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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 573441Generated: October 30, 2026

4-(6,7-Dimethoxyquinolin-4-yloxy)-2,3-difluoro-phenylamine → 1-Ethyl-3-(4-fluoro-phenyl)-2,4-dioxo-1,2,3,4-tetrahydro-pyrimidine-5-carboxylic acid [4-(6,7-dimethoxy-quinolin-4-yloxy)-2,3-difluoro-phenyl]-amide

https://huagongshe.com/reaction/573441

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(6,7-Dimethoxyquinolin-4-yloxy)-2,3-difluoro-phenylamineHCID 89580927—
Reactant1-Ethyl-3-(4-fluorophenyl)-2,4-dioxo-1,2,3,4-tetrahydropyrimidine-5-carboxylic acidHCID 89582618—
Product1-Ethyl-3-(4-fluoro-phenyl)-2,4-dioxo-1,2,3,4-tetrahydro-pyrimidine-5-carboxylic acid [4-(6,7-dimethoxy-quinolin-4-yloxy)-2,3-difluoro-phenyl]-amideHCID 90452706—

Reaction Steps

This compound was synthesized using 4-(6,7-dimethoxyquinolin-4-yloxy)-2,3-difluoro-phenylamine and 1-ethyl-3-(4-fluorophenyl)-2,4-dioxo-1,2,3,4-tetrahydropyrimidine-5-carboxylic acid using the procedure for example 1. mp=270-272° C.; LCMS m/z=593 (M+1); 1H NMR (CDCl3) δ: 11.08 (s, 1H), 8.63 (s, 1H), 5.51 (d, 1H, J=6 Hz), 8.28-8.22 (m, 1H), 7.55 (s, 1H), 7.43 (s, 1H), 7.25-7.23 (m, 4H), 7.09-7.03 (m, 1H), 6.46 (d, 1H, J=5 Hz), 4.05 (d, 6H), 4.04-3.99 (m, 2H), 1.47 (t, 3H, J=8 Hz).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09029538B2
Source datasetuspto-grants-2015_05
ORD IDord-584b6b6bf582411384229199d8d45e49
Source noteuspto-grants-2015_05