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HRID 490185作成日:2026年10月26日

Formaldehyde → 3,5-dimethoxy-N-{[4-(2-pyridinyl)-1-piperazinyl]methyl}benzamide

https://huagongshe.com/reaction/490185

反応式

関与物質

役割名称HCID仕込み量
反応物FormaldehydeHCID 712—
反応物Potassium CarbonateHCID 11430—
反応物3,5-DimethoxybenzamideHCID 72878—
反応物1-(2-Pyridyl)piperazineHCID 94459—
溶媒EthanolHCID 702—
生成物3,5-dimethoxy-N-{[4-(2-pyridinyl)-1-piperazinyl]methyl}benzamideHCID 10428353108%

反応手順

A mixture of 1-pyridin-2-ylpiperazine (16 mg, 0.1 mmol, Aldrich), paraformaldehyde (30 mg, 1 mmol), 3,5-dimethoxybenzamide (91 mg, 0.5 mmol, Lancaster), and 42 mg of potassium carbonate (0.3 mmol) in 2 mL absolute ethyl alcohol was heated to reflux under nitrogen overnight. The mixture was cooled to room temperature, filtered, and the solvent was removed under reduced pressure. The residue was purified by flash column chromatography on silica gel (10% methanol:ethyl acetate) to give 38.5 mg (72%) pure compound. 1H NMR (500 MHz, DMSO-d6) δ 2.59 (t, J=4 Hz, 4H), 3.48 (t, J=4 Hz, 4H), 3.78 (s, 6H), 4.20 (d, J=5 Hz, 1H), 6.62 (m, 2H), 6.81 (d, J=6 Hz, 1H), 7.03 (s, 2H), 7.50 (t, J=6 Hz, 1H), 8.10 (d, J=5 Hz, 1H), 8.78 (t, J=5 Hz, 1H); MS (ESI/APCI−) m/e 355 (M−H)+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07528134B2
出典データセットuspto-grants-2009_05
ORD IDord-5c50397a3a4c428c9855a1345a025889
出典メモuspto-grants-2009_05