Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triphenylarsine | HCID 11773 | — |
| Reactant | Stannane, tributyl(1-methylethenyl)- | HCID 10871254 | — |
| Reactant | (2-Iodo-5-methanesulfonyl-phenyl)-[4-(4-trifluoromethyl-phenyl)-piperazin-1-yl]-methanone | HCID 59793691 | — |
| Catalyst | Copper iodide | HCID 83717 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 59853753 | HCID 59853753 | — |
Reaction Steps
A mixture of (2-Iodo-5-methanesulfonyl-phenyl)-[4-(4-trifluoromethyl-phenyl)-piperazin-1-yl]-methanone (Example 9; 100 mg, 0.186 mmol), Tributyl-isopropenyl-stannane (CAS: 100073-15-2; 74 mg, 0.223 mmol), Tris(dibenzylideneacetone)dipalladium chloroform complex (15.4 mg, 0.0149 mmol), Triphenylarsine (27 mg, 0.0856 mmol), Copper iodide (3.2 mg, 0.0167 mmol) in N,N-Dimethylformamide (1 ml) was heated at 90° C. for 75 minutes. The mixture was cooled to room temperature and DMF was evaporated under high vacuum. The residue was dissolved in Ethyl acetate and 4mL of a 30% Potassium fluoride solution were added. The mixture was stirred for 30 minutes. Then the aqueous phase was separated and extracted 2 times with Ethyl acetate. The organic phases were combined, washed with water, dried with Na2SO4 ,filtered and evaporated to dryness. The so obtained residue was chromatographed over SiO2 (Heptane/EtOAc 0% to 30% over 15 minutes) to provide the title compound (59 mg, 70% as a yellow solid).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07462617B2 |
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| Source dataset | uspto-grants-2008_12 |
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| ORD ID | ord-f4a430414fc64c5c8bc40073b7b3f930 |
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| Source note | uspto-grants-2008_12 |
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