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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2387188생성일: 2026년 10월 27일

Sodium Carbonate → [3-Amino-6-(1h-indol-5-yl)-pyrazin-2-yl]-pyridin-3-yl-methanone

https://huagongshe.com/reaction/2387188

반응식

참여 물질

역할이름HCID투입량
반응물Sodium CarbonateHCID 10340—
반응물1,4-Bis(diphenylphosphino)butaneHCID 82124—
반응물1H-Indol-2-ylboronic acidHCID 22567358—
반응물(3-Amino-6-bromo-pyrazin-2-yl)-pyridin-3-yl-methanoneHCID 86634541—
촉매Bis(benzonitrile)palladium chlorideHCID 498840—
용매EthanolHCID 702—
용매Ethyl AcetateHCID 8857—
용매Sodium BicarbonateHCID 516892—
생성물[3-Amino-6-(1h-indol-5-yl)-pyrazin-2-yl]-pyridin-3-yl-methanoneHCID 44233093—

반응 단계

Bis(benzonitrile)palladium(II)chloride (5.2 mg, 0.013 mmol) and 1,4-bis(diphenylphosphino)butane (6.7 mg, 0.015 mmol) in toleune (0.6 ml) are stirred for 20 minutes. (3-Amino-6-bromo-pyrazin-2-yl)-pyridin-3-yl-methanone (Intermediate AA) (0.075 g, 0.27 mmol), 5-indoylboronic acid (0.056 g, 0.35 mmol), ethanol (0.36 ml) and 1M Na2CO3 (0.65 ml) are added and the reaction is heated using microwave radiation at 140° C. for 20 minutes. The mixture is diluted with EtOAc and sat. aq. NaHCO3. The layers are separated and the aqueous layer is extracted with EtOAc. The combined organic extracts are dried (MgSO4), and purified by preperative HPLC (0-100% MeCN in water −0.1% TFA) to yield the title compound as an orange solid. 1H NMR (400 MHz, DMSO-d6) δ 11.27 (1H, s), 9.21 (1H, s), 9.09 (1H, s), 8.86 (1H, dd), 8.39-8.41 (1H, dt), 8.19 (1H, s), 7.99 (2H, s), 7.65-7.73 (2H, m), 7.5 (1H, d), 7.44 (1H, t), 6.53 (1H, s). MS m/z 316 [M+H]+

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08268834B2
출처 데이터셋uspto-grants-2012_09
ORD IDord-927d1354443e4164a44001ee57b48804
출처 메모uspto-grants-2012_09