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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2236452Generated: November 1, 2026

Hydrochloric Acid → 6-cyclopentyl-4H-isoquinoline-1,3-dione

https://huagongshe.com/reaction/2236452

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantDiethyl EtherHCID 3283—
Reactant6-Bromo-1,3-bis-(tert-butyl-dimethyl-silanyloxy)-isoquinolineHCID 59300057—
ReactantHCID 178419650HCID 178419650—
CatalystHCID 178418397HCID 178418397—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product6-cyclopentyl-4H-isoquinoline-1,3-dioneHCID 42625831—

Reaction Steps

To 6-bromo-1,3-bis-(tert-butyl-dimethyl-silanyloxy)-isoquinoline (1.76 g, 3.75 mmole) is added tetrakis(triphenylphosphine)palladium (110 mg, 0.095 mmole) and 2M cyclopentyl magnesium bromide in ether (3.0 mL, 6.0 mmole). This mixture is heated using a microwave reactor at 75° C. for 600 sec. The mixture is cooled to room temperature, transferred to a flask with THF and water, then 2M hydrochloric acid (20 mL) is added and stirred for 4 hours at room temperature. The organic solvents were removed in vacuo, the mixture extracted with ethyl acetate, the organic layer dried over sodium sulfate filtered, evaporated and chromatographed with hexanes-ethyl acetate on silica gel to give a white solid, 268 mg (31%) MS (ESI): m/z 230.2 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07713994B2
Source datasetuspto-grants-2010_05
ORD IDord-ce4394cef63c46729cae2d156b479e39
Source noteuspto-grants-2010_05