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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1255419Generated: October 30, 2026

4-(1-Benzyloxy-7-chloro-isoquinolin-6-yloxy)-piperidine-1-carboxylic acid tert-butyl-ester → 7-Chloro-6-(piperidin-4-yloxy)-2h-isoquinolin-1-one-hydro-chloride

https://huagongshe.com/reaction/1255419

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(1-Benzyloxy-7-chloro-isoquinolin-6-yloxy)-piperidine-1-carboxylic acid tert-butyl-esterHCID 57652511—
SolventMethanolHCID 887—
Product7-Chloro-6-(piperidin-4-yloxy)-2h-isoquinolin-1-one-hydro-chlorideHCID 6745804269.6%

Reaction Steps

254 mg (0.52 mmol) of 4-(1-Benzyloxy-7-chloro-isoquinolin-6-yloxy)-piperidine-1-carboxylic acid tert-butyl-ester (6) were stirred in methanol/2 N HCl (1:1) at room temperature overnight. The solvent was removed i. vac. and the residue was purified by preparative HPLC. The product fractions were evaporated and dissolved in 2 N HCl. Lyophilization results in 57 mg of the desired compound. Rt=0.95 min (Method B). Detected mass: 279.1 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08461144B2
Source datasetuspto-grants-2013_06
ORD IDord-9ae281beaeb348bc98efa3f0dfc5890e
Source noteuspto-grants-2013_06