Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2394-89-0 | HCID 12201199 | — |
| Reactant | HCID 19372890 | HCID 19372890 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 19372964 | HCID 19372964 | — |
Reaction Steps
A mixture of 2-acetylaminomethyl-5-(4-chlorobutyryl)thiophene (3 g), 1-(3-trifluoromethylphenyl)piperazine hydrobromide (4 g), potassium carbonate (3.5 g), potassium iodide (2 g), dimethylformamide (25 ml), and toluene (25 ml) was stirred at 60° C. for 7 hours. The reaction mixture was poured into water, extracted with toluene, and dried over magnesium sulfate, and then the solvent was distilled off under reduced pressure. The residue was purified by silica gel column chromatography, and converted to fumarate, followed by recrystallization from acetone to give 0.9 g of 1-(4-(5-acetylaminomethyl -2-thienyl)-4-oxobutyl)-4-(3-trifluoromethylphenyl)piperazine fumarate as white crystals, m.p. 135°-137° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05466691 |
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| Source dataset | uspto-grants-1995_11 |
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| ORD ID | ord-a24f0d1bc66a42e6aef6dd7024c4ac94 |
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| Source note | uspto-grants-1995_11 |
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