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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2387188Generated: October 26, 2026

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

https://huagongshe.com/reaction/2387188

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant1,4-Bis(diphenylphosphino)butaneHCID 82124—
Reactant1H-Indol-2-ylboronic acidHCID 22567358—
Reactant(3-Amino-6-bromo-pyrazin-2-yl)-pyridin-3-yl-methanoneHCID 86634541—
CatalystBis(benzonitrile)palladium chlorideHCID 498840—
SolventEthanolHCID 702—
SolventEthyl AcetateHCID 8857—
SolventSodium BicarbonateHCID 516892—
Product[3-Amino-6-(1h-indol-5-yl)-pyrazin-2-yl]-pyridin-3-yl-methanoneHCID 44233093—

Reaction Steps

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]+

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08268834B2
Source datasetuspto-grants-2012_09
ORD IDord-927d1354443e4164a44001ee57b48804
Source noteuspto-grants-2012_09