HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 490171Erstellt: 25. Oktober 2026
Formaldehyde → N-(3',6'-dihydro-2,4'-bipyridin-1'(2'H)-ylmethyl)-3-methoxybenzamide
https://huagongshe.com/reaction/490171
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Formaldehyde | HCID 712 | — |
| Edukt | Potassium Carbonate | HCID 11430 | — |
| Edukt | 3-Methoxybenzamide | HCID 98487 | — |
| Edukt | 1',2',3',6'-Tetrahydro-2,4'-bipyridine hydrochloride | HCID 68872830 | — |
| Lösungsmittel | Ethanol | HCID 702 | — |
| Produkt | N-(3',6'-dihydro-2,4'-bipyridin-1'(2'H)-ylmethyl)-3-methoxybenzamide | HCID 68874678 | 49% |
Reaktionsschritte
3-Methoxybenzamide (1.13 g, 7.5 mmol), K2CO3 (345 mg, 2.5 mmol), paraformaldehyde (0.5 g, 16 mmol), and 1′,2′,3′,6′-tetrahydro-2,4′-bipyridine hydrochloride (393 mg, 2 mmol) were combined in ethanol (25 ml) and refluxed for 18 hours. The reaction mixture was allowed to cool to room temperature and concentrated under reduced pressure. The residue was partitioned between ethyl acetate (80 mL) and water (80 mL). The organic layer was washed with brine (2×50 mL), dried over MgSO4, filtered, and the filtrate concentrated under reduced pressure. The residue was purified by flash chromatography on silica gel (elution with ethyl acetate:ethanol, 9.0:1.0) to provide the title compound (180 mg, 49% yield). 1H NMR (300 MHz, DMSO-d6) δ 2.58 (m, 2H), 2.76 (t, 2H, J=6 Hz), 3.29 (m, 2H), 3.80 (s, 3H), 4.27 (d, 2H, J=6 Hz), 6.70 (m, 1H), 7.09 (m, 1H), 7.22 (m, 1H), 7.42 (m, 4H), 7.72 (m, 1H), 8.51 (m, 1H), 8.83 (t, 1H, J=6 Hz); MS (DCI/NH3) m/e 324 (M+H)+.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07528134B2 |
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| Quelldatensatz | uspto-grants-2009_05 |
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| ORD ID | ord-430c647e9998449c99bced5335b09bf6 |
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| Quellennotiz | uspto-grants-2009_05 |
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