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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 336404생성일: 2026년 10월 25일

Cesium carbonate → 5-(4-Methoxypiperidin-1-yl)-[1,2,4]triazolo[1,5-a]pyridin-2-amine

https://huagongshe.com/reaction/336404

반응식

참여 물질

역할이름HCID투입량
반응물Cesium carbonateHCID 10796—
반응물4-MethoxypiperidineHCID 77666—
반응물5-Bromo-[1,2,4]triazolo[1,5-a]pyridin-2-amineHCID 25215939—
촉매Bis(dibenzylideneacetone)palladiumHCID 9811564—
촉매2-Dicyclohexylphosphino-2',4',6'-triisoprophylbiphenylHCID 11155794—
용매DimethylformamideHCID 6228—
생성물5-(4-Methoxypiperidin-1-yl)-[1,2,4]triazolo[1,5-a]pyridin-2-amineHCID 59186352693%

반응 조건

온도180 °C

반응 단계

A suspension of 5-bromo[1,2,4]triazolo[1,5-a]pyridin-2-amine (69.2 mg, 0.325 mmol, 1 equiv), 4-methoxypiperidine (150 mg, 1.3 mmol, 4.0 equiv), cesium carbonate (212 mg, 0.652 mmol, 2.00 equiv), XPhos (16.9 mg, 0.0354 mmol, 0.109 equiv), and tris(dibenzylideneacetone)dipalladium (0) (9.3 mg, 0.010 mmol, 0.031 equiv) in N,N-dimethylformamide (2 mL) was heated to 180° C. in the microwave for 15 min. The reaction mixture was concentrated in vacuo. The resulting residue was partitioned between ethyl acetate (5 mL) and saturated aqueous sodium chloride solution (5 mL). The aqueous was extracted with ethyl acetate (2×5 mL). The combine organic was dried over anhydrous sodium sulfate, filtered, and concentrated. Purification by flash column chromotagraphy (95:5 dichloromethane/methanol) afforded a white solid (557 mg, 67%). LCMS (ESI) m/z: 248.3. NMR (500 MHz, CDCl3), δ: 7.32 (m, 1H), 7.05 (m, 1H), 6.23 (m, 1H), 4.39 (br s, 2H), 3.66 (m, 2H), 3.48 (m, 1H), 3.41 (s, 3H), 3.18 (m, 2H), 2.08 (m, 2H), 1.89 (m, 2H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08889673B2
출처 데이터셋uspto-grants-2014_11
ORD IDord-f35e097a1ff5487da5b8e60e39d33109
출처 메모uspto-grants-2014_11