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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1186790Generated: November 1, 2026

Dichloromethane → 1-(3-Sulfamoylphenyl)-1H-pyrazolo[3,4-b]pyridin-4-ylboronic acid

https://huagongshe.com/reaction/1186790

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantPotassium AcetateHCID 517044—
ReactantBis(pinacolato)diboraneHCID 2733548—
Reactant3-(4-iodo-1H-pyrazolo[3,4-b]pyridin-1-yl)benzenesulfonamideHCID 66664861—
SolventDimethyl SulfoxideHCID 679—
Product1-(3-Sulfamoylphenyl)-1H-pyrazolo[3,4-b]pyridin-4-ylboronic acidHCID 66668003—

Reaction Conditions

Temperature84 °C

Reaction Steps

To a 48 mL pressure bottle was added 3-(4-iodo-1H-pyrazolo[3,4-b]pyridin-1-yl)benzenesulfonamide, “dot” 2 1-methyl-2-pyrrolidinone complex (60 mg, 0.100 mmol), 4,4,4′,4′,5,5,5′,5′-octamethyl-2,2′-bi(1,3,2-dioxaborolane) (94.7 mg, 0.373 mmol), potassium acetate (24.4 mg, 0.249 mmol) and anhydrous DMSO (Volume: 2 mL). The reaction mixture was purged well with argon and treated with PdCl2(dppf).CH2Cl2 (12.5 mg, 0.017 mmol). The reaction mixture was then heated to 84° C. for 1 h to give the desired intermediate. LC/MS (Condition B): ret. T=2.4 min, (M+H)+ 318.98.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08673922B2
Source datasetuspto-grants-2014_03
ORD IDord-1e76399b7ba24a718af6a74a4c700551
Source noteuspto-grants-2014_03