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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Formaldehyde | HCID 712 | — |
| 반응물 | Potassium Carbonate | HCID 11430 | — |
| 반응물 | m-(Trifluoromethyl)benzamide | HCID 74535 | — |
| 반응물 | 1',2',3',6'-Tetrahydro-2,4'-bipyridine hydrochloride | HCID 68872830 | — |
| 용매 | Ethanol | HCID 702 | — |
| 생성물 | N-(3',6'-dihydro-2,4'-bipyridin-1'(2'H)-ylmethyl)-3-(trifluoromethyl)benzamide | HCID 68873591 | 41.5% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 특허 번호 | US07528134B2 |
|---|
| 출처 데이터셋 | uspto-grants-2009_05 |
|---|
| ORD ID | ord-48c14669a0f547d5a86023b09cdc2bfc |
|---|
| 출처 메모 | uspto-grants-2009_05 |
|---|