Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Piperazine → 2-(4-Bromophenyl)-2-isopropyl-5-(4-phenylpiperazine-1-yl)pentanoic acid methyl ester
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Piperazine | HCID 4837 | — |
| 반응물 | 1-Phenylpiperazine | HCID 7096 | — |
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | Sodium Iodate | HCID 23675764 | — |
| 반응물 | 5-Bromo-2-(4-bromophenyl)-2-isopropylpentanoic acid methyl ester | HCID 46855860 | — |
| 용매 | Acetonitrile | HCID 6342 | — |
| 생성물 | 2-(4-Bromophenyl)-2-isopropyl-5-(4-phenylpiperazine-1-yl)pentanoic acid methyl ester | HCID 46186740 | — |
반응 단계
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%).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US07939672B2 |
| 출처 데이터셋 | uspto-grants-2011_05 |
| ORD ID | ord-5be30e553d664163ac3b72e36c175460 |
| 출처 메모 | uspto-grants-2011_05 |