HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1982167Generated: October 28, 2026
Water → 2-Benzyl-5-methoxy-2H-1,2,4,6-thiatriazin-3-one-1,1-dioxide
https://huagongshe.com/reaction/1982167
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | N-carbomethoxy-N'-benzylsulfamoyl-O-methylisourea | HCID 70392213 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-Benzyl-5-methoxy-2H-1,2,4,6-thiatriazin-3-one-1,1-dioxide | HCID 13645925 | — |
Reaction Steps
A solution of N-carbomethoxy-N'-benzylsulfamoyl-O-methylisourea (215 g) in anhydrous THF (200 ml) is added dropwise to a stirred suspension of sodium hydride (43 g of 60% dispersion) in anhydrous THF (900 ml) and refluxed for 2 hours under nitrogen. Water (800 ml) is added to the cooled reaction mixture and the aqueous mixture washed with ether. The pH of the aqueous layer is adjusted to about 3.2 and the resulting suspension extracted with methylene chloride. The methylene chloride extract is dried, filtered, and evaporated in vacuo. The residue is taken up in hot isopropyl alcohol, treated with charcoal, filtered hot, concentrated, cooled, the resulting precipitate filtered and dried in vacuo yielding the desired product, M.P.=141°-144° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04595683 |
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| Source dataset | uspto-grants-1986_06 |
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| ORD ID | ord-bc33fff268a8452f81cf63882f15fb39 |
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| Source note | uspto-grants-1986_06 |
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