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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 10515Generated: October 30, 2026

Hydrochloride methanol → N-(Piperidin-3-ylmethyl)isoquinolin-5-amine hydrochloride

https://huagongshe.com/reaction/10515

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloride methanolHCID 21893726—
Reactant1-(Tert-butoxycarbonyl)-3-(5-isoquinolyl)aminomethylpiperidineHCID 21979926—
ProductN-(Piperidin-3-ylmethyl)isoquinolin-5-amine hydrochlorideHCID 21979978—

Reaction Steps

According to the method of Example 1, Step C, deprotection was performed (50° C., 2 hours) by using Intermediate 34 (171 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 (139 mg) as light yellow powdery solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07094789B2
Source datasetuspto-grants-2006_08
ORD IDord-919d2c5e1db54d07986b3c573f3147b2
Source noteuspto-grants-2006_08