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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1361118Generated: October 30, 2026

Potassium Carbonate → 4-Bromo-1-(4-fluorophenyl)-1H-pyrazolo[3,4-c]pyridine

https://huagongshe.com/reaction/1361118

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantN-[(E)-(3,5-dibromo-4-pyridinyl)methylideneamino]-4-fluoroanilineHCID 59278325—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
SolventN-methyl-2-pyrrolidoneHCID 13387—
SolventAmmonium ChlorideHCID 25517—
Product4-Bromo-1-(4-fluorophenyl)-1H-pyrazolo[3,4-c]pyridineHCID 59278460—

Reaction Conditions

Temperature120 °C

Reaction Steps

A mixture of N-[1-(3,5-dibromopyridin-4-yl)-meth-(E)-ylidene]-N′-(4-fluorophenyl)-hydrazine (2.0 g, 5.4 mmol), CuI (50.0 mg, 0.260 mmol), trans-N,N′-dimethylcyuclohexane-1,2-diamine (0.200 mL, 1.27 mmol), and K2CO3 (1.4 g, 0.010 mol) in NMP (10 mL) was warmed at 120° C. for 30 minutes. The reaction was monitored by HPLC-MS indicating the desired mass. The mixture was diluted with aqueous ammonium chloride (100 mL) and the resulting solid collected by filtration. The solid was dissolved in hot ethyl acetate (EtOAc), dried over magnesium sulfate, treated with activated carbon, filtered through diatomaceous earth and concentrated. The residue was passed through a pad of silica gel eluting with dichloromethane to afford 4-bromo-1-(4-fluorophenyl)-1H-pyrazolo[3,4-c]pyridine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07879873B2
Source datasetuspto-grants-2011_02
ORD IDord-8c73be6178ad47e59579dba6e3aeb066
Source noteuspto-grants-2011_02