Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzamidine | HCID 2332 | — |
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Product | HCID 178420139 | HCID 178420139 | 72% |
Reaction Steps
2-Bromo-1-(pyrindin-4-yl)ethanone hydrobromide (6.4 g, 23 mmol) was added portionwise to a solution of benzamidine (11.2 g, 93 mmol) in dry DMF (50 mL) at 0° C., maintaining an internal temperature of <5° C. The stirred reaction was allowed to warm to rt over 2 h and then heated to 40° C. for 16 h. The crude reaction was poured into saturated aqueous NaHCO3 solution (600 mL), and partition and extracted with EtOAc (3×300 mL). The combined organic layers were dried (Na2SO4) and evaporated. The resulting crude residue was purified by flash chromatography (SiO2, 100:0-90:10 DCM-MeOH) to give 3.68 g (72%) of 4-(2-phenyl-1H-imidazol-4-yl)pyridine: 1H NMR (CDCl3) δ 9.73 (broad s, 1H), 8.61 (d, J=6.0, 1.2 Hz, 2H), 7.91 (d, J=8.0, 1.6 Hz, 2H), 7.77 (d, J=6.0, 1.2 Hz, 2H), 7.57 (s, 1H), 7.48 (m, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08865732B2 |
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| Source dataset | uspto-grants-2014_10 |
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| ORD ID | ord-1c538f6dd9654cb59ff44add4d95b061 |
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| Source note | uspto-grants-2014_10 |
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