戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 737002作成日:2026年10月26日

Triethylamine → 4-(3-Chloro-indazole-1-sulfonyl)-N-(4-fluoro-benzyl)-benzamide

https://huagongshe.com/reaction/737002

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物3-Chloro-1H-indazoleHCID 95894—
反応物4-(4-Fluoro-benzylcarbamoyl)-benzenesulfonyl chlorideHCID 58975125—
溶媒DichloromethaneHCID 6344—
生成物4-(3-Chloro-indazole-1-sulfonyl)-N-(4-fluoro-benzyl)-benzamideHCID 5897515283%

反応手順

Dissolve 3-chloro-1H-indazole (120 mg, 0.79 mmol) and 4-(4-fluoro-benzylcarbamoyl)-benzenesulfonyl chloride (114 mg, 0.35 mmol) in CH2Cl2 (2.0 mL) and treat with Et3N (50 L, 0.36 mmol). Stir the solution for 1 h at RT, then dilute with additional CH2Cl2 (20.0 mL) and wash with satd aq. NaHCO3 (15 mL). Dry, filter, and concentrate the organic phase and purify the crude material by flash chromatography (100% hexanes to 50% EtOAc/hexanes linear gradient) to give the title compound (129 mg, 83%) as a white foam. MS (ES+) 443.9 (M+1)+, (ES−) 442.0 (M−1)−. 1H NMR (400 MHz, CDCl3): δ 8.17 (d, 1H, J=8.3), 8.03 (d, 2H, J=8.2), 7.83 (d, 2H, J=8.9), 7.64 (m, 2H), 7.41 (t, 1H, J=7.4), 7.27 (m, 2H), 7.01 (t, 2H, J=8.9), 6.31 (br s, 1H), 4.57 (d, 2H, J=5.9).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07595339B2
出典データセットuspto-grants-2009_09
ORD IDord-7d1af9b7d86a421cbcdeaaa5266986a4
出典メモuspto-grants-2009_09