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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 573457Generated: October 31, 2026

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

https://huagongshe.com/reaction/573457

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(6,7-Dimethoxy-quinolin-4-yloxy)-3-trifluoromethyl-phenylamineHCID 89581567—
Reactant2-Ethyl-4-(4-fluoro-phenyl)-3,5-dioxo-2,3,4,5-tetrahydro-1,2,4-triazine-6-carboxylic acidHCID 89581572—
Product2-Ethyl-4-(4-fluoro-phenyl)-3,5-dioxo-2,3,4,5-tetrahydro-1,2,4-triazine-6-carboxylic acid [4-(6,7-dimethoxy-quinolin-4-yloxy)-3-trifluoromethyl-phenyl]-amideHCID 90452724—

Reaction Steps

This compound was synthesized using 4-(6,7-dimethoxy-quinolin-4-yloxy)-3-trifluoromethyl-phenylamine and 2-ethyl-4-(4-fluoro-phenyl)-3,5-dioxo-2,3,4,5-tetrahydro-1,2,4-triazine-6-carboxylic acid using the procedure for example 1. mp=148-50° C.; LCMS m/z=626 (M+1); 1H NMR (DMSO): 10.95 (s, 1H), 8.52 (d, 1H), 8.32 (s, 1H), 8.04 (m, 1H), 7.35-7.49 (m, 8H), 6.60 (m, 1H), 4.08 (q, 2H, J=7Hz), 3.97 (s, 3H), 3.89 (s, 3H), 1.35 (t, 3H, J=7Hz).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09029538B2
Source datasetuspto-grants-2015_05
ORD IDord-602d979820464821b2419d68d3e96a72
Source noteuspto-grants-2015_05