Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2205287Generated: November 1, 2026

Potassium Carbonate → 1-Methyl-1H-pyrazolo[4,3-b]pyridine

https://huagongshe.com/reaction/2205287

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactanttrans-N,N'-dimethyl-1,2-cyclohexanediamineHCID 2733821—
ReactantHCID 117696427HCID 117696427—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
SolventEthyl AcetateHCID 8857—
SolventN-methyl-2-pyrrolidoneHCID 13387—
SolventAmmonium ChlorideHCID 25517—
Product1-Methyl-1H-pyrazolo[4,3-b]pyridineHCID 5697229616.4%

Reaction Conditions

Temperature120 °C

Reaction Steps

N-[1-(3-Bromo-pyridin-2-yl)-methylidene]-N′-methyl-hydrazine (5.7 g, 26.63 mmol), copper (I) iodide (507 mg, 2.66 mmol), trans-N,N′-dimethylcyclohexane-1,2-diamine (76 mg, 0.533 mmol) and potassium carbonate (7.36 g, 53.25 mmol) are suspended in 1-methyl-2-pyrrolidinone (20 mL) and heated at 120° C. for 3 h. The mixture is diluted with saturated ammonium chloride solution and ethyl acetate. The resulting emulsion is filtered, the phases separated and the organic phase washed with brine, dried and volatiles evaporated under reduced pressure. The residue is redissolved in ethyl ether, washed with brine and the solvent removed. The residue is purified by flash chromatography (0-60% EtOAc in cyclohexane) to give 1-methyl-1H-pyrazolo[4,3-b]pyridine (580 mg, content 85%, 14%)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09371282B2
Source datasetuspto-grants-2016_06
ORD IDord-4ddd3f5ba1bf422c8de5cf9678ef3579
Source noteuspto-grants-2016_06