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HRID 864825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/864825

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.; 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%.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05563141
出典データセットuspto-grants-1996_10
ORD IDord-3487e30caa4241b7a9d44c16a7af5429
出典メモuspto-grants-1996_10