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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1366763Generated: November 2, 2026

Trifluoroacetic acid → HCID 24782989, compound

https://huagongshe.com/reaction/1366763

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantPotassium CarbonateHCID 11430—
ReactantSodium BicarbonateHCID 516892—
Reactant6-hydroxyisoquinolin-1(2H)-oneHCID 10511170—
ReactantHCID 86618629HCID 86618629—
SolventMethanolHCID 887—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
ProductHCID 24782989HCID 24782989—

Reaction Conditions

Temperature90 °C

Reaction Steps

A solution of the methanesulfonic acid (1R,3S)-3-(tert-butoxycarbonyl-aminomethyl)cyclopentyl ester in N,N-dimethylformamide (2 ml) was added over 15 minutes to a stirred solution of 6-hydroxy-2H-isoquinolin-1-one (161 mg, 1 mmol) and potassium carbonate (276 mg) in N, N-dimethylformamide (2 ml) at 100° C. The mixture was stirred at 90° C. for 4 h then allowed to cool to ambient temperature and stirred overnight. Saturated aqueous NaHCO3 was added, the mixture was extracted with chloroform: isopropanol (3:1) and the organic phase concentrated in vacuo to give a residue. A dichloromethane: trifluoroacetic acid solution (3:1, 3 ml) was added to the residue and the resultant mixture stirred for 3.5 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 crude (1R,3S)-6-(3-aminomethylcyclopentyloxy)-2H-isoquinolin-1-one, which was purified by prep-HPLC (2 mg); EI-MS: m/z=259.1 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07893088B2
Source datasetuspto-grants-2011_02
ORD IDord-39a9d3f952fe4e9cb9700b924cf8e5c0
Source noteuspto-grants-2011_02