Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrogen Peroxide | HCID 784 | — |
| Reactant | HCID 18550870 | HCID 18550870 | — |
| Catalyst | Hydrogen Peroxide | HCID 784 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 21399274 | HCID 21399274 | — |
Reaction Steps
A mixture of 4.9 g of 1-methyl-3-(4-carbamoyl-3-(methylthio)-5-isothiazolyl)urea and 20 ml of acetic acid was heated to 95° and to the hot mixture was added dropwise 2.2 ml of 30% hydrogen peroxide. The mixture became homogeneous, but solid began to appear again after a few minutes. The mixture was maintained at 95° for two hours and then 9 drops of 30% hydrogen peroxide were added. After heating was continued an additional hour, thin-layer chromatographic analysis indicated that the reaction was completed. The mixture was cooled to -5°; the solid was isolated, washed with cold water and dried to give 4.7 g of 1-methyl-3-(4-carbamoyl-3-(methylsulfinyl)-5-isothiazolyl)urea; m.p. above 355°. The nmr spectrum was consistent with the assigned structure.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04057416 |
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| Source dataset | uspto-grants-1977_11 |
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| ORD ID | ord-7113d10369624685a6f94359e82104f1 |
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| Source note | uspto-grants-1977_11 |
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