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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 570939Generated: October 29, 2026

Potassium peroxymonosulphate → HCID 49868875, compound

https://huagongshe.com/reaction/570939

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium peroxymonosulphateHCID 10313463—
ReactantPotassium hydroxy sulfiteHCID 23707502—
ReactantHCID 66831858HCID 66831858—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 49868875HCID 4986887590%

Reaction Conditions

Temperature0 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09024018B2
Source datasetuspto-grants-2015_05
ORD IDord-73007035acc14c97abcfb0168ee76944
Source noteuspto-grants-2015_05