Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl Isocyanate | HCID 12228 | — |
| Reactant | HCID 178519016 | HCID 178519016 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 12526282 | HCID 12526282 | — |
Reaction Steps
5 ml of methyl isocyanate were added to a solution of 12.1 g of 3-hydroxy-5-(p-chlorobenzyloxy)-1,2,4-thiadiazole in 150 ml tetrahydrofuran and the mixture was stirred for 2 hours and 20° C and then concentrated to dryness. The residue was crystallized from ethyl acetate to obtain 7.3g of 2-(N-methylcarbamoyl)-5-(p-chlorobenzyloxy)-1,2,4-thiadiazole-3-one melting at 145° 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-7897ab07fd524bd4ba25f0b136fe9a69 |
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| Source note | uspto-grants-1978_01 |
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