HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 387754Generated: October 26, 2026
Diisopropylethylamine → N-(4-(6-Cyano-7-(2-methoxyethoxy)-4-quinolyl)oxyphenyl)-N'-(3-methylisoxazol-5-yl)urea
https://huagongshe.com/reaction/387754
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 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), 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 |
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| Patent number | US08372981B2 |
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| Source dataset | uspto-grants-2013_02 |
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| ORD ID | ord-f4b10c5322fc41718a0334dc3943400a |
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| Source note | uspto-grants-2013_02 |
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