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HRID 266740作成日:2026年10月27日

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

https://huagongshe.com/reaction/266740

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Ethyl 2-[4-(2-bromoacetyl)phenoxy]acetateHCID 18408936—
溶媒AcetonitrileHCID 6342—
生成物Ethyl 4-[2-[4-(4-pyridyl)piperazin-1-yl]acetyl]phenoxyacetateHCID 18918266—

反応手順

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. Recrystallisation from a small volume of ethanol gave the title compound, 1.71 g, as a cream coloured solid: m.p. 113°-114° C.; (d6DMSO) δ 8.15 (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%.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05652242
出典データセットuspto-grants-1997_07
ORD IDord-2be04a7ca45447cfba0de30476c8ee08
出典メモuspto-grants-1997_07