Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1035833Generated: October 30, 2026

Sodium Carbonate → N-(3-((5-(4-cyanophenyl)thiazol-2-yl)amino)phenyl)methanesulfonamide

https://huagongshe.com/reaction/1035833

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
ReactantLithium ChlorideHCID 433294—
Reactant4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)benzonitrileHCID 2734625—
ReactantN-(3-((5-bromothiazol-2-yl)amino)phenyl)methanesulfonamideHCID 86674186—
CatalystHCID 178418397HCID 178418397—
SolventHexaneHCID 8058—
ProductN-(3-((5-(4-cyanophenyl)thiazol-2-yl)amino)phenyl)methanesulfonamideHCID 7147199789%

Reaction Conditions

Temperature100 °C

Reaction Steps

To a mixture of N-(3-((5-bromothiazol-2-yl)amino)phenyl)methanesulfonamide 56 (0.159 g, 0.458 mmol), commercially available 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzonitrile 57 (0.125 g, 0.545 mmol), Lithium chloride (0.038 g, 0.916 mmol) and tetrakis(triphenylphosphine)palladium (0.058 g, 0.05 mmol) in dry and degassed (using argon) 1,4-Dioxane (20 mL) was added aq. Na2CO3 (1M, 0.91 mL, 0.916 mmol). Reaction mixture was degassed again for 2-3 times for 10 minutes and resulting yellow mixture was stirred under argon at 100° C. for 14 hours. Reaction mixture was filtered through a small pad of celite and concentrated. Crude product was MPLC (Biotage) silica column chromatographed using Acetone:Hexane as an eluent to obtain N-(3-((5-(4-cyanophenyl)thiazol-2-yl)amino)phenyl)methanesulfonamide 58 (0.15 g, 89% yield). MS (ES) m/z 371 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08546400B2
Source datasetuspto-grants-2013_10
ORD IDord-32ce15be68bb4a8cbe691c622fa9e14e
Source noteuspto-grants-2013_10