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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 218206Generated: October 30, 2026

Morpholine → N-(4-Chloro-2-[1,2,3]triazolo[4,5-b]pyridin-1-yl-phenyl)-3-fluoro-4-morpholin-4-yl-benzenesulfonamide

https://huagongshe.com/reaction/218206

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMorpholineHCID 8083—
ReactantPotassium phosphate, tribasic, monohydrateHCID 22031701—
ReactantHCID 59428112HCID 59428112—
CatalystTris(dibenzylideneacetone) dipalladiumHCID 9832798—
SolventDimethylformamideHCID 6228—
ProductN-(4-Chloro-2-[1,2,3]triazolo[4,5-b]pyridin-1-yl-phenyl)-3-fluoro-4-morpholin-4-yl-benzenesulfonamideHCID 2513439844.2%

Reaction Steps

4-Bromo-N-(4-chloro-2-[1,2,3]triazolo[4,5-b]pyridin-1-yl-phenyl)-3-fluoro-benzensulfonamide (synthesized according to general procedure G, 180 mg, 0.37 mmol) was dissolved in 3 ml of anhydrous dimethylformamide under an atmosphere of nitrogen. To this mixture was added morpholine (161 mg, 1.85 mmol), 2,2′-bis(diphenylphosphine)-1,1′-binaphthyl (BINAP) (34 mg, 0.055 mmol), potassium phosphate tribasic monohydrate (511 mg, 2.22 mmol), and tris(dibenzylideneacetone) dipalladium(0) (Pd2(dba)3) and the resultant mixture was heated at 80° C. overnight. The following day, the reaction mixture was partitioned with a saturated solution of sodium bicarbonate and dichloromethane and the aqueous layer was extracted three times with dichloromethane. The combined organics were subsequently dried over magnesium sulfate, concentrated in vacuo, and purified by reverse phase HPLC, followed by silica gel chromatography employing ethyl acetate:hexanes (1:1), to afford 80 mg of the desired product as a white powder: MS (ES) M+H expected 489.1, found 489.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08198309B2
Source datasetuspto-grants-2012_06
ORD IDord-7626c644499c4338a1dd06ea6956c4c2
Source noteuspto-grants-2012_06