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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1802889Generated: October 26, 2026

N,N'-Dimethylethylenediamine → 4-(cyclopropylsulfonyl)-1H-pyrazolo[3,4-b]pyridine

https://huagongshe.com/reaction/1802889

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN,N'-DimethylethylenediamineHCID 8070—
ReactantPotassium CarbonateHCID 11430—
ReactantSodium cyclopropanesulfinateHCID 42643363—
Reactant4-Iodo-1H-pyrazolo[3,4-b]pyridineHCID 57642801—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
SolventDimethyl SulfoxideHCID 679—
Product4-(cyclopropylsulfonyl)-1H-pyrazolo[3,4-b]pyridineHCID 579641099%

Reaction Conditions

Temperature100 °C

Reaction Steps

To a solution of 4-iodo-1H-pyrazolo[3,4-b]pyridine (5.2 g) in dimethyl sulfoxide (70 mL) were added N,N′-dimethylethylenediamine (114 μL), copper (I) iodide (202 mg), sodium cyclopropanesulfinate (8.16 g) and potassium carbonate (5.06 g) at room temperature under argon atmosphere, and the mixture was stirred at 100° C. for 16 hr. The reaction mixture was filtered, water was added to the filtrate, and the mixture was extracted with ethyl acetate. The ethyl acetate layer was washed with saturated brine, dried (MgSO4), and concentrated. The obtained residue was subjected to silica gel column chromatography to give the title compound (0.42 g, yield 9%) as yellow crystals from the fraction eluted with ethyl acetate-hexane (1:1, volume ratio). MS: 224 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08349886B2
Source datasetuspto-grants-2013_01
ORD IDord-0a58d9542a994a4c8bc0e0482c449355
Source noteuspto-grants-2013_01