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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 490171생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/490171

반응식

참여 물질

역할이름HCID투입량
반응물FormaldehydeHCID 712—
반응물Potassium CarbonateHCID 11430—
반응물3-MethoxybenzamideHCID 98487—
반응물1',2',3',6'-Tetrahydro-2,4'-bipyridine hydrochlorideHCID 68872830—
용매EthanolHCID 702—
생성물N-(3',6'-dihydro-2,4'-bipyridin-1'(2'H)-ylmethyl)-3-methoxybenzamideHCID 6887467849%

반응 단계

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)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07528134B2
출처 데이터셋uspto-grants-2009_05
ORD IDord-430c647e9998449c99bced5335b09bf6
출처 메모uspto-grants-2009_05