Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Sodium Cyanate | HCID 517096 | — |
| Reactant | 1-methyl-4-ethoxycarbonylpyrazole-5-sulfonylchloride | HCID 10977963 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 19438397 | HCID 19438397 | 196.4% |
Reaction Steps
2.53 g (10 mmole) of 4-ethoxycarbonyl-1-methylpyrazole-5-sulfonylchloride was dissolved in 10.00 g of anhydrous acetonitrile. To the resulting solution was added dropwise 0.83 g (10.5 mmole) of dry pyridine over 5 minutes under nitrogen atmosphere by means of a syringe and the mixture was maintained at 40° C. To this mixture was added 0.72 g (11.0 mmole) of anhydrous sodium cyanate and the mixture was stirred while maintaining the temperature of 40° to 45° C. to complete the reaction. Then, the reaction mixture was treated according to the same procedure as Example 5 to obtain 3.50 g (Yield 90%) of the title compound as the white solid substance.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05534637 |
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| Source dataset | uspto-grants-1996_07 |
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| ORD ID | ord-c3f28d2363764b09b99a634df7ee2863 |
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| Source note | uspto-grants-1996_07 |
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