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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2197240Generated: October 30, 2026

Potassium Carbonate → HCID 66974560, compound

https://huagongshe.com/reaction/2197240

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantMethylboronic AcidHCID 139377—
ReactantSodium BicarbonateHCID 516892—
ReactantHydrogen chloride-ethyl acetateHCID 21866389—
ReactantHCID 66974640HCID 66974640—
CatalystHCID 178418397HCID 178418397—
SolventEthanolHCID 702—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 66974560HCID 6697456039%

Reaction Conditions

Temperature80 °C

Reaction Steps

Under an argon atmosphere, a mixture of tert-butyl({1-[(5-bromopyridin-3-yl)sulfonyl]-5-phenyl-1H-pyrrol-3-yl}methyl)methylcarbamate (112 mg), methylboronic acid (18 mg), tetrakis(triphenylphosphine)palladium (23 mg), potassium carbonate (138 mg) and 1,4-dioxane (5 mL) was stirred at 80° C. for one day. The reaction mixture was poured into a saturated aqueous sodium hydrogencarbonate solution, and the mixture was extracted with ethyl acetate. The extract was washed with saturated brine, dried over magnesium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (eluent: hexane-ethyl acetate=19:1→1:1) to give an oil. The oil was dissolved in ethanol (1 mL), and a 4 mol/L hydrogen chloride-ethyl acetate solution (1 mL) was added. After stirring at room temperature for 1 hr, the mixture was concentrated under reduced pressure. The residue was recrystallized from ethanol-ethyl acetate to give the title compound as a colorless solid (yield 32.6 mg, 39%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08338462B2
Source datasetuspto-grants-2012_12
ORD IDord-acfb1da483f7475cadcfce73eb86cb71
Source noteuspto-grants-2012_12