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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2092541생성일: 2026년 10월 26일

Dimethylformamide → 5-[7-(3-Methanesulfonyl-phenyl)-4-morpholin-4-yl-quinazolin-2-yl]-pyridin-2-ylamine

https://huagongshe.com/reaction/2092541

반응식

참여 물질

역할이름HCID투입량
반응물DimethylformamideHCID 6228—
반응물Cesium carbonateHCID 10796—
반응물5-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin-2-amineHCID 2756555—
반응물4-(2-Chloro-7-(3-(methylsulfonyl)phenyl)quinazolin-4-yl)morpholineHCID 86665760—
촉매HCID 178418476HCID 178418476—
용매WaterHCID 962—
생성물5-[7-(3-Methanesulfonyl-phenyl)-4-morpholin-4-yl-quinazolin-2-yl]-pyridin-2-ylamineHCID 6751442874%

반응 조건

온도95 °C

반응 단계

To a 50 mL round bottom flask, 2-chloro-7-(3-methanesulfonyl-phenyl)-4-morpholin-4-yl-quinazoline (0.15 g, 0.00037 mol), 2-aminopyridine-5-boronic acid pinacol ester (0.122 g, 0.0005568 mol), cesium carbonate (0.243 g, 0.00074 mol), DMF (4 mL) and water (2 mL) were added. The reaction mixture was degassed with nitrogen for 5-10 min. To the same reaction flask, Pd(PPh3)2Cl2 (0.013 g, 0.000018 mol) was added and again degassed with nitrogen for 5-10 min. The reaction mixture was stirred at 95° C. for 2 h. The reaction mixture was cooled and diluted with ethyl acetate. The organic layer was washed with water, brine and dried over sodium sulfate. The solvent was removed under reduced pressure to afford the crude product. The crude product was purified using column chromatography (60-120 silica gel, 5% MeOH in chloroform) to yield the title compound (125 mg, 74%). LC-MS (ESI): Calculated mass: 461.2; Observed mass: 462.1 [M+H]+ (RT: 0.17 min).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08440662B2
출처 데이터셋uspto-grants-2013_05
ORD IDord-d1be9849c5e84fdf8b2b739665d8df77
출처 메모uspto-grants-2013_05