Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | HCID 86720245 | HCID 86720245 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 86720246 | HCID 86720246 | 57.1% |
Reaction Steps
To a solution of 2-(3-chloro-2-pyridyl)-N-[2,4-dichloro-6-hydroxycarbonyl-phenyl]-5-(trifluoromethyl)pyrazole-3-carboxamide (18.4 g, 38.3 mmol) in methylene chloride (130 mL) was added acetic anhydride (39.4 mL, 417 mmol). The reaction was then heated to 55° C. for 2 h and then stirred for a further 16 h at room temperature. The resulting solid was filtered and washed with cold methylene chloride. Trituration with diethyl ether afforded the title compound (10.1 g, 57%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09044016B2 |
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| Source dataset | uspto-grants-2015_06 |
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| ORD ID | ord-8d6ddd41ccfc452b9896e2f5d98b0224 |
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| Source note | uspto-grants-2015_06 |
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