HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diisopropylethylamine → N-(4-(6-Cyano-7-(2-methoxyethoxy)-4-quinolyl)oxyphenyl)-N'-(3-methylisoxazol-5-yl)urea
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 4-(4-Aminophenoxy)-6-cyano-7-(2-methoxyethoxy)quinoline | HCID 22936506 | — |
| Reactant | Phenyl (3-methylisoxazol-5-yl)carbamate | HCID 22936635 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | N-(4-(6-Cyano-7-(2-methoxyethoxy)-4-quinolyl)oxyphenyl)-N'-(3-methylisoxazol-5-yl)urea | HCID 22936702 | 74.5% |
Reaction Conditions
| Temperature | 100 °C |
|---|
Reaction Steps
The 4-(4-aminophenoxy)-6-cyano-7-(2-methoxyethoxy)quinoline (100 mg) synthesized in Production Example 10 and phenyl N-(3-methylisoxazol-5-yl)carbamate (81 mg) were added to toluene (5 ml), then diisopropylethylamine (0.88 ml) was added and the mixture was heated and stirred at 100° C. for 2 hours. After cooling, the precipitated crystals were filtered and washed with an ethyl acetate:toluene (1:1) mixed solvent to obtain the title compound (102 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07973160B2 |
| Source dataset | uspto-grants-2011_07 |
| ORD ID | ord-5e200d5030da45ca8fbfac8c2cca41ec |
| Source note | uspto-grants-2011_07 |