methylpropionitrile (223 mg described in Example 157) and 4-trifluoromethylthiobenzoyl chloride, the title compound was isolated as a white solid (145 mg, 38%). MS (ES): M/Z [M+H]=484. 1H NMR: (400 MHz, CHLOROFORM-d): 1.95 (s, 3H), 4.86 (d, J=14.0 Hz, 1H), 5.01 (d, J=14.1 Hz, 1H), 7.78 (d, J=8.3 Hz, 2H), 7.84-7.90 (m, 2H), 8.11 (s, 1H), 8.22 (dd, J=2.0, 1.0 Hz, 1H), 8.42 (d, J=0.8 Hz, 1H) and 8.64 (d, J=2.0 Hz, 1H). 19F NMR (376 MHz, CHLOROFORM-d): −42.2 (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-1dd9ce84d6df45ec8c4a145093e8bd4a
出典メモuspto-grants-2012_01