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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 352491Generated: October 30, 2026

Sodium Hydroxide → 4-(4-amino-2-butyl 1H-imidazo[4,5-c][1,5]naphthyridin-1-yl)butaneamine

https://huagongshe.com/reaction/352491

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
Reactant1,1-dimethylethyl N-[4-(4-amino-2-butyl-1H-imidazo[4,5-c][1,5]naphthyridin-1-yl)butyl]carbamateHCID 12112182—
SolventHydrochloric AcidHCID 313—
Product4-(4-amino-2-butyl 1H-imidazo[4,5-c][1,5]naphthyridin-1-yl)butaneamineHCID 1299261690.9%

Reaction Steps

A suspension of 1,1-dimethylethyl N-[4-(4-amino-2-butyl-1H-imidazo[4,5-c][1,5]naphthyridin-1-yl)butyl]carbamate (13.8 g) in 1N hydrochloric acid (140 mL) was heated on a steam bath for 1.5 hours. The reaction mixture was allowed to cool to ambient temperature and then it was made basic (pH>11) with 50% sodium hydroxide. The resulting precipitate was isolated by filtration, washed with water and then dried to provide 9.5 g of 4-(4-amino-2-butyl-1H-imidazo[4,5-c][1,5]naphthyridin-1-yl)butaneamine as a white solid, m.p. 212-213° C. Analysis: Calculated for C17H24N6: %C, 65.36; %H, 7.74; %N, 26.90; Found: %C, 65.16; %H, 7.65; %N, 27.29.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06747040B2
Source datasetuspto-grants-2004_06
ORD IDord-0ac64b9fc3ca4078bf0f1c0fca2d1b3d
Source noteuspto-grants-2004_06