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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2274212Generated: October 26, 2026

2-Nitroaniline → 3-(3,5-dimethoxyphenyl)-1,8-dimethyl-7-(2-nitrophenylamino)-1,6-naphthyridin-2(1H)-one

https://huagongshe.com/reaction/2274212

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-NitroanilineHCID 6946—
ReactantPotassium tert-butoxideHCID 23665647—
Reactant7-chloro-3-(3,5-dimethoxyphenyl)-1,8-dimethyl-1,6-naphthyridin-2(1H)-oneHCID 86713591—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventDimethylformamideHCID 6228—
Product3-(3,5-dimethoxyphenyl)-1,8-dimethyl-7-(2-nitrophenylamino)-1,6-naphthyridin-2(1H)-oneHCID 8671359215%

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of 7-chloro-3-(3,5-dimethoxyphenyl)-1,8-dimethyl-1,6-naphthyridin-2(1H)-one (800 mg, 2.32 mmol), 2-nitrobenzenamine (320 mg, 2.32 mmol), Pd2(dba)3 (100 mg), John-Phos (100 mg) and potassium tert-butanolate (480 mg, 4.64 mmol) in N,N-dimethylformamide (10 mL) was heated in sealed tube at 100° C. under microwave for 1 h. LCMS monitored the reaction was completed. The mixture was concentrated and purified by Prep-HPLC to get the title compound (150 mg, 15%) as a brown solid. MS (ES+) C24H22N4O5 requires: 446. Found: 447 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09126951B2
Source datasetuspto-grants-2015_09
ORD IDord-5ac9e45a1a78421096a7745b10f252d5
Source noteuspto-grants-2015_09