Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Phenylacetylene | HCID 10821 | — |
| Reactant | HCID 15340994 | HCID 15340994 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Pyrrolidine | HCID 31268 | — |
| Product | HCID 18677777 | HCID 18677777 | 86% |
Reaction Steps
To a stirred solution of 1-[4-(methylsulfonyl)phenyl]-5-(4-bromophenyl)-3-trifluoromethyl-1H-pyrazole (445 mg; 1 mmol) and phenylacetylene (102 mg; 1 mmol) in pyrrolidine (2 mL) was added tetrakis(triphenylphosphine)palladium (35 mg) under a nitrogen atmosphere, and the mixture was heated at 80° C. for 1 hour. After cooling, the volatiles were removed by evaporation. The residue was purified by flash chromatography (SiO2) eluting with ethyl acetate/hexane (1:3) to give the title compound (0.4 g, 86% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06506779B1 |
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| Source dataset | uspto-grants-2003_01 |
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| ORD ID | ord-3ee9a0065c434af499016a88b973911d |
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| Source note | uspto-grants-2003_01 |
|---|