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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2415701Generated: October 27, 2026

Triethylamine → N-(3-dimethylaminophenyl)-4-methyl-3-(5-methylisoxazol-3-ylcarbonylamino)benzamide

https://huagongshe.com/reaction/2415701

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant5-Methylisoxazole-3-carbonyl chlorideHCID 2736894—
Reactant3-amino-N-(3-dimethylaminophenyl)-4-methylbenzamideHCID 22636111—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
ProductN-(3-dimethylaminophenyl)-4-methyl-3-(5-methylisoxazol-3-ylcarbonylamino)benzamideHCID 2263616571.2%

Reaction Steps

Triethylamine (0.129 ml) was added to a stirred mixture of 3-amino-N-(3-dimethylaminophenyl)-4-methylbenzamide (0.1 g), 4-dimethylaminopyridine (5 mg), 5-methylisoxazol-3-ylcarbonyl chloride (0.081 g) and methylene chloride (3 ml) and the resultant mixture was stirred at ambient temperature for 16 hours. The mixture was diluted with methylene chloride (10 ml), washed with a saturated aqueous sodium bicarbonate solution and dried over magnesium sulphate. The organic solution was evaporated and the residue was triturated under isohexane. The resultant solid was dried at 55° C. under vacuum to give the title compound as a solid (0.1 g); NMR Spectrum: (CDCl3) 2.42 (s, 3H), 2.55 (s, 3H), 2.97 (s, 6H), 6.55 (m, 2H), 6.89 (d, 1H), 7.23 (m, 2H), 7.36 (d, 1H), 7.72 (d, 1H), 7.84 (broad s, 1H), 8.55 (broad s, 2H); Mass Spectrum: M+H+ 379.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06821965B1
Source datasetuspto-grants-2004_11
ORD IDord-1dbe069bd5de4d69adf54f322aebcb64
Source noteuspto-grants-2004_11