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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1930208Generated: November 2, 2026

Trifluoroacetic acid → 7-Methyl-6-(piperidin-4-yloxy)-2h-isoquinolin-1-one

https://huagongshe.com/reaction/1930208

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
Reactant4-[2-(4-Methoxy-benzyl)-7-methyl-1-oxo-1,2-dihydro-isoquinolin-6-yloxy]-piperidine-1-carboxylic acid tert-butyl esterHCID 67457974—
Product7-Methyl-6-(piperidin-4-yloxy)-2h-isoquinolin-1-oneHCID 57652508—

Reaction Conditions

Temperature150 °C

Reaction Steps

6.4 g (13.4 mmol) 4-[2-(4-methoxy-benzyl)-7-methyl-1-oxo-1,2-dihydro-isoquinolin-6-yloxy]-piperidine-1-carboxylic acid tert-butyl ester were dissolved in 30.5 g (267.4 mmol) trifluoroacetic acid. After 1 h at room temperature the mixture was heated for 2 h in a microwave oven at 150° C. Then the excess trifluoroacetic acid was distilled off in vacuo and the residue was diluted with 130 mL of 1 M hydrochloric acid. The aqueous phase was washed with methylene chloride 3 times and then it was freeze dried to give a hydrochloride, which was crystallized from isopropanol. This furnished 3.2 g 7-methyl-6-(piperidin-4-yloxy)-2H-isoquinolin-1-one (16) as hydrochloride.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08188117B2
Source datasetuspto-grants-2012_05
ORD IDord-2bba7191024246598a5620fc9cf6590e
Source noteuspto-grants-2012_05