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HRID 1186261作成日:2026年10月25日

Triethylamine → 3-(Benzenesulfonyl-benzyl-amino)-N-(1H-indazol-6-yl)-benzamide

https://huagongshe.com/reaction/1186261

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物1H-Indazol-6-amineHCID 81423—
反応物1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
反応物3-(Benzenesulfonyl-benzyl-amino)-benzoic acidHCID 67310950—
反応物HCID 178418395HCID 178418395—
溶媒AcetonitrileHCID 6342—
生成物3-(Benzenesulfonyl-benzyl-amino)-N-(1H-indazol-6-yl)-benzamideHCID 4618250545.7%

反応手順

A solution of 3-(benzenesulfonyl-benzyl-amino)-benzoic acid (25 mg, 0.068 mmol), 6-amino-1H-indazole (18 mg, 0.136 mmol), 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (15 mg, 0.075 mmol), mercaptobenzothiazole (2 mg, 0.007 mmol) and triethylamine (24 μl, 0.17 mmol) in dry acetonitrile (2 ml) were stirred at room temperature for 15 hrs. The reaction mixture was quenched with water (10 ml) and extracted with dichloromethane (3×7 ml). The organics were combined, dried (PTFE frit) and concentrated in vacuo. The crude residue was purified by preparative TLC (10% diethyl ether in dichloromethane) to afford the title compound as a brown solid (15 mg, 45%). HPLC retention time 5.80 min. Mass spectrum (ES+) m/z 483 (M+H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08673901B2
出典データセットuspto-grants-2014_03
ORD IDord-c60bbf31b8c34f67bdea69ebb0b79f5b
出典メモuspto-grants-2014_03