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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1436015Generated: October 31, 2026

Dimethylformamide → (S)-5-bromo-6-(piperidin-3-yloxy)-2H-isoquinolin-1-one

https://huagongshe.com/reaction/1436015

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantPotassium CarbonateHCID 11430—
Reactanttert-Butyl (3R)-3-[(methanesulfonyl)oxy]piperidine-1-carboxylateHCID 29939737—
Reactant5-bromo-6-hydroxy-2H-isoquinolin-1-oneHCID 68872858—
SolventMethanolHCID 887—
SolventWaterHCID 962—
Product(S)-5-bromo-6-(piperidin-3-yloxy)-2H-isoquinolin-1-oneHCID 16222775—

Reaction Steps

The crude 5-bromo-6-hydroxy-2H-isoquinolin-1-one (93 mg) was mixed with (R)-3-methanesulphonyloxypiperidine-1-carboxylic acid tert-butyl ester (500 mg, 4.3 mol eq), potassium carbonate (700 mg, 12 mol eq) and N, N-dimethylformamide (2 ml). The mixture was microwaved at 150° C. for 20 minutes. Water was added to the mixture and the crude product extracted out into ethyl acetate. The organic phase was washed with brine and dried (MgSO4). The organics were concentrated in vacuo then purified by prep-HPLC. Dichloromethane and trifluoroacetic acid (3:1, 2 ml) were added and the mixture stirred for 1 h then concentrated in vacuo to give a residue. The residue was loaded onto a pre-acidified SCX column using methanol and eluted with 2M ammonia in methanol to afford (S)-5-bromo-6-(piperidin-3-yloxy)-2H-isoquinolin-1-one. The residue was purified by prep-HPLC (1.8 mg), El-MS: m/z=323.5 and 323.5 [M+H]+

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07618985B2
Source datasetuspto-grants-2009_11
ORD IDord-11a88642b87e4abea619ebce4b3bb929
Source noteuspto-grants-2009_11