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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 573431Generated: October 31, 2026

N1-(6,7-Dimethoxyquinolin-4-yl)benzene-1,4-diamine → 3-(4-Fluorophenyl)-1-isopropyl-2,4-dioxo-1,2,3,4-tetrahydropyrimidine-5-carboxylic acid [4-(6,7-dimethoxyquinolin-4-ylamino)-phenyl]-amide

https://huagongshe.com/reaction/573431

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN1-(6,7-Dimethoxyquinolin-4-yl)benzene-1,4-diamineHCID 11197193—
Reactant3-(4-Fluorophenyl)-2,4-dioxo-1-(propan-2-yl)-1,2,3,4-tetrahydropyrimidine-5-carboxylic acidHCID 89581341—
Product3-(4-Fluorophenyl)-1-isopropyl-2,4-dioxo-1,2,3,4-tetrahydropyrimidine-5-carboxylic acid [4-(6,7-dimethoxyquinolin-4-ylamino)-phenyl]-amideHCID 90452697—

Reaction Steps

This compound was synthesized using N-(6,7-dimethoxyquinolin-4-yl)-benzene-1,4-diamine and 3-(4-fluorophenyl)-1-isopropyl-2,4-dioxo-1,2,3,4-tetrahydropyrimidine-5-carboxylic acid the method for example 134. mp=190-193° C.; LCMS m/z=570 (M+1); 1H NMR (DMSO-d6) δ: 10.85 (s, 1H), 8.65 (brs, 2H), 8.26 (d, 1H, J=5.3 Hz), 7.71 (d, 2H, J=8.8 Hz), 7.65 (s, 1H), 7.27-7.47 (m, 7H), 7.23 (s, 1H), 6.75 (d, 1H, J=5.3 Hz), 4.72-4.84 (m, 1H), 3.92 (s, 3H), 3.90 (s, 3H), 1.42 (d, 7H, J=6.8 Hz).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09029538B2
Source datasetuspto-grants-2015_05
ORD IDord-990f5c05a409480b89ca6c6ff66bdb45
Source noteuspto-grants-2015_05