Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | ethyl N-carbonylcarbamate | HCID 300166 | — |
| Reactant | HCID 178467476 | HCID 178467476 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 21387500 | HCID 21387500 | 69% |
Reaction Steps
23 g of ethoxycarbonyl isocyanate were added dropwise to a solution of 14.6 g of 3-hydroxy-5-ethoxy-1,2,4-thiadiazole in 140 ml of tetrahydrofuran containing 1 ml of triethylamine and the mixture was stirred for 11/2 hours at 20° C and was filtered. The filtrate was concentrated to dryness and the residue was empasted with isopropyl ether and vacuum filtered. The product was crystallized from ethyl acetate to obtain 18 g of 2-(N-ethoxycarbonylcarbamoyl)-5-ethoxy-1,2,4-thiadiazole-3-one melting at 119° 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-c2ff21330bf944f3a6e175e2fd5bd7b5 |
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| Source note | uspto-grants-1978_01 |
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