HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 703830Generated: October 27, 2026
Water → 2-benzylsulfonyl-6-methyl-5H-1,3,4-thiadiazolo[3,2-a]pyrimidin-5-one
https://huagongshe.com/reaction/703830
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | 2-benzylthio-6-methyl-5H-1,3,4-thiadiazolo[3,2-a]pyrimidin-5-one | HCID 14254420 | — |
| Reactant | Potassium hydroxy sulfite | HCID 23707502 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 2-benzylsulfonyl-6-methyl-5H-1,3,4-thiadiazolo[3,2-a]pyrimidin-5-one | HCID 15610912 | 52% |
Reaction Steps
In 75 ml of ethanol, 2.8 g of 2-benzylthio-6-methyl-5H-1,3,4-thiadiazolo[3,2-a]pyrimidin-5-one prepared in Preparation Example 1 was added and dissolved by warming the mixture to 60° C. To this solution, an aqueous suspension of 35.7 g OXONE ® of in 150 ml of water was added, and the mixture was stirred at 60° C. for 2 hours. After cooling, water was added to dissolve inorganic materials, and the deposited crystals were collected by filtration. The crystals were recrystallized from ethanol, and thus 1.6 g of 2-benzylsulfonyl-6-methyl-5H-1,3,4-thiadiazolo[3,2-a]pyrimidin-5-one was obtained. m.p. 171°-173° C. Yield 52%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04985432 |
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| Source dataset | uspto-grants-1991_01 |
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| ORD ID | ord-2318d268ac4c41b991d2bc05e98e2881 |
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| Source note | uspto-grants-1991_01 |
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