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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1186261Generated: October 26, 2026

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

https://huagongshe.com/reaction/1186261

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant1H-Indazol-6-amineHCID 81423—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Reactant3-(Benzenesulfonyl-benzyl-amino)-benzoic acidHCID 67310950—
ReactantHCID 178418395HCID 178418395—
SolventAcetonitrileHCID 6342—
Product3-(Benzenesulfonyl-benzyl-amino)-N-(1H-indazol-6-yl)-benzamideHCID 4618250545.7%

Reaction Steps

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).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08673901B2
Source datasetuspto-grants-2014_03
ORD IDord-c60bbf31b8c34f67bdea69ebb0b79f5b
Source noteuspto-grants-2014_03