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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 10503Generated: October 26, 2026

Hydrochloride methanol → 3-[(1-Amino-5-isoquinolyl)oxy]propylamine hydrochloride

https://huagongshe.com/reaction/10503

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloride methanolHCID 21893726—
ReactantN-(tert-butoxycarbonyl)-3-[(1-amino-5-isoquinolyl)oxy]propylamineHCID 21979977—
Product3-[(1-Amino-5-isoquinolyl)oxy]propylamine hydrochlorideHCID 21979858—

Reaction Steps

According to the method of Example 1, Step C, deprotection was performed (50° C., 2 hours) by using Intermediate 20 (159 mg) and 10% hydrogen chloride/methanol solution (2.5 ml). The reaction mixture was cooled to room temperature, and then the solvent was evaporated under reduced pressure. The residue was added with methanol (0.5 ml) and diethyl ether (1.5 ml). The deposited precipitates were collected by filtration and washed with diethyl ether to obtain the title compound (116 mg) as white powdery solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07094789B2
Source datasetuspto-grants-2006_08
ORD IDord-40b53d9bfdf444818e70852330749f6c
Source noteuspto-grants-2006_08