Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2229152생성일: 2026년 10월 25일
Potassium Carbonate → 2,5-Pyrrolidinedione, 1-[3-[4-(2-methoxyphenyl)-1-piperazinyl]propyl]-
https://huagongshe.com/reaction/2229152
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Potassium Carbonate | HCID 11430 | — |
| 반응물 | Succinimide | HCID 11439 | — |
| 반응물 | 1-(3-Chloropropyl)-4-(2-methoxyphenyl)piperazine | HCID 622669 | — |
| 촉매 | Tetrabutylammonium Bromide | HCID 74236 | — |
| 용매 | Acetone | HCID 180 | — |
| 생성물 | 2,5-Pyrrolidinedione, 1-[3-[4-(2-methoxyphenyl)-1-piperazinyl]propyl]- | HCID 9949436 | — |
반응 단계
Scheme-I: A mixture of 2,5-dioxopyrrolidine (3.68 g, 37.24 mmol), 1-[4-(2-methoxyphenyl)-piperazin-1-yl]-3-chloropropane (10.0 g, 37.24 mmol), potassium carbonate (7.70 g, 55.8 mmol) and tetrabutylammonium bromide (2.38 g, 7.4 mmol) in acetone (100 ml) was refluxed for 12 hours at 80° C. with stirring. The solvent was evaporated off in vacuo and the residue was taken up in water (80 ml). The aqueous solution was extracted with chloroform (3×50 ml) and the organic layers combined, washed with water (2×50 ml), dried over Na2SO4 and evaporated in vacuo to give the title compound. The product was purified by column chromatography over flash silica gel using chloroform-methanol (99:1) as eluent; yield 8.00 g (65%) in oil. The hydrochloride salt was prepared by the method described above mp 199-202° C.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 특허 번호 | US06420366B1 |
|---|
| 출처 데이터셋 | uspto-grants-2002_07 |
|---|
| ORD ID | ord-253e493a708f441e9abab59575e7ea3d |
|---|
| 출처 메모 | uspto-grants-2002_07 |
|---|