Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | HCID 14208916 | HCID 14208916 | — |
| Reactant | Potassium hydroxy sulfite | HCID 23707502 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 14100783 | HCID 14100783 | 49% |
Reaction Steps
In 240 ml of methanol, 6.3 g of 2-benzylthio-6-ethoxycarbonyl-5H-1,3,4-thiadiazolo[3,2-a]pyrimidin-5-one was dissolved. A suspension of 27.7 g of OXONE® dispersed in 110 ml of water was added to the methanol solution. The mixture was stirred at 60° C. for 2 hours, and was extracted with chloroform after cooling. The organic layer was washed with a sodium thiosulfate solution and water respectively and dried over anhydrous sodium sulfate. The solvent was distilled off. The residue was recrystallized from an acetonitrile/isopropylether (2:1) mixture and 3.3 g of 2-benzylsulfonyl-6-ethoxycarbonyl-5H-1,3,4-thiadiazolo[3,2-a]pyrimidin-5-one was obtained. m.p. 200°-203° C. Yield 49%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04742063 |
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| Source dataset | uspto-grants-1988_05 |
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| ORD ID | ord-4e010cde2b5244c8ab5f0db36b0a9d0d |
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| Source note | uspto-grants-1988_05 |
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