HuagongsheHuagongshe Chemistry Print Report · For research reference only
Toluene → N-{4-[(6,7-Dimethoxy-4-quinazolinyl)oxy]phenyl}-N'-[(2-phenylcyclopropyl)carbonyl]thiourea
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Toluene | HCID 1140 | — |
| Reactant | Cyclopropanecarbonyl chloride, 2-phenyl- | HCID 523092 | — |
| Reactant | 4-(6,7-Dimethoxyquinazolin-4-yloxy)aniline | HCID 11616363 | — |
| Reactant | 2-Phenyl-1-cyclopropanecarbonyl isothiocyanate | HCID 21890726 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | N-{4-[(6,7-Dimethoxy-4-quinazolinyl)oxy]phenyl}-N'-[(2-phenylcyclopropyl)carbonyl]thiourea | HCID 21889999 | 60% |
| Product | 2-Phenyl-1-cyclopropanecarbonyl isothiocyanate | HCID 21890726 | — |
Reaction Steps
2-Phenyl-1-cyclopropanecarbonyl isothiocyanate was prepared using commercially available 2-phenyl-1-cyclopropanecarbonyl chloride (80 mg) as a starting compound according to the description of the literature. 2-Phenyl-1-cyclopropanecarbonyl isothiocyanate was dissolved in ethanol (1 ml) to prepare a solution. 4-[(6,7-Dimethoxy-4-quinazolinyl)oxy]aniline (50 mg), toluene (5 ml), and ethanol (1 ml) were added to the solution, and the mixture was stirred at room temperature for 2 hr. The reaction solution was concentrated, and the residue was purified by chromatography on silica gel using chloroform/acetone for development to give the title compound (50 mg, yield 60%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07135466B2 |
| Source dataset | uspto-grants-2006_11 |
| ORD ID | ord-46996b4fe7294851b542b17dc7b2432a |
| Source note | uspto-grants-2006_11 |