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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1290513생성일: 2026년 10월 23일

1-(4-Pyridyl)piperazine → Ethyl 4-[2-[4-(4-pyridyl)piperazin-1-yl]acetyl]phenoxyacetate

https://huagongshe.com/ko/reaction/1290513

반응식

참여 물질

역할이름HCID투입량
반응물1-(4-Pyridyl)piperazineHCID 70517—
반응물Ethyl 2-[4-(2-bromoacetyl)phenoxy]acetateHCID 18408936—
용매AcetonitrileHCID 6342—
생성물Ethyl 4-[2-[4-(4-pyridyl)piperazin-1-yl]acetyl]phenoxyacetateHCID 18918266—

반응 단계

Ethyl 4-bromoacetylphenoxyacetate (6.0 g) was added to a stirred, cooled (4° C.) solution of 1-(4-pyridyl)piperazine (6.5 g) in acetonitrile (225 ml). Stirring was continued for 1 hour at 4° C., then overnight at ambient temperature when the precipitated solid was removed by filtration. The filtrate was evaporated in vacuo and the solid residue triturated with water, filtered, then washed with water and dried. Recrystallization from a small volume of ethanol gave the title compound, 1.71 g, as a cream coloured solid: m.p. 113°-114° C.; NMR (d6DMSO) δ8.15(2H,d), 7.98(2H,d), 7.02(2H,d), 6.80(2H,d), 4.89(2H,d), 4.17(2H,q), 3.84(2H,s), 3.32(4H,t), 2.62(4H,t) 1.22(3H,t); m/e 384 (M+H)+ ; calculated for C21H25N3O4 : C, 65.8; H, 6.6; N, 11.0. found: C, 65.5; H, 6.6; N, 10.8%.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05750754
출처 데이터셋uspto-grants-1998_05
ORD IDord-ca3c42b492ea439fa1bd5336aa38c091
출처 메모uspto-grants-1998_05