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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2206241Generated: November 2, 2026

Benzyl Bromide → 1-benzyl-4-chloro-3-iodo-1H-pyrazolo[4,3-c]pyridine

https://huagongshe.com/reaction/2206241

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantPotassium HydroxideHCID 14797—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 178478341HCID 178478341—
SolventDimethylformamideHCID 6228—
Product1-benzyl-4-chloro-3-iodo-1H-pyrazolo[4,3-c]pyridineHCID 11798799160%

Reaction Steps

To a mixture of 4-chloro-3-iodo-1H-pyrazolo[4,3-c]pyridine (6.3 g) and potassium hydroxide (2.5 g) in DMF (60 mL) was added benzyl bromide (4.6 g) at room temperature. The reaction mixture was stirred at room temperature for 4 hr. The reaction mixture was neutralized with saturated aqueous sodium hydrogencarbonate solution under ice-cooling, and the mixture was extracted with ethyl acetate. The organic layer was washed with water and saturated brine, dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate/petroleum ether) to give the title compound (5.0 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09371320B2
Source datasetuspto-grants-2016_06
ORD IDord-9e7b0c5a580340469a01ca6ecef8c7ee
Source noteuspto-grants-2016_06