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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1010139Generated: October 27, 2026

Diisopropylethylamine → N-(4-(6-Cyano-7-(2-methoxyethoxy)-4-quinolyl)oxyphenyl)-N'-(3-methylisoxazol-5-yl)urea

https://huagongshe.com/reaction/1010139

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant4-(4-Aminophenoxy)-6-cyano-7-(2-methoxyethoxy)quinolineHCID 22936506—
ReactantPhenyl (3-methylisoxazol-5-yl)carbamateHCID 22936635—
SolventTolueneHCID 1140—
ProductN-(4-(6-Cyano-7-(2-methoxyethoxy)-4-quinolyl)oxyphenyl)-N'-(3-methylisoxazol-5-yl)ureaHCID 2293670274.5%

Reaction Conditions

Temperature100 °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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07973160B2
Source datasetuspto-grants-2011_07
ORD IDord-5e200d5030da45ca8fbfac8c2cca41ec
Source noteuspto-grants-2011_07