Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methyl Isocyanate | HCID 12228 | — |
| Reactant | HCID 178460815 | HCID 178460815 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 12526285 | HCID 12526285 | — |
Reaction Steps
0.5 ml of triethylamine and 5 ml of methyl isocyanate were added to a solution of 13.9 g of 3-hydroxy-5-allylthio-1,2,4-thiadiazole in 150 ml of tetrahydrofuran and the mixture was stirred at 20° C for 2 hours and was concentrated to dryness under reduced pressure. The residue was empasted with ethyl ether and was vacuum filtered and dried to obtain 15.9 g of 2-(N-methylcarbamoyl)-5-allylthio-1,2,4-thiadiazole-3-one melting at 110° 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-da390a74f497449495b39c641b55f716 |
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| Source note | uspto-grants-1978_01 |
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