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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 10510Generated: October 30, 2026

Hydrochloride methanol → N-(5-Isoquinolyl)-1,4-butylenediamine hydrochloride

https://huagongshe.com/reaction/10510

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloride methanolHCID 21893726—
Reactanttert-Butyl {4-[(isoquinolin-5-yl)amino]butyl}carbamateHCID 21979821—
ProductN-(5-Isoquinolyl)-1,4-butylenediamine hydrochlorideHCID 21979782—

Reaction Steps

According to the method of Example 1, Step C, deprotection was performed (50° C., 2 hours) by using Intermediate 30 (316 mg) and 10% hydrogen chloride/methanol solution (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 (1 ml) and diethyl ether (3 ml). The deposited precipitates were collected by filtration and washed with diethyl ether to obtain the title compound (276 mg) as light yellow powdery solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07094789B2
Source datasetuspto-grants-2006_08
ORD IDord-672a2fed6b53437e84c0e43685bb65b1
Source noteuspto-grants-2006_08