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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1081639Generated: October 26, 2026

Guanidine Hydrochloride → 2,4,6-Triamino-5-[3-(naphth-1-yl)propyl]pyrimidine

https://huagongshe.com/reaction/1081639

Reaction equation

Participants

RoleNameHCIDCharge
ReactantGuanidine HydrochlorideHCID 5742—
ReactantSodium ethoxideHCID 2723922—
ReactantSodiumHCID 5360545—
Reactant2-Cyano-5-(naphth-1-yl)pentanenitrileHCID 19955544—
SolventEthanolHCID 702—
Product2,4,6-Triamino-5-[3-(naphth-1-yl)propyl]pyrimidineHCID 19955501—

Reaction Steps

A solution of sodium ethoxide, prepared from 0.04: gram (0.002 mole) of sodium metal in 50 mL of ethanol, was stirred, and 0.2 gram (0.002 mole) of guanidine hydrochloride was added in one portion. The reaction mixture was stirred for 15 minutes and filtered to remove a precipitate. The filtrate was stirred, and 0.4 gram (0.002 mole) of 2-cyano-5-(naphth-1-yl)pentanenitrile was added in one portion. Upon completion of addition, the reaction mixture was heated at reflux for about 16 hours. After this time the reaction mixture was concentrated under reduced pressure to a residue. The residue was triturated with warm water, yielding, when dried, 0.4 gram of 2,4,6-triamino-5-[3-(naphth-1-yl)propyl]-pyrimidine, mp 181°-183° C., (dec.). The NMR spectrum was consistent with the proposed structure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05587379
Source datasetuspto-grants-1996_12
ORD IDord-2fc511b73fdf4e8283cdd24ced3f170e
Source noteuspto-grants-1996_12