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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 490174생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/490174

반응식

참여 물질

역할이름HCID투입량
반응물FormaldehydeHCID 712—
반응물Potassium CarbonateHCID 11430—
반응물m-(Trifluoromethyl)benzamideHCID 74535—
반응물1',2',3',6'-Tetrahydro-2,4'-bipyridine hydrochlorideHCID 68872830—
용매EthanolHCID 702—
생성물N-(3',6'-dihydro-2,4'-bipyridin-1'(2'H)-ylmethyl)-3-(trifluoromethyl)benzamideHCID 6887359141.5%

반응 단계

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-trifluoromethylbenzamide (95 mg, 0.5 mmol), 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 15 mg (41%) pure compound. 1H NMR (500 MHz, DMSO-d6) δ 2.58 (m, 2H), 2.80 (t, J=4 Hz, 2H), 3.28 (m, 2H), 4.32 (d, J=5 Hz, 2H), 6.71 (m, 1H), 7.22 (m, 1H), 7.52 (d, J=6 Hz, 1H), 7.72 (m, 2H), 7.95 (d, J=6 Hz, 1H), 8.22 (m, 2H), 8.52 (m, 1H), 9.08 (t, J=5 Hz, 1H); MS (ESI/APCI−) m/e 360 (M−H)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07528134B2
출처 데이터셋uspto-grants-2009_05
ORD IDord-48c14669a0f547d5a86023b09cdc2bfc
출처 메모uspto-grants-2009_05