Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Cyanoacetamide | HCID 7898 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 7-chloro-3-methylthio-2H-1,4-benzothiazine | HCID 12871014 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 54553626 | HCID 54553626 | — |
Reaction Steps
To approximately 23 parts of sodium hydride in 4800 parts of N,N-dimethylformamide at room temperature under nitrogen is added, portionwise with stirring, 78 parts of 2-cyanoacetamide. Approximately 15 minutes later, a solution of 7-chloro-3-methylthio-2H-1,4-benzothiazine preparable as described in Part B of this example is slowly introduced, whereupon the reaction mixture is heated at 55° for 3 hours and then allowed to cool to room temperature overnight, stirring being continuous and the nitrogen atmosphere maintained throughout. The resultant mixture is acidified with glacial acetic acid and thereupon mixed with 3 volumes of water. Insoluble solids are filtered out and crystallized from aqueous N,N-dimethylformamide to give 2-cyano-2-(7-chloro-2,3-dihydro-4H-benzothiazin-3-ylidene)acetamide melting with decomposition in the range 150°-160°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04223136 |
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| Source dataset | uspto-grants-1980_09 |
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| ORD ID | ord-f60f60817928463b923dba023c53c265 |
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| Source note | uspto-grants-1980_09 |
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