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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1034231Generated: October 31, 2026

Triethylamine → Ethyl cis-4-[[(3,4-dichlorophenyl)carbonyl]amino]-5-oxo-1-phenyl-3-pyrrolidinecarboxylate

https://huagongshe.com/reaction/1034231

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantBenzoyl chloride, 3,4-dichloro-HCID 76403—
ReactantEthyl 4-amino-5-oxo-1-phenyl-3-pyrrolidinecarboxylateHCID 19023548—
SolventDichloromethaneHCID 6344—
ProductEthyl cis-4-[[(3,4-dichlorophenyl)carbonyl]amino]-5-oxo-1-phenyl-3-pyrrolidinecarboxylateHCID 6779304367.3%

Reaction Steps

To a solution of 3,4-dichlorobenzoyl chloride (295 mg, 1.41 mmol) in CH2Cl2 (4 ml) was added a solution of aminopyrrolidinone of Example S (350 mg, 1.41 mmol) and triethylamine (0.4 ml, 2.82 mmol) in CH2Cl2 (4 ml) and the resulting solution was stirred for 18 h at room temperature. Concentration in vacuo gave an oil which was chromatographed on silica gel eluting with 2% EtOH/CH2Cl2 to give the title compound (400 mg, 67%) as a colorless solid. Anal calcd for C20H18N2O4Cl2 : C, 57.02; H, 4.31; N, 6.65. Found: C, 57.05; H, 4.39; N, 6.50. MS M+1 calcd for C20H18N2O4Cl2 422, found 422.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05314886
Source datasetuspto-grants-1994_05
ORD IDord-71f90f2264214e93bfb8ba94542848e6
Source noteuspto-grants-1994_05