Potassium Iodide → HCID 57500748, compound

To a solution of 3H-thiopheno[2,3-d]1,2,3-triazin-4-one (80 mg, 0.522 mmol) in acetone (50 mL) was added sequentially potassium carbonate (144 mg, 1.04 mmol), iodomethane (0.04 mL, 0.627 mmol) and potassium iodide (catalytic) at rt and the mixture was stirred at rt for 3 h. The solution was filtered and the solids were washed with acetone. Acetone was evaporated under reduced pressure, diluted with ice cold water and stirred for 10 min. The solution was extracted with chloroform (4×75 mL) and the combined CHCl3 layer was washed with water, brine and dried over sodium sulfate. The solution was filtered and evaporated the solvent. The residue was chromatographed over silica gel column using hexane-ethyl acetate (90:10) as eluents to give the product as an off-white solid (50 mg, 57%), mp 104-108° C. 1H NMR (400 MHz, DMSO-d6): δ 8.17 (1H, d, J=5.6 Hz), 7.64 (1H, d, J=5.6 Hz), 3.95 (3H, s); 13C NMR (100 MHz, CDCl3): δ 159.4, 153.9, 130.7, 125.6, 121.7, 37.3.

1. filtrationThe solution was filtered
2. washthe solids were washed with acetone
3. customAcetone was evaporated under reduced pressure
4. additiondiluted with ice cold water
5. stirringstirred for 10 min
6. extractionThe solution was extracted with chloroform (4×75 mL)
7. washthe combined CHCl3 layer was washed with water, brine
8. dry with materialdried over sodium sulfate
9. filtrationThe solution was filtered
10. customevaporated the solvent
11. customThe residue was chromatographed over silica gel column

ORD record

ord-32a1e37896f547a1aa1d0fbc0e39bb90

Source dataset

uspto-grants-2012_09

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US08258119B2