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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 15100Generated: November 2, 2026

Pyrrolidine → N-acetyl-3-methyl-4-(pyrrolidin-1-yl-carbonyl)-aniline

https://huagongshe.com/reaction/15100

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyrrolidineHCID 31268—
ReactantOxalyl chlorideHCID 65578—
Reactant4-Acetamido-2-methylbenzoic acidHCID 2735224—
CatalystDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
ProductN-acetyl-3-methyl-4-(pyrrolidin-1-yl-carbonyl)-anilineHCID 68638637—

Reaction Conditions

Temperature50 °C

Reaction Steps

25.0 g (124 mmol) N-acetyl-4-amino-2-methyl-benzoic acid are combined with 3 drops DMF in 1000 ml dichloromethane and a solution of 21.0 ml (30.56 g, 241 mmol) oxalyl chloride in 100 ml TEA is added dropwise with stirring and cooling in the ice bath. Then the mixture is heated to 50° C. for 4.5 hours. The reaction mixture is filtered and the filtrate is evaporated down completely i. vac. The residue is taken up in 100 ml dichloromethane and this solution is added dropwise to a mixture of 10.4 ml (8.86 g, 125 mmol) pyrrolidine and 34.4 ml (25.0 g, 247 mmol) TEA in 500 ml dichloromethane with stirring and cooling in the ice bath. The mixture is stirred for 16 hours at ambient temperature. After filtering the filtrate is washed with 1-molar hydrochloric acid and sat. sodium chloride solution, combined with activated charcoal and dried over sodium sulphate. After evaporation i. vac. the residue is purified by chromatography on silica gel.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07732466B2
Source datasetuspto-grants-2010_06
ORD IDord-0a3ca745c61e42b585cbc2eb17bead3e
Source noteuspto-grants-2010_06