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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 10532Generated: October 26, 2026

Hydrochloride methanol → 4-Methyl-N-(piperidin-4-YL)isoquinolin-5-amine hydrochloride

https://huagongshe.com/reaction/10532

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloride methanolHCID 21893726—
Reactant4-(4-Methyl-5-isoquinolyl)amino-1-(tert-butoxycarbonyl)piperidineHCID 21979807—
Product4-Methyl-N-(piperidin-4-YL)isoquinolin-5-amine hydrochlorideHCID 21979810—

Reaction Steps

According to the method of Example 1, Step C, deprotection was performed (50° C., 2 hours) by using Intermediate 75 (90.7 mg) and 10% hydrogen chloride/methanol solution (2 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 (90.4 mg) as light yellow powdery solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07094789B2
Source datasetuspto-grants-2006_08
ORD IDord-b671ee9a0ae746f496e932de4e8b9c07
Source noteuspto-grants-2006_08