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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2204생성일: 2026년 10월 23일

1-(4-Pyridyl)piperazine → Methyl 4-[2-[4-(4-pyridyl)piperazin-1-yl]acetyl]phenylacetate

https://huagongshe.com/ko/reaction/2204

반응식

참여 물질

역할이름HCID투입량
반응물1-(4-Pyridyl)piperazineHCID 70517—
반응물Benzeneacetic acid, 4-(chloroacetyl)-, methyl esterHCID 11128026—
용매AcetonitrileHCID 6342—
생성물Methyl 4-[2-[4-(4-pyridyl)piperazin-1-yl]acetyl]phenylacetateHCID 18918371—

반응 단계

A solution of methyl 4-chloroacetylphenylacetate (260 mg) in acetonitrile (4 ml) was added dropwise over 15 minutes to a stirred solution of 1-(4-pyridyl)piperazine (375 mg) in acetonitrile (10 ml) and the mixture stirred overnight. The supernatent was decanted from the solid formed, concentrated in vacuo and purified by flash chromatography on neutral alumina, eluting with dichloromethane then 0.25% v/v methanol/dichloromethane and finally 0.5% v/v methanol dichloromethane. Concentration of the fractions in vacuo gave the title compound, 96 mg, as a white crystalline solid: m.p. 127°-129° C.; NMR (d6 DMSO) δ 8.15(2H,d), 7.98(2H,d), 7.41(2H,d), 6.81(2H,d), 3.91(2H,s), 3.78(2H,s), 3.53(3H,s), 3.33(4H,t), 2.64(4H,t); m/e 354(M+H )+ ; calculated for C20H23N3O3 : C, 68.0; H, 6.6; N, 11.9. found: C, 68.2; H, 6.6; N, 11.9%.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05728701
출처 데이터셋uspto-grants-1998_03
ORD IDord-dec26e4a500a423b998283ba15ea943b
출처 메모uspto-grants-1998_03