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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1797044Generated: November 3, 2026

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

https://huagongshe.com/reaction/1797044

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-(4fluorophenyl)-pyrazolo[1,5-a]pyridine-3-carboxylic acid (0.96 g, 3.75 mmol) in dry N,N-dimethylformamide (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 minutes. 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 numberUS07034030B2
Source datasetuspto-grants-2006_04
ORD IDord-c127b49911a14475b37f7cb24bb8dfc6
Source noteuspto-grants-2006_04