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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1162467Generated: October 28, 2026

Bromide ion → HCID 57749423, compound

https://huagongshe.com/reaction/1162467

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromide ionHCID 259—
Reactant2-FluoropyridineHCID 9746—
ReactantCesium carbonateHCID 10796—
ReactantHCID 178508148HCID 178508148—
SolventWaterHCID 962—
SolventDimethylacetamideHCID 31374—
ProductHCID 57749423HCID 5774942326%

Reaction Conditions

Temperature150 °C

Reaction Steps

To two 10-20 mL microwave vials was added 5-bromo-1H-benzo[d]imidazol-2-amine (3.00 g, 14.1 mmol, Carbocore, The Woodlands, Tex.), N,N-dimethylacetamide (20 mL), 2-fluoropyridine (1.46 mL, 17.0 mmol, Aldrich, St. Louis, Mo.) and cesium carbonate (7.84 g, 24.1 mmol). (One-half of the material in each vial, ie 1.5 g of the bromide in each vial.) The mixture was heated at 150° C. for 140 min in the microwave. After cooling to rt, the combined reaction mixtures were poured into water (400 mL) and then extracted with EtOAc/hexane (80:20) (3×150 mL). The combined extracts were washed with water (3×100 mL) and brine (100 mL) and then dried (Na2SO4) and concentrated onto silica. Purification by silica gel chromatography (0.5 to 3.8% MeOH (2 M in NH3)/CH2Cl2) afforded the title compound (1.06 g, 26%). MS (ESI, positive ion) m/z: 289 (M(79Br)+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07820665B2
Source datasetuspto-grants-2010_10
ORD IDord-b030045f6cac40fc9fb56e437aabc5df
Source noteuspto-grants-2010_10