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HRID 1290469作成日:2026年10月26日

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

https://huagongshe.com/reaction/1290469

反応式

関与物質

役割名称HCID仕込み量
反応物1-(4-Pyridyl)piperazineHCID 70517—
反応物Benzeneacetic acid, 4-(chloroacetyl)-, methyl esterHCID 11128026—
溶媒AcetonitrileHCID 6342—
生成物Methyl 4-[2-[4-(4-pyridyl)piperazin-1-yl]acetyl]phenylacetateHCID 18918371—

反応手順

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%.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05750754
出典データセットuspto-grants-1998_05
ORD IDord-ce524f5859424e0baca5fa83425b029d
出典メモuspto-grants-1998_05