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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1028151Generated: October 27, 2026

Pyridine → 3-Benzyl-2,5-dioxoimidazolidine 1-hexylcarboxamide

https://huagongshe.com/reaction/1028151

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantHexyl isocyanateHCID 75659—
Reactant1-Benzylimidazolidine-2,4-dioneHCID 2735485—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventTolueneHCID 1140—
Product3-Benzyl-2,5-dioxoimidazolidine 1-hexylcarboxamideHCID 131731408—

Reaction Conditions

Temperature115 °C

Reaction Steps

1-Benzylimidazolidine-2,4-dione (100 mg, 0.526 mmol) and 1-isocyanatohexane (80.3 mg, 0.63 mmol) and, if required, a catalytic amount of 4-dimethylaminopyridine were dissolved in 10 ml of toluene and 0.5 ml of pyridine and stirred at 115° C. for 6 h. Then a further 80 mg of 1-isocyanatohexane were added, and the mixture was stirred at 115° C. for a further 6 h. The reaction mixture was concentrated and the residue was taken up in ethyl acetate and H2O, and the org. phases were washed twice with water, concentrated and purified by preparative HPLC (PR18, acetonitrile/water 0.1% TFA). Yield: 11.3 mg (7%), M+H+:318.14.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08735437B2
Source datasetuspto-grants-2014_05
ORD IDord-fe93801de6af459f8d4d780a3c9f400a
Source noteuspto-grants-2014_05