HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2192690Generated: November 2, 2026
Ethyl Acetate → 1-(6-Pyridin-4-ylpyrazin-2-yl)-1H-benzimidazol-6-amine
https://huagongshe.com/reaction/2192690
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 1-(6-chloropyrazin-2-yl)-1H-benzimidazol-6-amine | HCID 58217094 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | HCID 22495535 | HCID 22495535 | — |
| Product | 1-(6-Pyridin-4-ylpyrazin-2-yl)-1H-benzimidazol-6-amine | HCID 58217161 | — |
Reaction Steps
Under a nitrogen atmosphere a mixture of 1-(6-chloropyrazin-2-yl)-1H-benzimidazol-6-amine (50 mg, 0.20 mmol), 4-pyridylboronic add (30 mg, 0.24 mmol), tetrakis(triphenylphosphine)palladium(0) (23 mg, 0.02 mmol) in toluene-n-propanol (2 mL, 3:1) was treated with 2M aqueous sodium carbonate solution (0.14 mL, 0.84 mmol). The resulting mixture was stirred vigorously whilst being heated under reflux overnight. Upon cooling, the mixture was diluted with ethyl acetate (10 mL) and washed with H2O (1×10 mL). The aqueous phase was extracted with ethyl acetate (10 mL) and the organic layers combined and washed with 0.5M Na2CO3, brine and then dried (Na2SO4). Removal of solvent fit vacuo then yielded crude product, which was purified by column chromatography using dichloromethane-methanol (98:2-91:9) as eluent to furnish the product (32 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08329737B2 |
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| Source dataset | uspto-grants-2012_12 |
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| ORD ID | ord-b1dacd5d79e947fcb784914733abbeb1 |
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| Source note | uspto-grants-2012_12 |
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