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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1809189Generated: October 30, 2026

Water → HCID 135998255, compound

https://huagongshe.com/reaction/1809189

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium CarbonateHCID 11430—
Reactant4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenolHCID 2734624—
ReactantBis[2-(diphenylphosphino)phenyl] etherHCID 4285986—
ReactantHCID 58337113HCID 58337113—
Catalystpalladium(II) acetateHCID 167845—
SolventDimethylformamideHCID 6228—
ProductHCID 135998255HCID 135998255—

Reaction Conditions

Temperature88 °C

Reaction Steps

A mixture of 4-[(3-Bromo-5-methyl-imidazo[1,2-a]pyrazin-8-ylamino)-methyl]-benzenesulfonamide (0.1 g, 0.252 mmol), 4-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-phenol (0.061 g, 0.277 mmol), K2CO3 1.5M in water (0.34 mL, 0.504 mmol), Pd(OAc)2 (3.0 mg, 0.013 mmol), and (oxidi-2,1-phenylene)bis(diphenylphosphine) (14 mg, 0.026 mmol) in DMF 1 mL is stirred at 88° C. overnight. The reaction mixture is filtered through cotton, diluted with AcOEt, washed with water, the organic layer dried with MgSO4 anh. filtered and evaporated. The crude mixture is purified by prep. HPLC under acid conditions using a gradient of 0.1% formic acid in H2O/0.1% formic acid in Acetonitrile (95/5:5 min, 9/1:13 min, 0/1:4 min) to give 4-{[3-(4-hydroxy-phenyl)-5-methyl-imidazo[1,2-a]pyrazin-8-ylamino]-methyl}-benzenesulfonamide as a brown oil, (36.5 mg) LC-MS m/z 410 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08362018B2
Source datasetuspto-grants-2013_01
ORD IDord-88e8c2b4dc014d4996ba1b2a72b3c34f
Source noteuspto-grants-2013_01