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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2387188Erstellt: 26. Oktober 2026

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

https://huagongshe.com/reaction/2387188

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium CarbonateHCID 10340—
Edukt1,4-Bis(diphenylphosphino)butaneHCID 82124—
Edukt1H-Indol-2-ylboronic acidHCID 22567358—
Edukt(3-Amino-6-bromo-pyrazin-2-yl)-pyridin-3-yl-methanoneHCID 86634541—
KatalysatorBis(benzonitrile)palladium chlorideHCID 498840—
LösungsmittelEthanolHCID 702—
LösungsmittelEthyl AcetateHCID 8857—
LösungsmittelSodium BicarbonateHCID 516892—
Produkt[3-Amino-6-(1h-indol-5-yl)-pyrazin-2-yl]-pyridin-3-yl-methanoneHCID 44233093—

Reaktionsschritte

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]+

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08268834B2
Quelldatensatzuspto-grants-2012_09
ORD IDord-927d1354443e4164a44001ee57b48804
Quellennotizuspto-grants-2012_09