HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 750373Generated: November 2, 2026
Tetrahydrofuran → HCID 10239853, compound
https://huagongshe.com/reaction/750373
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Propanethioamide | HCID 2760628 | — |
| Reactant | HCID 23061001 | HCID 23061001 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 10239853 | HCID 10239853 | 34.7% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07402595B2 |
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| Source dataset | uspto-grants-2008_07 |
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| ORD ID | ord-315731f181574fc9a6c7aba3811ddab8 |
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| Source note | uspto-grants-2008_07 |
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