Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 5183025 | HCID 5183025 | — |
| Reactant | HCID 22367730 | HCID 22367730 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 70087477 | HCID 70087477 | — |
Reaction Steps
A mixture of 300 mg of 1-[bis(4-fluorophenyl) methyl]homopiperazine and 300 mg of N-(1-adamantyl) -2-bromopropionamide Was dissolved in 20 ml of a 1:1 by volume mixture of tetrahydrofuran and N,N-dimethylformamide, and then 100 mg of anhydrous potassium carbonate were added to the resulting solution. The reaction mixture was stirred at 90° C. for hours, and then ethyl acetate was added, and the organic layer was separated. The organic layer was washed three times with water, and then dried over anhydrous magnesium sulfate. The solvent was removed by evaporation under reduced pressure, and the residue was subjected to silica gel thin layer chromatography using a 1:1 by volume mixture of cyclo hexane and ethyl acetate as the developing solvent, to give a purified 1-[bis(4-fluorophenyl)methyl]-4-[1-(1-adamantylcarbamoyl)ethyl]homopiperazine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05028610 |
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| Source dataset | uspto-grants-1991_07 |
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| ORD ID | ord-6cc850405e3d48db811e233c390c9c42 |
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| Source note | uspto-grants-1991_07 |
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