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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 10504Generated: October 29, 2026

Hydrochloride methanol → 5-[(Piperidin-3-yl)methoxy]isoquinolin-1-amine--hydrogen chloride (1/1)

https://huagongshe.com/reaction/10504

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloride methanolHCID 21893726—
ReactantHCID 21979953HCID 21979953—
Product5-[(Piperidin-3-yl)methoxy]isoquinolin-1-amine--hydrogen chloride (1/1)HCID 21979843—

Reaction Steps

According to the method of Example 1, Step C, deprotection was performed (50° C., 2 hours) by using Intermediate 23 (179 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 (132 mg) as white powdery solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07094789B2
Source datasetuspto-grants-2006_08
ORD IDord-31ed84e073364a278a09080c0b0a2456
Source noteuspto-grants-2006_08