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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1786560Generated: October 25, 2026

1,2-Dichloroethane → N-(1-Benzhydryl-2-oxo-pyrrolidin-3-yl)-2-diphenylamino-acetamide

https://huagongshe.com/reaction/1786560

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
Reactant(Diphenylamino)acetic acidHCID 735138—
Reactant3-Amino-1-benzhydryl-pyrrolidin-2-oneHCID 57597562—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
ProductN-(1-Benzhydryl-2-oxo-pyrrolidin-3-yl)-2-diphenylamino-acetamideHCID 5759756769%

Reaction Steps

To a solution of 3-amino-1-benzhydryl-pyrrolidin-2-one (42) (0.2 g, 0.75 mmol) in dry CH2Cl2 (20 ml)was added diphenylamino ethanoic acid (0.19 g, 0.82 mmol) under nitrogen. To the reaction was added EDC (0.18 g, 0.9 mmol) and DMAP (cat) and the reaction mixture was 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 hexane:ethyl acetate (2:1) to give the desired product in 69% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07507760B2
Source datasetuspto-grants-2009_03
ORD IDord-14563a3db8c14122aafee18220f7b5df
Source noteuspto-grants-2009_03