Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2050348Generated: October 30, 2026

Dicyclohexylcarbodiimide → (2,4-Dioxo-5-methyl-1-propargyl-3-imidazolidinyl)methyl 2-(2-chloro-4-trifluoromethylphenylamino)-3-methylbutanoate

https://huagongshe.com/reaction/2050348

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDicyclohexylcarbodiimideHCID 10868—
Reactant2-DimethylaminopyridineHCID 21885—
ReactantL-Valine, N-[2-chloro-4-(trifluoromethyl)phenyl]-HCID 156536—
Reactant(2,4-Dioxo-5-methyl-1-propargyl-3-imidazolidinyl)methanolHCID 20342664—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
Product(2,4-Dioxo-5-methyl-1-propargyl-3-imidazolidinyl)methyl 2-(2-chloro-4-trifluoromethylphenylamino)-3-methylbutanoateHCID 20342656—

Reaction Steps

To a stirred solution of (2,4-dioxo-5-methyl-1-propargyl-3-imidazolidinyl)methanol (1.8 mmol), N-(2-chloro-4-trifluoromethylphenyl)valine (2.0 mmol) and dimethylaminopyridine (0.65 mmol) in 20 ml of methylene chloride and 2 ml of dimethylformamide is added N,N'-dicyclohexylcarbodiimide (2.0 mmol). The reaction mixture is stirred, under nitrogen, for two hours and then filtered and extracted with water. The aqueous phase is extracted with ether. The combined organic phases are washed with saturated aqueous sodium bicarbonate, water and saturated aqueous sodium chloride, dried over calcium sulfate and solvent evaporated. The crude product is chromatographed on a rotary chromatograph, eluting with 25% ether/hexane, to yield (2,4-dioxo-5-methyl-1-propargyl-3-imidazolidinyl)methyl 2-(2-chloro-4-trifluoromethylphenylamino)-3-methylbutanoate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04200758
Source datasetuspto-grants-1980_04
ORD IDord-9f808152bce54c8a8b2825ebae58721a
Source noteuspto-grants-1980_04