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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1952289Generated: November 1, 2026

Sodium Bicarbonate → 5-[4-(4-Pyridinyl)-6-quinolinyl]-3-pyridinesulfonamide

https://huagongshe.com/reaction/1952289

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium BicarbonateHCID 516892—
Reactant5-Bromopyridine-3-sulfonamideHCID 12684258—
Reactant4-(4-Pyridinyl)-6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)quinolineHCID 66782374—
Solvent1,4-DioxaneHCID 31275—
Product5-[4-(4-Pyridinyl)-6-quinolinyl]-3-pyridinesulfonamideHCID 25121265—

Reaction Conditions

Temperature120 °C

Reaction Steps

A mixture of 4-(4-pyridinyl)-6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)quinoline (250 mg, 0.75 mmol), 5-bromopyridine-3-sulfonamide (213 mg, 0.9 mmol), tetrakistriphenylphosphine palladium (0) (95 mg, 0.08 mmol), and saturated aqueous NaHCO3 (2.5 mL), and dioxane (5 mL)) was heated at 120° C. for 1 h and cooled to room temperature. The reaction mixture was filtered through Celite and the solvent was removed under reduced pressure. The crude product was purified by Gilson reverse phase HPLC (8-25% 6 min gradient 0.1% TFA in H2O/CH3CN) followed by neutralization with saturated aqueous NaHCO3 and extracted into EtOAc. Evaporation provided the title compound as an off white solid. (85 mg, 31%). ESMS [M+H]+=363.1

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08404837B2
Source datasetuspto-grants-2013_03
ORD IDord-eb1aa83651f64b6ca17bb12e35739b8c
Source noteuspto-grants-2013_03