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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 750373Generated: November 2, 2026

Tetrahydrofuran → HCID 10239853, compound

https://huagongshe.com/reaction/750373

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantPropanethioamideHCID 2760628—
ReactantHCID 23061001HCID 23061001—
SolventEthanolHCID 702—
ProductHCID 10239853HCID 1023985334.7%

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of 6-bromo-3-(2-bromoacetyl)-2-(4-methanesulfonylbenzyl)-4-phenyl-2H-isoquinolin-1-one (300 mg), thiopropionamide (70 mg), THF (3 ml) and ethanol (3 ml) was stirred at 80° C. for 12 hrs. The reaction mixture was concentrated under reduced pressure and saturated aqueous sodium hydrogen carbonate was added to the residue. The mixture was extracted with ethyl acetate. The organic layer was washed with water and saturated brine, and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (hexane:ethyl acetate=9:1-hexane:ethyl acetate=1:2) and recrystallized (ethyl acetate-hexane) to give the title compound (100 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07402595B2
Source datasetuspto-grants-2008_07
ORD IDord-315731f181574fc9a6c7aba3811ddab8
Source noteuspto-grants-2008_07