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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 429286Generated: October 29, 2026

Benzimidazole → 2-(Benzimidazol-1-yl)-4-chloro-5-bromopyrimidine

https://huagongshe.com/reaction/429286

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzimidazoleHCID 5798—
ReactantSodium hydrideHCID 24758—
Reactant5-Bromo-2,4-dichloropyrimidineHCID 289973—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product2-(Benzimidazol-1-yl)-4-chloro-5-bromopyrimidineHCID 18354392—
ProductHCID 22731922HCID 22731922—

Reaction Steps

To a suspension of NaH (23 mg) in 1.5 mL of DMF was added benzimidazole (111 mg). After gas evolution ceased, the mixture was stirred at room temperature for 10 min, then added to a solution of 2,4-dichloro-5-bromopyrimidine (178 mg) in 1 mL of DMF. The mixture was stirred for 3 h at room temperature, then diluted with 10 mL of EtOAc and quenched with 5 mL of water. The phases were separated and the organic phase was washed with 5 mL of water and 5 mL of brine, then dried over Na2SO4 and concentrated. The residue was purified by flash chromatography, eluting with 4:1 hexanes-acetone to provide 151 mg of the title compound (polar isomer) and 15 mg of the regioisomer 2-(benzimidazol-1-yl)-4-chloro-5-bromopyrimidine (nonpolar isomer). Mass spectrum (ESI) 310.9 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06316444B1
Source datasetuspto-grants-2001_11
ORD IDord-c6daac7d60384014849b46a1eae44d98
Source noteuspto-grants-2001_11