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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

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), 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 numberUS08372981B2
Source datasetuspto-grants-2013_02
ORD IDord-f4b10c5322fc41718a0334dc3943400a
Source noteuspto-grants-2013_02