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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1713080Generated: November 1, 2026

6-(Benzyloxy)-2-[2-(4-cyclobutylpiperazin-1-yl)-2-oxoethyl]-1,2,3,4-tetrahydroisoquinoline → 2-[2-(4-Cyclobutylpiperazin-1-yl)-2-oxoethyl]-1,2,3,4-tetrahydroisoquinolin-6-ol

https://huagongshe.com/reaction/1713080

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6-(Benzyloxy)-2-[2-(4-cyclobutylpiperazin-1-yl)-2-oxoethyl]-1,2,3,4-tetrahydroisoquinolineHCID 57420564—
CatalystPalladium hydroxideHCID 9942167—
SolventEthanolHCID 702—
Product2-[2-(4-Cyclobutylpiperazin-1-yl)-2-oxoethyl]-1,2,3,4-tetrahydroisoquinolin-6-olHCID 57420696—

Reaction Steps

To a mixture of 6-(benzyloxy)-2-[2-(4-cyclobutylpiperazin-1-yl)-2-oxoethyl]-1,2,3,4-tetrahydroisoquinoline (2.5 g, 5.96 mmol) in EtOH (30 ml) is added 10% Pd(OH)2/C (0.5 g). The mixture is hydrogenated at 45 psi for 2 hr. The mixture is filtered through celite and washed with EtOH. The solvent is removed under reduced pressure to give the title compound. MS (+VE) m/z 330.2 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07795262B2
Source datasetuspto-grants-2010_09
ORD IDord-5ba63960bac84c3b8f805ffac644fa42
Source noteuspto-grants-2010_09