HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Ethylphenyl isocyanate → 2-Acetylamino-4-{4-[3-(3-ethylphenyl)ureido]phenyl}-1H-pyrrole-3-carboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Ethylphenyl isocyanate | HCID 2769637 | — |
| Reactant | 2-acetylamino-4-(4-aminophenyl)-1H-pyrrole-3-carboxamide | HCID 69061860 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-Acetylamino-4-{4-[3-(3-ethylphenyl)ureido]phenyl}-1H-pyrrole-3-carboxamide | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07592365B2 |
| Source dataset | uspto-grants-2009_09 |
| ORD ID | ord-d555e076b7cb4949bd1fc8122c71a0aa |
| Source note | uspto-grants-2009_09 |