HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 656399Generated: October 26, 2026
2-Bromopyridine → tert-Butyl (2-oxo-3-pyridin-2-yl-2,3-dihydro-1H-benzimidazol-1-yl)acetate
https://huagongshe.com/reaction/656399
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-Bromopyridine | HCID 7973 | — |
| Reactant | Potassium Acetate | HCID 517044 | — |
| Reactant | Tert-butyl (2-oxo-2,3-dihydrobenzimidazol-1-yl)acetate | HCID 20814117 | — |
| Catalyst | Copper | HCID 23978 | — |
| Catalyst | Cuprous chloride | HCID 62652 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | tert-Butyl (2-oxo-3-pyridin-2-yl-2,3-dihydro-1H-benzimidazol-1-yl)acetate | HCID 86607780 | — |
Reaction Steps
A mixture of tert-butyl (2-oxo-2,3-dihydro-1H-benzimidazol-1-yl)acetate from Step A (1.75 g, 7.05 mmol), 2-bromopyridine (3.36 mL, 35.2 mmol), copper powder (1.57 g, 24.7 mmol), CuCl (140 mg, 1.41 mmol), and KOAc (2.08 g, 21.1 mmol) in pyridine (30 mL) was heated at 100° C. for 3 h. The cooled mixture was partitioned between EtOAc (150 mL) and 10% aqueous citric acid (100 mL) and the organic layer was dried over Na2SO4, filtered, and concentrated under reduced pressure. The crude product was purified by silica gel chromatography, eluting with a gradient of hexane:EtOAc—100:0 to 0:100, to give the title compound. MS: m/z=326 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08071771B2 |
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| Source dataset | uspto-grants-2011_12 |
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| ORD ID | ord-632af1b1ce7c4470878b675b602e97e1 |
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| Source note | uspto-grants-2011_12 |
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