Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Cyanate | HCID 517096 | — |
| Reactant | 4-Methoxy-6-methylpyrimidin-2-amine | HCID 587236 | — |
| Reactant | HCID 13364388 | HCID 13364388 | — |
| Catalyst | Pyridine | HCID 1049 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 19438399 | HCID 19438399 | 108.3% |
Reaction Steps
23.8 g of 4-methoxycarbonyl-1-methylpyrazole-5-sulfonamide was dissolved in 100 g of acetonitrile and 8.0 g of sodium cyanate and 13.9 g of 2-amino-4-methoxy-6-methylpyrimidine were added thereto with stirring. The reaction mixture was maintained at 40° C. for about 10 minutes. To this mixture was added dropwise 0.3 g of pyridine over 5 minutes. The whole mixture was vigorously and continuously stirred for 2 hours while maintaining the temperature of 40° to 45° C. to complete the reaction. The mixture was then treated according to the same procedure as Example 7 to obtain 35.3 g (Yield 92%) of the title compound.
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-de6c13b2380f48f383d6b53ff47c0c5a |
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| Source note | uspto-grants-1996_07 |
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