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Piperazine → 2-(4-Bromophenyl)-2-isopropyl-5-(4-phenylpiperazine-1-yl)pentanoic acid methyl ester
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Piperazine | HCID 4837 | — |
| 反応物 | 1-Phenylpiperazine | HCID 7096 | — |
| 反応物 | Triethylamine | HCID 8471 | — |
| 反応物 | Sodium Iodate | HCID 23675764 | — |
| 反応物 | 5-Bromo-2-(4-bromophenyl)-2-isopropylpentanoic acid methyl ester | HCID 46855860 | — |
| 溶媒 | Acetonitrile | HCID 6342 | — |
| 生成物 | 2-(4-Bromophenyl)-2-isopropyl-5-(4-phenylpiperazine-1-yl)pentanoic acid methyl ester | HCID 46186740 | — |
反応手順
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%).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07939672B2 |
| 出典データセット | uspto-grants-2011_05 |
| ORD ID | ord-5be30e553d664163ac3b72e36c175460 |
| 出典メモ | uspto-grants-2011_05 |