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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1374696Generated: October 30, 2026

Water → 2-(4-Fluorophenyl)-3-bromopyrazolo[1,5-a]pyridine

https://huagongshe.com/reaction/1374696

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantN-bromobutanimideHCID 67184—
ReactantSodium BicarbonateHCID 516892—
Reactant2-(4-Fluorophenyl)pyrazolo[1,5-A]pyridine-3-carboxylic acidHCID 21948681—
SolventDimethylformamideHCID 6228—
Product2-(4-Fluorophenyl)-3-bromopyrazolo[1,5-a]pyridineHCID 21948678—

Reaction Steps

To a solution of 2-(4-fluorophenyl)-pyrazolo[1,5-a]pyridine-3-carboxylic acid (0.96 g, 3.75 mmol) in dry DMF (10 mL) was added sodium bicarbonate (0.95 g, 11.3 mmol) followed by N-bromosuccinimide (0.667 g, 3.75 mmol) and the mixture was stirred at room temperature under a nitrogen atmosphere for about 90 min. The mixture was poured into water (300 mL) and the resulting solid was collected by filtration and washed with water. The solid was dissolved in 10:1 chloroform:methanol (10 mL) and filtered through a pad (0.5 cm) of silica gel using 10:1 chloroform:methanol as eluent. The filtrate was evaporated to leave the title compound as a tan solid, 0.87 g (80%). 1H NMR (d6-DMSO) δ 8.7 (d, 1H, J=6.9 Hz), 8.02 (dd, 2H, J=8.7, 5.7 Hz), 7.61 (d, 1H, J=8.4 Hz), 7.40 (t, 1H, J=6 Hz), 7.38 (t, 2H, J=9 Hz), 7.04 (t, 1H, J=6.9 Hz). MS (+ve ion electrospray) 293 (100), (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07166597B2
Source datasetuspto-grants-2007_01
ORD IDord-285e683ca57e4b3b9a5171555b04cfac
Source noteuspto-grants-2007_01