돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2287339생성일: 2026년 10월 25일

Potassium Carbonate → 2,5-Pyrrolidinedione, 1-[3-[4-(2-methoxyphenyl)-1-piperazinyl]propyl]-

https://huagongshe.com/reaction/2287339

반응식

참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물SuccinimideHCID 11439—
반응물1-(3-Chloropropyl)-4-(2-methoxyphenyl)piperazineHCID 622669—
촉매Tetrabutylammonium BromideHCID 74236—
용매AcetoneHCID 180—
생성물2,5-Pyrrolidinedione, 1-[3-[4-(2-methoxyphenyl)-1-piperazinyl]propyl]-HCID 9949436—

반응 조건

온도80 °C

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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06083950
출처 데이터셋uspto-grants-2000_07
ORD IDord-dc6626ca82d84731a462145f123738e8
출처 메모uspto-grants-2000_07