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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Benzimidazole | HCID 5798 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 5-Bromo-2,4-dichloropyrimidine | HCID 289973 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 2-(Benzimidazol-1-yl)-4-chloro-5-bromopyrimidine | HCID 18354392 | — |
| Product | HCID 22731922 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06316444B1 |
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| Source dataset | uspto-grants-2001_11 |
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| ORD ID | ord-c6daac7d60384014849b46a1eae44d98 |
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| Source note | uspto-grants-2001_11 |
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