Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 10527Generated: October 25, 2026

Hydrochloride methanol → 4-(4-Bromo-5-isoquinolyl)aminopiperidine hydrochloride

https://huagongshe.com/reaction/10527

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloride methanolHCID 21893726—
Reactant4-(4-Bromo-5-isoquinolyl)amino-1-(tert-butoxycarbonyl)piperidineHCID 21979972—
Product4-(4-Bromo-5-isoquinolyl)aminopiperidine hydrochlorideHCID 21979908—

Reaction Steps

According to the method of Example 1, Step C, deprotection was performed (50° C., 2 hours) by using Intermediate 71 (123 mg) and 10% hydrogen chloride/methanol solution (6 ml). The reaction mixture was cooled to room temperature, and then the solvent was evaporated under reduced pressure. The residue was added with methanol (2 ml) and diethyl ether (6 ml). The deposited precipitates were collected by filtration and washed with diethyl ether to obtain the title compound (52 mg) as light yellow powdery solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07094789B2
Source datasetuspto-grants-2006_08
ORD IDord-c2cdce0bfcd242c092bbc9b6cdab22de
Source noteuspto-grants-2006_08