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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 523783Generated: October 30, 2026

4-Benzyloxy-1-methoxy-isoquinoline-3-carboxylic acid butyl ester → 4-Hydroxy-1-methoxy-isoquinoline-3-carboxylic acid butyl ester

https://huagongshe.com/reaction/523783

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Benzyloxy-1-methoxy-isoquinoline-3-carboxylic acid butyl esterHCID 66712954—
CatalystPalladiumHCID 23938—
SolventEthyl AcetateHCID 8857—
Product4-Hydroxy-1-methoxy-isoquinoline-3-carboxylic acid butyl esterHCID 6671276492.8%

Reaction Steps

A mixture of 4-benzyloxy-1-methoxy-isoquinoline-3-carboxylic acid butyl ester (164 mg, 0.45 mmol), Pd/C (50 mg, 10 wt % Pd) and EtOAc (15 ml) was stirred under a H2-atmosphere at ambient pressure and temperature for 16 h. Then the mixture was filtered through a pad of celite. Celite and filter cake were washed thoroughly with EtOAc and the combined organic phases were concentrated in vacuo to give the title compound as a white solid (115 mg); 1H NMR (CDCl3): δ=11.48 (s, 1H), 8.27 to 8.32 (m, 1H), 8.17 to 8.21 (m, 1H), 7.65 to 7.78 (m, 2H), 4.43 (t, 2H), 4.10 (s, 3H), 1.87 (m, 2H), 1.54 (m, 2H), 1.02 (t, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09339527B2
Source datasetuspto-grants-2016_05
ORD IDord-0ccb4f8f22474935b35710bb9e7a157c
Source noteuspto-grants-2016_05