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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1180217Generated: October 31, 2026

Bromine → 3-Bromo-8-fluoroimidazo[1,2-a]pyridine

https://huagongshe.com/reaction/1180217

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromineHCID 24408—
ReactantPotassium BromideHCID 253877—
ReactantSodium AcetateHCID 517045—
Reactant8-Fluoroimidazo(1,2-a)pyridineHCID 11309538—
SolventMethanolHCID 887—
SolventWaterHCID 962—
Product3-Bromo-8-fluoroimidazo[1,2-a]pyridineHCID 3417647683%

Reaction Steps

A solution of bromine in MeOH, saturated with KBr (0.86 M, 1.0 ml, 0.86 mmol) was added to a cooled, stirred solution of 8-fluoroimidazo[1,2-α]pyridine (118 mg, 0.86 mmol) and NaOAc (85 mg, 1.04 mmol) in methanol saturated with KBr (1.6 ml). After 2 min, the solution was poured into water (50 ml) and the resulting yellow solution extracted with CH2Cl2 (3×50 ml). The combined organic fractions were dried over anhydrous Na2SO4 and concentrated in vacuo, yielding 3-bromo-8-fluoroimidazo[1,2-α]pyridine as a yellow solid (155 mg, 83%), used without further purification: δH (400 MHz, CDCl3) 6.86-6.91 (1H, m), 6.95-6.99 (1H, m), 7.65 (1H, s), 7.98 (1H, dd, J 0.8 and 6.7); m/z (ES+) 217 (100%, [MH]+), 215 (100).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07279580B2
Source datasetuspto-grants-2007_10
ORD IDord-19233aec091d4b7780094a08a8155392
Source noteuspto-grants-2007_10