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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 502032Generated: October 27, 2026

Triethylamine → 3-(4-carboxybenzamido)-N-(3-dimethylaminophenyl)-4-methylbenzamide

https://huagongshe.com/reaction/502032

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethyl 4-(chlorocarbonyl)benzoateHCID 81850—
Reactant3-amino-N-(3-dimethylaminophenyl)-4-methylbenzamideHCID 22636111—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
Product3-(4-carboxybenzamido)-N-(3-dimethylaminophenyl)-4-methylbenzamideHCID 9888202—

Reaction Steps

Triethylamine (0.26 ml) was added to a stirred mixture of 4-methoxycarbonylbenzoyl chloride (0.221 g), 4-dimethylaminopyridine (0.01 g), 3-amino-N-(3-dimethylaminophenyl)-4-methylbenzamide (0.2 g) and methylene chloride (10 ml) and the resultant mixture was stirred at ambient temperature for 16 hours. The mixture was diluted with methylene chloride and washed with a saturated aqueous sodium bicarbonate solution and with a saturated aqueous sodium chloride solution. The organic solution was dried over magnesium sulphate and evaporated. The residue was triturated under isohexane. The resultant solid was isolated and dried under vacuum at 55° C. to give the required starting material as a solid (0.286 g); NMR Spectrum: (CDCl3) 2.4 (s, 3H), 2.98 (s, 6H), 3.98 (s, 3H), 6.54 (m, 1H), 6.92 (d, 1H), 7.2 (m, 3H), 7.35 (d, 1H), 7.71 (d, 1H), 7.92 (s, 1H), 7.98 (d, 2H), 8.18 (d, 2H), 8.35 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07772432B2
Source datasetuspto-grants-2010_08
ORD IDord-f681111104dd4a75841821a4de28bea3
Source noteuspto-grants-2010_08