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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 573593Generated: October 30, 2026

Potassium Carbonate → Ethyl 4-{[(3-chlorophenyl)sulfonyl]amino}-6-methyl-2-(1H-pyrazol-4-yl)thieno[2,3-b]pyridine-5-carboxylate

https://huagongshe.com/reaction/573593

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant1-tert-Butoxycarbonyl-1H-pyrazole-4-boronic acidHCID 44118675—
ReactantEthyl 2-bromo-4-{[(3-chlorophenyl)sulfonyl]amino}-6-methylthieno[2,3-b]pyridine-5-carboxylateHCID 68323811—
CatalystHCID 178418397HCID 178418397—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Solvent1,4-DioxaneHCID 31275—
ProductEthyl 4-{[(3-chlorophenyl)sulfonyl]amino}-6-methyl-2-(1H-pyrazol-4-yl)thieno[2,3-b]pyridine-5-carboxylateHCID 68380155—

Reaction Conditions

Temperature110 °C

Reaction Steps

A mixture of ethyl 2-bromo-4-{[(3-chlorophenyl)sulfonyl]amino}-6-methylthieno[2,3-b]pyridine-5-carboxylate (Description 72) (402 mg, 0.82 mmol), 1-tert-butoxylcarbonyl-1H-pyrazole-4-boronic acid, pinacol ester (483 mg, 1.64 mmol) and tetrakis(triphenylphosphine)palladium(0) (47.4 mg, 0.041 mmol) and potassium carbonate (340 mg, 2.46 mmol) in 1,4-dioxane (3 mL), DMF (1.5 mL) and water (0.75 mL) was heated at 110° C. for ca. 2 h. After cooling to RT, the reaction mixture was filtered through celite and the filtrate was concentrated. Purification by chromatography on silica, eluting with a gradient of 0-100% ethyl acetate in DCM, afforded the title compound (355 mg). LCMS (A) m/z: 477 [M+1]+, Rt 1.18 min (acidic).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09029545B2
Source datasetuspto-grants-2015_05
ORD IDord-e46268e3b17142e2bbc12cf07b697aa3
Source noteuspto-grants-2015_05