Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1930295Generated: October 25, 2026

1-(4-methoxyphenyl)-N-methylmethanamine → 7-((4-methoxybenzyl)(methyl)amino)-3-(5-amino-2,4-difluorophenyl)-1-methyl-1,6-naphthyridin-2(1H)-one

https://huagongshe.com/reaction/1930295

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(4-methoxyphenyl)-N-methylmethanamineHCID 485407—
Reactant3-(5-Amino-2,4-difluorophenyl)-7-chloro-1-methyl-1,6-naphthyridin-2(1H)-oneHCID 86620158—
Product7-((4-methoxybenzyl)(methyl)amino)-3-(5-amino-2,4-difluorophenyl)-1-methyl-1,6-naphthyridin-2(1H)-oneHCID 6909649691%

Reaction Conditions

Temperature200 °C

Reaction Steps

3-(5-Amino-2,4-difluorophenyl)-7-chloro-1-methyl-1,6-naphthyridin-2(1H)-one (2.4 g, 7.5 mmol) and 4-methoxy-N-methylbenzyl amine (10 mL) were combined in a sealed vessel and heated to 200° C. overnight. The volatiles were removed in vacuo and the residue was purified by column chromatography to give 7-((4-methoxybenzyl)(methyl)amino)-3-(5-amino-2,4-difluorophenyl)-1-methyl-1,6-naphthyridin-2(1H)-one (3 g, 91% yield), which was used in the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08188113B2
Source datasetuspto-grants-2012_05
ORD IDord-dcdc3bb095ff4010ad604cf983c7add7
Source noteuspto-grants-2012_05