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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 5434Generated: October 26, 2026

Hydrochloride methanol → 5-[3-(Amino)propylamino]imidazo[1,2-a]pyridine dihydrochloride

https://huagongshe.com/reaction/5434

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloride methanolHCID 21893726—
ReactantCarbamic acid,[3-(imidazo[1,2-a]pyridin-5-ylamino)propyl]-,1,1-dimethylethyl esterHCID 23362879—
SolventDichloromethaneHCID 6344—
Product5-[3-(Amino)propylamino]imidazo[1,2-a]pyridine dihydrochlorideHCID 2008666583%

Reaction Steps

To a suspension of 5-[3-(tert-butoxycarbonylamino)propylamino]imidazo[1,2-a]pyridine (1.742 g, 6 mmoles) in methylene chloride (40 ml) was added hydrogen chloride-methanol (6 ml) and the mixture was stirred at room temperature for 20 hours. After the solvent was distilled off, ethanol (15 ml) and ether (30 ml) were added to the residue. Then, the crystals precipitated were filtered off and washed in turn with ether and a small amount of ethanol to obtain 1.311 g of the desired product (83.0%, pale yellow crystals).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05244908
Source datasetuspto-grants-1993_09
ORD IDord-689b4b2ef67943d4b073104bea7fe4b7
Source noteuspto-grants-1993_09