HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 570939Generated: October 29, 2026
Potassium peroxymonosulphate → HCID 49868875, compound
https://huagongshe.com/reaction/570939
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium peroxymonosulphate | HCID 10313463 | — |
| Reactant | Potassium hydroxy sulfite | HCID 23707502 | — |
| Reactant | HCID 66831858 | HCID 66831858 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 49868875 | HCID 49868875 | 90% |
Reaction Steps
To a 0° C. solution of 3-(methylthiomethyl)-8-(5-phenyl-1,3,4-oxadiazol-2-yl)imidazo[5,1-d][1,2,3,5]tetrazin-4(3H)-one (0.337 mmol, 115 mg, 1 eq.) in DMF (6 mL) was added potassium peroxymonosulfate (Oxone™) (0.37 mmol, 114 mg, 1.1 eq.) dissolved in water (1.2 mL) drop wise. The formed suspension was stirred at 0° C. and stepwise additions of Oxone™ in water were made until reaction completion. The reaction mixture was filtered and the obtained solid was washed with water, acetonitrile and ether, and dried under vacuum to give the title compound. Yield 90%. δH (DMSO-d6) 9.15 (1H, s), 8.13 (2H, dd, J: 7.96, 2.25), 7.70 (3H, m), 5.67 (1H, d, J: 13.06), 5.52 (1H, d, J: 13.06), 2.81 (3H, s).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09024018B2 |
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| Source dataset | uspto-grants-2015_05 |
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| ORD ID | ord-73007035acc14c97abcfb0168ee76944 |
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| Source note | uspto-grants-2015_05 |
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