HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1698920Generated: October 31, 2026
4-Methylphenyl isocyanate → HCID 9858766, compound
https://huagongshe.com/reaction/1698920
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Methylphenyl isocyanate | HCID 69325 | — |
| Reactant | HCID 18322381 | HCID 18322381 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 9858766 | HCID 9858766 | 40% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06344476B1 |
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| Source dataset | uspto-grants-2002_02 |
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| ORD ID | ord-bb4714acbdb7431e91fab56c3e07b365 |
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| Source note | uspto-grants-2002_02 |
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