HuagongsheHuagongshe Chemistry Print Report · For research reference only
Piperazine → 2-(4-Bromophenyl)-2-isopropyl-5-(4-phenylpiperazine-1-yl)pentanoic acid methyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Piperazine | HCID 4837 | — |
| Reactant | 1-Phenylpiperazine | HCID 7096 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Sodium Iodate | HCID 23675764 | — |
| Reactant | 5-Bromo-2-(4-bromophenyl)-2-isopropylpentanoic acid methyl ester | HCID 46855860 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 2-(4-Bromophenyl)-2-isopropyl-5-(4-phenylpiperazine-1-yl)pentanoic acid methyl ester | HCID 46186740 | — |
Reaction Steps
After the 5-bromo-2-(4-bromophenyl)-2-isopropylpentanoic acid methyl ester (200 mg, 1 eq) was dissolved in acetonitrile, 4-phenylpiperazine (70 mg, 1 eq) as a piperazine derivative, Et3N (0.06 ml, 1.2 eq), and sodium iodate were added into the solution and heated and refluxed for 3 hours. When the reaction was completed, the precipitate was filtrated and the mixture was vacuum distilled and extracted with ethyl acetate and water. After the organic layer was washed with 1N HCl and saturated NaHCO3, the target compound 2-(4-bromophenyl)-2-isopropyl-5-(4-phenylpiperazine-1-yl)pentanoic acid methyl ester was obtained by drying the mixture with anhydrous sodium sulfate and removing the solvent at low pressures (69 mg, 42%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07939672B2 |
| Source dataset | uspto-grants-2011_05 |
| ORD ID | ord-5be30e553d664163ac3b72e36c175460 |
| Source note | uspto-grants-2011_05 |