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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 10525Generated: November 2, 2026

Hydrochloride methanol → 4-[(5-Isoquinolyl)oxy]piperidine hydrochloride

https://huagongshe.com/reaction/10525

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloride methanolHCID 21893726—
Reactant1-(Tert-butoxycarbonyl)-4-[(5-isoquinolyl)oxy]piperidineHCID 21979907—
Product4-[(5-Isoquinolyl)oxy]piperidine hydrochlorideHCID 21979801—

Reaction Steps

According to the method of Example 1, Step C, deprotection was performed (50° C., 2 hours) by using Intermediate 45 (164 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 (128 mg) as white powdery solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07094789B2
Source datasetuspto-grants-2006_08
ORD IDord-165bb2fd30774dcab9791f3bb61ece03
Source noteuspto-grants-2006_08