Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2083902Generated: October 31, 2026

Benzimidazole → HCID 22731922, compound

https://huagongshe.com/reaction/2083902

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzimidazoleHCID 5798—
ReactantEthyl AcetateHCID 8857—
ReactantSodium hydrideHCID 24758—
Reactant5-Bromo-2,4-dichloropyrimidineHCID 289973—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 22731922HCID 2273192264.6%

Reaction Conditions

Temperature0 °C

Reaction Steps

Sodium hydride (60% dispersion in oil; 110 mg, 2.75 mmol) was added to a solution of benzimidazole (295 mg, 2.5 mmol) in DMF (6 ml) at 0° C. The mixture was stirred at 0° C. for 10 minutes and then added dropwise to a cold (0° C.) solution of 5-bromo-2,4-dichloropyrimidine (712 mg, 3.14 mmol) in DMF (6 ml). The mixture was stirred for at 0° C. for 2 hours and then ethyl acetate (20 ml) and water (20 ml) were added. The organic phase was separated and dried and volatile material was removed by evaporation. The residue was purified by column chromatography, eluting with 20% ethyl acetate/DCM, to give the product as a white solid (500 mg, 52%). NMR: 7.4 (m, 2H), 7.8 (m, 2H), 8.8 (s, 1H), 9.3 (s, 1H); MS (MH+): 309, 311.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06716831B1
Source datasetuspto-grants-2004_04
ORD IDord-bbb9f9b599e94bc3b7034752dc086bb6
Source noteuspto-grants-2004_04