HuagongsheHuagongshe Chemistry Print Report · For research reference only
Toluene → HCID 21890866, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Toluene | HCID 1140 | — |
| Reactant | 3-Cyclopentylpropionyl chloride | HCID 66039 | — |
| Reactant | 4-[(6,7-Dimethoxy-4-quinolyl)oxy]-2-chloroaniline | HCID 11221223 | — |
| Reactant | HCID 16775438 | HCID 16775438 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 16775438 | HCID 16775438 | — |
| Product | HCID 21890866 | HCID 21890866 | 41% |
Reaction Steps
3-Cyclopentylpropanoyl isothiocyanate was prepared using commercially available 3-cyclopentylpropanoyl chloride (80 mg) as a starting compound according to the description of the literature. 3-Cyclopentylpropanoyl isothiocyanate was dissolved in ethanol (1 ml) to prepare a solution. 2-Chloro-4-[(6,7-dimethoxy-4-quinolyl)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 (32 mg, yield 41%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07135466B2 |
| Source dataset | uspto-grants-2006_11 |
| ORD ID | ord-b44ca41416614829a19033950b7f8057 |
| Source note | uspto-grants-2006_11 |