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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1028975생성일: 2026년 10월 27일

Potassium Phosphate, Tribasic → 6-(2-([1,2,4]Triazolo[4,3-a]pyridin-3-yl)-6-methylphenyl)-3-morpholinoquinolin-2-amine

https://huagongshe.com/reaction/1028975

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참여 물질

역할이름HCID투입량
반응물Potassium Phosphate, TribasicHCID 62657—
반응물Dicyclohexyl(2',4',6'-tripropyl-[1,1'-biphenyl]-2-yl)phosphineHCID 21081571—
반응물3-(2-Bromo-3-methylphenyl)-[1,2,4]triazolo[4,3-a]pyridineHCID 67324963—
반응물3-Morpholino-6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)quinolin-2-amineHCID 67347995—
촉매Bis(dibenzylideneacetone)palladiumHCID 9811564—
생성물6-(2-([1,2,4]Triazolo[4,3-a]pyridin-3-yl)-6-methylphenyl)-3-morpholinoquinolin-2-amineHCID 53328996—

반응 조건

온도140 °C

반응 단계

A mixture of 3-(2-bromo-3-methylphenyl)-[1,2,4]triazolo[4,3-a]pyridine (0.32 g, 1.111 mmol), 3-morpholino-6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)quinolin-2-amine (0.17 g, 0.479 mmol, prepared as in Example 2, Step 1-2), 2-(dicyclohexylphosphino)-2′,4′,6′,-tri-1-propyl-1,1′-biphenyl (0.046 g, 0.096 mmol), potassium phosphate, anhydrous (0.198 mL, 2.393 mmol), and Pd2(dba)3 (0.044 g, 0.048 mmol) was purged with N2 followed by the addition of degassed dioxane (2 mL) and water (1.0 mL). The resulting mixture was heated in microwave at 140° C. for 12 min. The reaction was filtered, concentrated, and the resulting crude material was chromatographed on silica gel using gradient 2:1 hexanes/EtOAc and 0-5% 2M NH3 in MeOH/DCM to afford a light yellow solid. It was repurified by HPLC to afford 6-(2-([1,2,4]triazolo[4,3-a]pyridin-3-yl)-6-methylphenyl)-3-morpholinoquinolin-2-amine as a white solid. MS (ESI, pos. ion) m/z: 437 (M+1).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08735384B2
출처 데이터셋uspto-grants-2014_05
ORD IDord-e305a56c6df94473ad2eec06d29f82b6
출처 메모uspto-grants-2014_05