関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Formaldehyde | HCID 712 | — |
| 反応物 | Potassium Carbonate | HCID 11430 | — |
| 反応物 | 3,5-Dimethoxybenzamide | HCID 72878 | — |
| 反応物 | 1',2',3',6'-Tetrahydro-2,4'-bipyridine hydrochloride | HCID 68872830 | — |
| 溶媒 | Ethanol | HCID 702 | — |
| 生成物 | N-(3',6'-dihydro-2,4'-bipyridin-1'(2'H)-ylmethyl)-3,5-dimethoxybenzamide | HCID 68875562 | 55% |
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), 3,5-dimethoxybenzamide (91 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 (55%) pure compound. 1H NMR (500 MHz, DMSO-d6) δ 2.59 (m, 2H), 2.79 (t, J=4 Hz, 2H), 3.30 (m, 2H), 3.79 (s, 3H), 3.80 (s, 3H), 4.25 (d, J=5 Hz, 2H), 6.65 (s, 1H), 6.71 (m, 1H), 7.02 (s, 2H), 7.22 (m, 1H), 7.52 (d, J=6 Hz, 1H), 7.75 (t, J=6 Hz), 8.52 (m, 1H), 8.88 (t, J=5 Hz, 1H); MS (ESI/APCI−) m/e 352 (M−H)+.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07528134B2 |
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| 出典データセット | uspto-grants-2009_05 |
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| ORD ID | ord-31b710855b084b50abdaa1a302ee154e |
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| 出典メモ | uspto-grants-2009_05 |
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