HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Cyclopropanecarbonyl chloride, 2-phenyl- → N-{4-[(6,7-Dimethoxy-4-quinolyl)oxy]phenyl}-N-ethyl-N'-[(2-phenylcyclopropyl)carbonyl]thiourea
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Cyclopropanecarbonyl chloride, 2-phenyl- | HCID 523092 | — |
| Edukt | 2-Phenyl-1-cyclopropanecarbonyl isothiocyanate | HCID 21890726 | — |
| Edukt | N-{4-[(6,7-Dimethoxy-4-quinolyl)oxy]phenyl}-N-ethylamine | HCID 21891226 | — |
| Lösungsmittel | Ethanol | HCID 702 | — |
| Lösungsmittel | Toluene | HCID 1140 | — |
| Produkt | 2-Phenyl-1-cyclopropanecarbonyl isothiocyanate | HCID 21890726 | — |
| Produkt | N-{4-[(6,7-Dimethoxy-4-quinolyl)oxy]phenyl}-N-ethyl-N'-[(2-phenylcyclopropyl)carbonyl]thiourea | HCID 72407261 | 53% |
Reaktionsschritte
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. N-{4-[(6,7-Dimethoxy-4-quinolyl)oxy]phenyl}-N-ethylamine (50 mg) was dissolved in toluene (5 ml) and ethanol (1 ml) to prepare a solution. A solution of 2-phenyl-1-cyclopropanecarbonyl isothiocyanate in ethanol (1 ml) was then 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 (43 mg, yield 53%).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US07135466B2 |
| Quelldatensatz | uspto-grants-2006_11 |
| ORD ID | ord-3fcea6a5dd0d4d86b507d1bd7d04d35a |
| Quellennotiz | uspto-grants-2006_11 |