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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1057562Generated: November 3, 2026

N-(2-hydroxy-2-methylpropyl)-3-nitro[1,5]naphthyridin-4-amine → 1,1-Dimethyl-2-[(3-amino[1,5]naphthyridin-4-yl)amino]ethanol

https://huagongshe.com/reaction/1057562

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-(2-hydroxy-2-methylpropyl)-3-nitro[1,5]naphthyridin-4-amineHCID 22172695—
ReactantHCID 178418361HCID 178418361—
CatalystPlatinumHCID 23939—
SolventIsopropanolHCID 3776—
Product1,1-Dimethyl-2-[(3-amino[1,5]naphthyridin-4-yl)amino]ethanolHCID 22172687—

Reaction Steps

A catalytic amount of 5% platinum on carbon was added to a suspension of 1,1-dimethyl-2-[(3-nitro[1,5]naphthyridin-4-yl)amino]ethanol (7 g, 26 mmol) in isopropanol (300 mL). The mixture was hydrogenated on a Parr apparatus at 50 psi (3.5 Kg/cm2) hydrogen pressure for 3 hours. The reaction mixture was fileted to remove the catalyst. The filtrate was concentrated under vacuum. Toluene was added to the residue and the mixture was concentrated under vacuum to remove all of the alcohol and provide crude 1,1-dimethyl-2-[(3-amino[1,5]naphthyridin-4-yl)amino]ethanol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06514985B1
Source datasetuspto-grants-2003_02
ORD IDord-a7e8e99b2475496f9211363ce2ea5bbe
Source noteuspto-grants-2003_02