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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1186261생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/1186261

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물1H-Indazol-6-amineHCID 81423—
반응물1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
반응물3-(Benzenesulfonyl-benzyl-amino)-benzoic acidHCID 67310950—
반응물HCID 178418395HCID 178418395—
용매AcetonitrileHCID 6342—
생성물3-(Benzenesulfonyl-benzyl-amino)-N-(1H-indazol-6-yl)-benzamideHCID 4618250545.7%

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08673901B2
출처 데이터셋uspto-grants-2014_03
ORD IDord-c60bbf31b8c34f67bdea69ebb0b79f5b
출처 메모uspto-grants-2014_03