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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 882822Generated: October 30, 2026

1,2-Dichloroethane → (2R)-N-(4-Amino-3,4-dioxo-1-phenylbutan-2-yl)-1-benzyl-5-oxopyrrolidine-2-carboxamide

https://huagongshe.com/reaction/882822

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
ReactantDichloroacetic AcidHCID 6597—
ReactantEthyl AcetateHCID 8857—
Reactant(2R)-N-(4-amino-3-hydroxy-4-oxo-1-phenylbutan-2-yl)-1-benzyl-5-oxopyrrolidine-2-carboxamideHCID 66644773—
SolventDimethyl SulfoxideHCID 679—
SolventWaterHCID 962—
Product(2R)-N-(4-Amino-3,4-dioxo-1-phenylbutan-2-yl)-1-benzyl-5-oxopyrrolidine-2-carboxamideHCID 67095000—

Reaction Conditions

Temperature5 °C

Reaction Steps

EDC (1543 mg, 8.05 mmol) and 2,2-dichloroacetic acid (0.446 ml; 696 mg, 5.4 mmol) were added to a solution of (2R)—N-(4-amino-3-hydroxy-4-oxo-1-phenylbutan-2-yl)-1-benzyl-5-oxopyrrolidine-2-carboxamide (400 mg, 1.012 mmol) in 8 ml of dry dimethylsulfoxide (DMSO), resulting in a slight exotheric reaction (40° C.). After stirring overnight at room temperature ethyl acetate and water were added, the formed precipitate filtered off and the remaining organic layer concentrated to dryness under reduced pressure. Precipitate and obtained residue were combined, and after addition of water and stirring at about 5° C. for 30 minutes the formed precipitate was filtered off and dried under reduced pressure. The title compound was obtained as an off-white powder (243 mg, yield: 61%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08236798B2
Source datasetuspto-grants-2012_08
ORD IDord-624b8da317df433aaa79ac38095b4468
Source noteuspto-grants-2012_08