Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisopropyl Ether | HCID 7914 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methyl Isocyanate | HCID 12228 | — |
| Reactant | HCID 178519019 | HCID 178519019 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 12526286 | HCID 12526286 | — |
Reaction Steps
0.2 ml of triethylamine and 6 ml of methyl isocyanate were added to a solution of 12.9 g of 3-hydroxy-5-(p-chlorobenzylthio)-1,2,4-thiadiazole in 100 ml of tetrahydrofuran and after stirring the mixture for 2 hours at 20° C, isopropyl ether was added thereto. The mixture was filtered and the crystals were empasted with isopropyl ether and dried to obtain 15 g of 2-(N-methylcarbamoyl)-5-(p-chlorobenzylthio)-1,2,4-thiadiazole-3-one melting at 140° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04067720 |
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| Source dataset | uspto-grants-1978_01 |
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| ORD ID | ord-9dc88e47f47841d493a95b82bf5cfeec |
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| Source note | uspto-grants-1978_01 |
|---|