Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Ammonium Hydroxide | HCID 14923 | — |
| Reactant | HCID 20367572 | HCID 20367572 | — |
| Reactant | HCID 54329983 | HCID 54329983 | — |
| Product | HCID 54174205 | HCID 54174205 | — |
Reaction Steps
A mixture of 6.8 g of 1-methyl-3-(4-cyano-3-(ethylmethylamino)-5-isothiazolyl)urea and 20 ml of concentrated sulfuric acid was prepared by addition of small portions of the isothiazolylurea to the rapidly stirred sulfuric acid during a 15 minute period at ambient temperature. Stirring of the mixture was continued until a homogeneous solution was obtained. The solution was heated at 50° in a thermostated water bath for 1 hour. The reaction mixture was poured into 200 ml of ice-water and the resulting slurry was made strongly basic (pH 14) by addition of concentrated ammonium hydroxide. The temperature was maintained at 0° by addition of the ice during the pH adjustment process. The solid was collected by filtration and the filter cake dried. The solid was recrystallized from ethyl acetate to yield 4.4 g of 1-methyl-3-(4-carbamoyl-3-(ethylmethylamino)-5-isothiazolyl)urea, mp 165°-168°. The ir and nmr spectra were consistent with the assigned structure.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04075001 |
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| Source dataset | uspto-grants-1978_02 |
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| ORD ID | ord-f5cee3ae10df405a9c3858909ecf1924 |
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| Source note | uspto-grants-1978_02 |
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