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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 256364Generated: October 25, 2026

Triethylamine → 2,2-Dimethyl-5-oxo-3-(2-oxo-1-pyrrolidineacetyl)-1-imidazolidineacetamide

https://huagongshe.com/reaction/256364

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantButyl chloroformateHCID 61140—
Reactant2-(2-Oxopyrrolidin-1-yl)acetic acidHCID 3146687—
Reactant2,2-Dimethyl-5-oxo-1-imidazolidineacetamideHCID 20155466—
SolventDimethylformamideHCID 6228—
Product2,2-Dimethyl-5-oxo-3-(2-oxo-1-pyrrolidineacetyl)-1-imidazolidineacetamideHCID 20163709—

Reaction Conditions

Temperature0 °C

Reaction Steps

An ice cold solution of 2-oxo-1-pyrrolidineacetic acid (1.45 g) and triethylamine (1.45 ml) in dimethylformamide (7 ml) was treated dropwise while stirring with butyl chloroformate (1.3 ml). After stirring at 0° C. for 45 minutes, 2,2-dimethyl-5-oxo-1-imidazolidineacetamide (1.75 g) was added at once and stirring was prolonged at room temperature overnight. After evaporation under reduced pressure, the residue was chromatographed on a silica gel column, eluting with dichloromethane/methanol 1:1. The selected fractions were collected and evaporated, the residue was taken up with ethyl acetate and the resulting solid was crystallized from ethanol, to give the title compound as a white powder, m.p. 225°-227° C., (decomp.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04703054
Source datasetuspto-grants-1987_10
ORD IDord-8bd97c6e19a4404ca2ced4eba6826bdc
Source noteuspto-grants-1987_10