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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1677397Generated: October 30, 2026

Potassium Carbonate → HCID 44208751, compound

https://huagongshe.com/reaction/1677397

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant3,4,5-Trimethoxybenzeneboronic acidHCID 2734390—
ReactantHCID 57830985HCID 57830985—
ReactantHCID 86646685HCID 86646685—
CatalystHCID 178418807HCID 178418807—
ProductHCID 44208751HCID 44208751—

Reaction Conditions

Temperature150 °C

Reaction Steps

A mixture of 1-(2-bromo-5H-pyrrolo[2,3-b]pyrazin-7-yl)-3-methyl-butan-1-one and 1-(2-chloro-5H-pyrrolo[2,3-b]pyrazin-7-yl)-3-methyl-butan-1-one (55 mg), potassium carbonate (95 mg, 0.69 mmol), 3,4,5-trimethoxyphenylboronic acid (47 mg, 0.22 mmol) and Pd(dppf)Cl2-DCM (16 mg, 0.02 mmol) was placed in a 5 ml microwave vial. The vial was capped and purged with nitrogen. Solvent was added (2 ml of 20% aqueous dioxane) and the vial was purged again with nitrogen. The reaction mixture was heated in a microwave reactor at 150° C. for 30 min. The solvents were evaporated and the crude product was purified by flash chromatography using a gradient of 20% ethyl acetate in hexanes up to 50% to yield 30 mg of 3-methyl-1-[2-(3,4,5-trimethoxy-phenyl)-5H-pyrrolo[2,3-b]pyrazin-7-yl]-butan-1-one. MS: (M+H)+=370, MP=210.0-211.4° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08008298B2
Source datasetuspto-grants-2011_08
ORD IDord-1c93900414dc4600a437dad9b6ec02d0
Source noteuspto-grants-2011_08