Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | tert-Butyl methyl ether | HCID 15413 | — |
| Reactant | HCID 2782707 | HCID 2782707 | — |
| Reactant | 3-(Difluoromethyl)-1-methyl-1 H-pyrazole-4-carbonyl chloride | HCID 15340110 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 11955084 | HCID 11955084 | — |
Reaction Steps
At room temperature, 0.29 g of 3-difluoromethyl-1-methyl-1H-pyrazole-4-carbonyl chloride was added dropwise to a solution of 0.36 g of 4′-trifluoromethyl-2-aminobiphenyl and 0.18 g of pyridine in 10 ml of toluene, after which the mixture was stirred at room temperature for 16 hours. 30 ml of methyl tert-butyl ether were added, and the organic phase was washed successively with 2% strength hydrochloric acid, 2% strength aqueous sodium hydroxide solution and then with dilute sodium chloride solution. The organic phase was dried and concentrated under reduced pressure. The crude product was stirred with 5 ml of diisopropyl ether. The solid that remained was separated off and dried. This gave 0.45 g of the desired product as a white powder; m.p. 164-165° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07799334B2 |
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| Source dataset | uspto-grants-2010_09 |
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| ORD ID | ord-647a0745bed04e9d9149580db0bff8f0 |
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| Source note | uspto-grants-2010_09 |
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