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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1698920Generated: October 31, 2026

4-Methylphenyl isocyanate → HCID 9858766, compound

https://huagongshe.com/reaction/1698920

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Methylphenyl isocyanateHCID 69325—
ReactantHCID 18322381HCID 18322381—
SolventTolueneHCID 1140—
ProductHCID 9858766HCID 985876640%

Reaction Steps

A solution of 2-amino-5-tert-butylthiophene-3-carboxamide (0.14 g, 0.7 mmol) and p-tolyl isocyanate (0.093 g, 0.7 mmol) in toluene (5 mL) was stirred at 60° C. overnight. The reaction mixture was separated between with water (10 mL) and EtOAc (10 mL). The aqueous phase was back-extracted with EtOAc (3×10 mL), and the combined organic phases were washed with a saturated NaCl solution (25 mL), dried (Na2SO4), and concentrated under reduced pressure. The residue was purified by chromatography (SiO2; gradient from 20% EtOAc/80% pet. ether to 30% EtOAc/70% pet ether) to give N-(3-carbamoyl-5-tert-butyl-2-thienyl)-N′-(4-methylphenyl)urea (0.092 g, 40%): 1H-NMR (CDCl3) δ1.38 (s, 9H), 2.32 (s, 3H), 5.58 (br s, 2H), 6.53 (s, 1H), 7.13 (app d, 2H), 7.35 (app d, 2H), 7.45 (br, 1H), 11.23 (br s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06344476B1
Source datasetuspto-grants-2002_02
ORD IDord-bb4714acbdb7431e91fab56c3e07b365
Source noteuspto-grants-2002_02