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HRID 79206作成日:2026年10月24日

Potassium Carbonate → Ethyl 2-(4-((6-chloropyridin-3-yl)methyl)piperazin-1-yl)acetate

https://huagongshe.com/ja/reaction/79206

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium CarbonateHCID 11430—
反応物2-Chloro-5-(chloromethyl)pyridineHCID 155479—
反応物Ethyl piperazine-1-acetateHCID 207112—
溶媒AcetonitrileHCID 6342—
生成物Ethyl 2-(4-((6-chloropyridin-3-yl)methyl)piperazin-1-yl)acetateHCID 5830020430.8%

反応手順

To a stirred suspension of 2-chloro-5-(chloromethyl)pyridine (2.0 g, 12 mmol) in acetonitrile (60 mL) was added potassium carbonate (1.5 mL, 25 mmol) followed by 1-(ethoxycarbonylmethyl)piperazine (2.0 mL, 12 mmol). The resulting mixture was stirred at room temperature for 19 h. The mixture was filtered through celite and the filter cake was washed with ethyl acetate. The filtrate was concentrated in vacuo and the residue was subjected to combi-flash column chromatography (methanol/DCM with Et3N) to give compound 348 (1.1 g, 30% yield) as a colorless liquid. 1H NMR (500 MHz, CHLOROFORM-d) δ ppm 8.31 (1 H, d, J=2.0 Hz), 7.66 (1 H, d, J=6.1 Hz), 7.28 (1 H, d, J=8.1 Hz), 4.18 (2 H, q, J=7.1 Hz), 3.50 (2 H, br. s.), 3.21 (2 H, s), 2.36-2.77 (8 H, m), 1.27 (3 H, t, J=7.2 Hz). LCMS-ESI (POS), M/Z, M+1: Found 298.1.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08841312B2
出典データセットuspto-grants-2014_09
ORD IDord-0dda912a2cf9474aba37226729539639
出典メモuspto-grants-2014_09