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HRID 490176作成日:2026年10月26日

Formaldehyde → N-(3',6'-dihydro-2,4'-bipyridin-1'(2'H)-ylmethyl)cyclohexanecarboxamide

https://huagongshe.com/reaction/490176

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CyclohexanecarboxamideHCID 14283—
反応物1',2',3',6'-Tetrahydro-2,4'-bipyridine hydrochlorideHCID 68872830—
溶媒EthanolHCID 702—
生成物N-(3',6'-dihydro-2,4'-bipyridin-1'(2'H)-ylmethyl)cyclohexanecarboxamideHCID 6887238464%

反応手順

A mixture of 1′,2′,3′,6′-tetrahydro-[2,4′]bipyridinyl hydrochloride (20 mg, 0.10 mmol, Saari, W. S.; et al. J. Med. Chem. 1984, 27, 1182), paraformaldehyde (30 mg, 1 mmol), cyclohexanecarboxylic acid amide (64 mg, 0.5 mmol, Aldrich), and 42 mg of potassium carbonate (0.3 mmol) in 2.5 mL absolute ethyl alcohol was heated to reflux under nitrogen overnight. The mixture was cooled to room temperature, filtered, and the solvent was removed. The residue was purified by flash column chromatography on silica gel (10% methanol:ethyl acetate) to give 19 mg (64%) pure compound. 1H NMR (500 MHz, DMSO-d6) δ 1.19 (m, 4H), 1.26 (m, 2H), 1.61 (m, 1H), 1.68 (m, 3H), 2.18 (m, 1H), 2.55 (m, 2H), 2.68 (m, 2H), 3.18 (m, 2H), 4.02 (d, J=5 Hz, 2H), 6.68 (m, 1H), 7.22 (m, 1H), 7.52 (d, J=6 Hz, 1H), 7.73 (t, J=6 Hz, 1H), 8.02 (t, J=5 Hz, 1H), 8.52 (m, 1H); MS (ESI/APCI−) m/e 298 (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-3c91708860f2402382132a49cb1bde89
出典メモuspto-grants-2009_05