Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Trifluoroacetic anhydride | HCID 9845 | — |
| Reactant | 1,4-Dioxane | HCID 31275 | — |
| Reactant | HCID 54565766 | HCID 54565766 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 54402406 | HCID 54402406 | — |
Reaction Steps
A mixture of 0.79 g (2.91 mmol) 1-(5-difluoromethoxy-1-methyl-3-pyrazolyl)-5-methyl-4-pyrazolecarboxamide, 0.46 g (5.85 mmol) pyridine and 20 ml 1,4-dioxane was cooled to 5° C. and 0.74 g (3.51 mmol) trifluoroacetic anhydride was added dropwise. The mixture was stirred for 3 hours at room temperature. It was then added to 100 ml water and extracted 4 times with ethyl acetate. The organic phase was dried over magnesium sulfate and concentrated.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05756424 |
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| Source dataset | uspto-grants-1998_05 |
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| ORD ID | ord-88df9e789e814f26b16a17a530a55bc1 |
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| Source note | uspto-grants-1998_05 |
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