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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2201088생성일: 2026년 10월 23일

Cesium carbonate → (R)-2-(5-cyano-3-fluoro-6-(quinolin-6-ylamino)pyridin-2-ylamino)butanamide

https://huagongshe.com/ko/reaction/2201088

반응식

참여 물질

역할이름HCID투입량
반응물Cesium carbonateHCID 10796—
반응물6-AminoquinolineHCID 11373—
반응물Binap, (A+-)-HCID 634876—
반응물(R)-2-(6-chloro-5-cyano-3-fluoropyridin-2-ylamino)butanamideHCID 86666160—
촉매palladium(II) acetateHCID 167845—
용매1,4-DioxaneHCID 31275—
생성물(R)-2-(5-cyano-3-fluoro-6-(quinolin-6-ylamino)pyridin-2-ylamino)butanamideHCID 67508846—

반응 조건

온도100 °C

반응 단계

The mixture of (R)-2-(6-chloro-5-cyano-3-fluoropyridin-2-ylamino)butanamide (235 mg, 0.92 mmol), 6-aminoquinoline (288 mg, 2.0 mmol), Pd(OAc)2 (44 mg, 0.22 mmol), racemic BINAP (136 mg, 0.22 mmol) and fine-powder cesium carbonate (1.0 g, 3.1 mmol) in 30 mL dioxane was degassed using argon stream for 3 min. It was then stirred at 100° C. in argon atmosphere for overnight. The mixture was cooled to RT, concentrated in vacuo, taken into 200 mL EtOAc and 50 mL water. The organic phase was separated and washed with brine. It was dried, concentrated and purified using silica flash column (35% EtOAc in DCM) to give (R)-2-(5-cyano-3-fluoro-6-(quinolin-6-ylamino)pyridin-2-ylamino)butanamide. It was dissolved in 4 mL DMSO. To it were added 2 mL 50% H2O2 and then powder potassium carbonate (91 mg, 0.66 mmol). The mixture was stirred at RT for 30 min. It was diluted with 4 mL 1N HCl. The mixture was subjected to reverse prep HPLC to isolate the title compound as HCl salt (210 mg). UV: 268, 297, 330 nm. M+H found for C19H19FN6O2: 383.4. NMR (CD3OD): 9.12 (1H, d, J=8.8 Hz), 8.90 (1H, s), 8.82 (1H, d, J=5.2 Hz), 8.03 (1H, d, J=8.8 Hz), 7.92 (1H, d, J=10.0 Hz), 7.85-7.82 (2H, m), 4.39 (1H, m), 2.09 (2H, m), 1.16 (3H, t, J=7.6 Hz) ppm.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09359375B2
출처 데이터셋uspto-grants-2016_06
ORD IDord-876bdac73ccb402cb734ff74767becb0
출처 메모uspto-grants-2016_06