戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 2200作成日:2026年10月24日

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

https://huagongshe.com/ja/reaction/2200

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Methyl 4-bromoacetylphenoxyacetateHCID 243438—
溶媒AcetonitrileHCID 6342—
生成物Methyl 4-[2-[4-(4-pyridyl)piperazin-1-yl]acetyl]phenoxyacetateHCID 22118604—

反応手順

A solution of methyl 4-bromoacetylphenoxyacetate (4.3 g) in acetonitrile (50 ml) was added dropwise over 40 minutes to a stirred solution of 1-(4-pyridyl)piperazine (4.9 g) in acetonitrile (100 ml). Stirring was continued for a further 1.5 hours, then the solution was filtered and the filtrate evaporated in vacuo. The solid residue was triturated with water (50 ml), then dried and suspended in methylene chloride (50 ml). The suspension was then filtered and the filtrate concentrated to a small volume. Purification by flash chromatography on neutral alumina eluting first with dichloromethane, then 0.5% v/v methanol/dichloromethane and finally 1% v/v methanol/dichloromethane gave the title compound, 1.93 g, as a solid: m.p. 150°-152° C.; NMR(d6DMSO) δ 8.14(2H,d), 7.98(2H,d), 7.03(2H,d), 6.78(2H,d), 4.90(2H,s), 3.83(2H,s), 3.72(3H,s), 3.34(4H,bt), 2.65(4H,bt); m/e 370 (M+H)+ ; calculated for C20H23N3O4 : C, 65.0; H, 6.3; N, 11.4 found: C 65.2; H, 6.4; N,

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05728701
出典データセットuspto-grants-1998_03
ORD IDord-60883984e0a345f69557d95970310d78
出典メモuspto-grants-1998_03