HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 853276Generated: October 26, 2026
Diisopropylethylamine → N-(4-(6-Cyano-7-(2-methoxyethoxy)-4-quinolyl)oxyphenyl)-N'-(3-methylisoxazol-5-yl)urea
https://huagongshe.com/reaction/853276
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), 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 |
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| Patent number | US07253286B2 |
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| Source dataset | uspto-grants-2007_08 |
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| ORD ID | ord-8665f69db53c4a26a98a272ab4a84af0 |
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| Source note | uspto-grants-2007_08 |
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