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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1786543Generated: October 25, 2026

1,2-Dichloroethane → (R)-N-(1-Benzyl-pyrrolidin-3-yl)-2-diphenylamino-N-methyl-acetamide

https://huagongshe.com/reaction/1786543

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
Reactant(Diphenylamino)acetic acidHCID 735138—
Reactant(R)-(1-benzoyl-pyrrolidin-3-yl)-methyl-amineHCID 70216545—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
Product(R)-N-(1-Benzyl-pyrrolidin-3-yl)-2-diphenylamino-N-methyl-acetamideHCID 57597569101.3%

Reaction Steps

To a solution of (R)-(1-benzoyl-pyrrolidin-3-yl)-methyl-amine(0.32 g, 1.68 mmol) in dry CH2Cl2 (20 ml) was added diphenylaminoacetic acid (0.38 g, 1.68 mmol) under nitrogen. To the reaction was added EDC (0.65 g, 3.36 mmol) and DMAP (cat) and the reaction mixture stirred under nitrogen at room temperature overnight. The reaction was then concentrated under reduced pressure. The residue was dissolved in ethyl acetate: water (10:1) (100 ml). The organic was washed with water (25 ml, 2×) and 10% NaOH (25 ml), dried over MgSO4 and evaporated to dryness. The resulting residue was purified by column chromatography using CH2Cl2:CH3OH (15:1) to give 0.68 g of desired product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07507760B2
Source datasetuspto-grants-2009_03
ORD IDord-fa9c619af59e4c759fc0932583cffe39
Source noteuspto-grants-2009_03