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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 47473Generated: October 29, 2026

HCID 22172708, compound → 6,7,8,9-tetrahydro-2-butyl-1-(2-methylpropyl)-1H-imidazo[4,5-c][1,5]naphthyridin-4-amine

https://huagongshe.com/reaction/47473

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 22172708HCID 22172708—
ReactantHCID 178418361HCID 178418361—
CatalystPlatinum oxide (PtO)HCID 82844—
SolventTrifluoroacetic acidHCID 6422—
Product6,7,8,9-tetrahydro-2-butyl-1-(2-methylpropyl)-1H-imidazo[4,5-c][1,5]naphthyridin-4-amineHCID 10214943—

Reaction Steps

A catalytic amount of platinum oxide was added to a solution of 2-butyl-1-(2-methylpropyl)-1H-imidazo[4,5-c][1,5]naphthyridin-4-amine (0.5 g) in trifluoroacetic acid (15 mL). The reaction mixture was reduced on a Parr apparatus under 50 psi (3.5 Kg/cm2) hydrogen pressure overnight. The reaction mixture was filtered to remove the catalyst and the filtrate was concentrated under vacuum. The residue was combined with aqueous sodium bicarbonate then a small amount of 10% sodium hydroxide was added. The resulting precipitate was extracted with dichloromethane. The dichloromethane extract was dried over magnesium sulfate then concentrated under vacuum. The residue was purified by flash chromatography (silica gel eluting with 1-5% methanol in dichloromethane containing 0.5% ammonium hydroxide). The eluant was concentrated under vacuum. The residue was recrystallized from hexane/ethyl acetate to provide 6,7,8,9-tetrahydro-2-butyl-1-(2-methylpropyl)-1H-imidazo[4,5-c][1,5]naphthyridin-4-amine as a solid, m.p. 143-147° C. Analysis: Calculated for C17H27N5: %C, 67.74; %H, 9.03; %N, 23.23. Found: %C, 61.90; %H, 7.51; %N, 19.91.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06699878B2
Source datasetuspto-grants-2004_03
ORD IDord-459d9bf0712a4c0e9f6a53a9f7d7e51e
Source noteuspto-grants-2004_03