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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 734651Generated: October 25, 2026

3-Ethylphenyl isocyanate → 2-Acetylamino-4-{4-[3-(3-ethylphenyl)ureido]phenyl}-1H-pyrrole-3-carboxamide

https://huagongshe.com/reaction/734651

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Ethylphenyl isocyanateHCID 2769637—
Reactant2-acetylamino-4-(4-aminophenyl)-1H-pyrrole-3-carboxamideHCID 69061860—
SolventTetrahydrofuranHCID 8028—
Product2-Acetylamino-4-{4-[3-(3-ethylphenyl)ureido]phenyl}-1H-pyrrole-3-carboxamideHCID 57845557—

Reaction Steps

0.061 cm3 (0.426 mmol) of 1-ethyl-3-isocyanatobenzene is added at room temperature to a suspension of 100 mg (0.387 mmol) of 2-acetylamino-4-(4-aminophenyl)-1H-pyrrole-3-carboxamide in 5 cm3 of anhydrous tetrahydrofuran. The reaction medium is stirred at room temperature for 24 hours and then evaporated to dryness under reduced pressure. The crude product is purified by flash chromatography [eluent; dichloromethane/methanol (97/3 by volume)]. After concentrating under reduced pressure the fractions containing the expected product, 107 mg of 2-acetylamino-4-{4-[3-(3-ethylphenyl)ureido]phenyl}-1H-pyrrole-3-carboxamide are obtained in the form of a brown solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07592365B2
Source datasetuspto-grants-2009_09
ORD IDord-d555e076b7cb4949bd1fc8122c71a0aa
Source noteuspto-grants-2009_09