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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2219생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/2219

반응식

참여 물질

역할이름HCID투입량
반응물1-(4-Pyridyl)piperazineHCID 70517—
반응물HCID 20315599HCID 20315599—
용매AcetonitrileHCID 6342—
생성물iso-Propyl 4-[2-[4-(4-pyridyl)piperazin-1-yl]acetyl]phenoxyacetateHCID 54144385—

반응 단계

iso-Propyl 4-bromoacetylphenoxyacetate (6.3 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. The filtrate was evaporated in vacuo and the residue partitioned between ethyl acetate and water. The organic phase was dried (MgSO4) and evaporated. Purification by flash chromatography on silica, eluting firstly with 0 to 10% v/v methanol/dichloromethane and then toluene/ethyl acetate/.880 ammonium hydroxide/ethanol (60:20:10:35 v/v/v/v), gave a cream solid. Recrystallisation from iso-propanol gave the title compound, 2.1 g: m.p. 121°-122° C.; NMR (d6DMSO) δ 8.14 (2H, d), 7.98 (2H, d), 7.02 (2H, d), 6.80 (2H, d), 4.99 (1H, m), 4.85 (2H, s), 3.84 (2H, s), 3.33 (4H, t), 2.62 (4H, t), 1.22 (6H, d); m/e 398 (M+H)+ ; calculated for C22H27N3O4 : C, 66.5; H, 6.9; N, 10.6. found: C, 65.8; H, 6.8; N, 10.4%.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05728701
출처 데이터셋uspto-grants-1998_03
ORD IDord-c0b95ca8088a4d46af3551fafa170fb2
출처 메모uspto-grants-1998_03