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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 573683Generated: October 30, 2026

Potassium Carbonate → HCID 68324151, compound

https://huagongshe.com/reaction/573683

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant1,4-DioxaneHCID 31275—
Reactant3-Methoxy-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridineHCID 3866161—
Reactant1,1-Dimethylethyl 4-(3-bromo-4-{[(3-chlorophenyl)sulfonyl]amino}-6-methylthieno[2,3-b]pyridin-2-yl)-1H-pyrazole-1-carboxylateHCID 68324029—
CatalystHCID 178418397HCID 178418397—
CatalystHCID 178418476HCID 178418476—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 68324151HCID 68324151108.5%

Reaction Conditions

Temperature110 °C

Reaction Steps

A mixture of 1,1-dimethylethyl 4-(3-bromo-4-{[(3-chlorophenyl)sulfonyl]amino}-6-methylthieno[2,3-b]pyridin-2-yl)-1H-pyrazole-1-carboxylate (Description 75) (100 mg, 0.171 mmol), 3-methoxy-5-pyridineboronic acid pinacol ester (81 mg, 0.343 mmol), potassium carbonate (71.0 mg, 0.514 mmol), tetrakis(triphenylphosphine)palladium(0) (4.95 mg, 4.28 μmol) and bis(triphenylphosphine)palladium(II) chloride (3.01 mg, 4.28 μmol) were weighed into a microwave vial. 1,4-Dioxane (1.5 mL), DMF (0.75 mL) and water (0.38 mL) were added and the mixture heated in a microwave at 110° C. for 30 min. At this point, both reaction mixtures were combined and concentrated. The residue was passed through an SCX cartridge, eluting with MeOH (100 mL) and then 2M NH3 in MeOH (150 mL). The basic methanolic solution was concentrated and purified by MDAP (acidic conditions), to give the title compound (95 mg). LCMS (A) m/z: 512 [M+1]+, Rt 0.88 min (acidic).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09029545B2
Source datasetuspto-grants-2015_05
ORD IDord-fe8ecb8d6464426faef4ee8e6ba1b862
Source noteuspto-grants-2015_05