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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 602341Generated: October 30, 2026

Pyridine → 2-N-[(4-chlorophenyl)]-1-N-{[4-(3-oxomorpholin-4-yl)phenyl]}-(R)-pyrrolidine-1,2-dicarboxamide

https://huagongshe.com/reaction/602341

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantDiisopropylethylamineHCID 81531—
Reactant4-Nitrophenyl chloroformateHCID 82129—
Reactant4-(4-Aminophenyl)morpholin-3-oneHCID 11194854—
Reactant(R)-2-(4-chlorophenylcarbamoyl)pyrrolidinium chlorideHCID 86607080—
SolventDichloromethaneHCID 6344—
Product2-N-[(4-chlorophenyl)]-1-N-{[4-(3-oxomorpholin-4-yl)phenyl]}-(R)-pyrrolidine-1,2-dicarboxamideHCID 58691292—

Reaction Steps

1.01 g (5.00 mmol) of 4-nitrophenyl chloroformate and 0.404 ml (5.00 mmol) of pyridine are added to a solution of 961 mg (5.00 mmol) of 4-(4-aminophenyl)morpholin-3-one in 10 ml of dichloromethane, and the mixture is stirred at room temperature for 1 hour. 1.31 g (5.00 mmol) of (R)-2-(4-chlorophenylcarbamoyl)pyrrolidinium chloride and 2.55 ml (15.0 mmol) of N-ethyldiisopropylamine are added to the suspension. The reaction mixture is stirred at room temperature for 12 hours and then evaporated, and the residue is chromatographed on a silica-gel column, giving 2-N-[(4-chlorophenyl)]-1-N-{[4-(3-oxomorpholin-4-yl)phenyl]}-(R)-pyrrolidine-1,2-dicarboxamide as a yellowish solid, ESI 443.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07906516B2
Source datasetuspto-grants-2011_03
ORD IDord-ed081a49f55f4891b077586b2386f266
Source noteuspto-grants-2011_03