Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methyl Isocyanate | HCID 12228 | — |
| Reactant | HCID 178473172 | HCID 178473172 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 21387492 | HCID 21387492 | — |
Reaction Steps
10 ml of methyl isocyanate were added to a solution of 11 g of 3-hydroxy-5-(ethoxycarbonylmethylthio)-1,2,4-thiadiazole in 100 ml of tetrahydrofuran containing 0.5 ml of triethylamine and the mixture was stirred for 2 hours at 20° C. The mixture was evaporated to dryness under reduced pressure and the residue was empasted with ethyl acetate and vacuum filtered. The crystals were washed with water to obtain 10 g of 2-(N-methylcarbamoyl)-5-(ethoxycarbonylmethylthio)-1,2,4-thiadiazole-3-one which after crystallization from acetone melted at 163° 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-8f76d5934f7146038079e6145e722c97 |
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| Source note | uspto-grants-1978_01 |
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