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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2359920Generated: October 26, 2026

6-Bromopyridine-2-sulfonamide → 6-[1-(pyridin-3-yl)-1H-pyrazol-4-yl]pyridine-2-sulphonamide

https://huagongshe.com/reaction/2359920

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6-Bromopyridine-2-sulfonamideHCID 57345816—
Reactant3-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazol-1-yl)pyridineHCID 57416218—
CatalystHCID 178418397HCID 178418397—
Product6-[1-(pyridin-3-yl)-1H-pyrazol-4-yl]pyridine-2-sulphonamideHCID 66633631—

Reaction Conditions

Temperature70 °C

Reaction Steps

Under argon, 3-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazol-1-yl]pyridine (0.2 g, 0.74 mmol, prepared by the methods described in WO 2011/045224), 6-bromopyridin-2-sulphonamide (0.175 g, 0.74 mmol) and tetrakis(triphenylphosphine)palladium (0.025 g, 0.022 mmol) were added to a mixture, degassed by means of argon, of sodium carbonate solution in water (2.9 ml, 2 M/L) and acetonitrile (4 ml). The reaction mixture was stirred at 70° C. for 18 h. After cooling, the reaction mixture was poured onto water and the precipitated crystals were filtered off with suction. They were subsequently stirred with diethyl ether and filtered off with suction. This gave 0.23 g (97% of theory) of 6-[1-(pyridin-3-yl)-1H-pyrazol-4-yl]pyridine-2-sulphonamide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08686004B2
Source datasetuspto-grants-2014_04
ORD IDord-a29f05021e9442229f8ad18f739e5945
Source noteuspto-grants-2014_04