Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Chloride | HCID 5234 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1-Ethynyl-4-fluorobenzene | HCID 522627 | — |
| Reactant | HCID 118195059 | HCID 118195059 | — |
| Catalyst | Copper iodide | HCID 83717 | — |
| Catalyst | Bis(dibenzylideneacetone)palladium | HCID 9811564 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 73051807 | HCID 73051807 | 88.9% |
Reaction Steps
In a flask placed under an argon flow, 2 g (3.82 mmol) of methyl 2-((3-iodoimidazo[1,2-a]pyridin-2-yl)methoxy)benzoate were dissolved in 8 ml of dimethylformamide with magnetic stirring. To this solution were added: 0.074 g (0.382 mmol) of copper iodide, 0.551 g (4.59 mmol) of 1-ethynyl-4-fluorobenzene and 8 ml (57.3 mmol) of triethylamine. The reaction medium was degassed with argon for 10 min before adding 0.35 g (0.382 mmol) of Pd2(dba)3. The mixture was stirred at r.t. for 16 h before being treated with 100 ml of a saturated NaCl aqueous solution. The aqueous phase was extracted with 2×100 ml of ethyl acetate. The combined organic phases were washed with 100 ml of a saturated NaCl aqueous solution, dried on Na2SO4 which was then removed by filtration. The obtained filtrate was concentrated in vacuo. The crude residue was purified by flash chromatography on a silica gel cartridge (eluent: heptane/ethyl acetate, 1/1, v/v). 1.36 g (yield=84%) of methyl 2-((3-((4-fluorophenyl)ethynyl) imidazo[1,2-a]pyridin-2-yl)methoxy)benzoate were obtained as a pale brown solid. LC-MS: m/z=401 (MH+); UV purity at 254 nm=98%. 1H NMR (300 MHz, DMSO) δ 8.63 (d, J=6.7 Hz, 1H), 7.75-7.59 (m, 4H), 7.48 (ddd, J=15.9, 11.5, 4.8 Hz, 2H), 7.40-7.26 (m, 3H), 7.13 (t, J=6.8 Hz, 1H), 7.01 (t, J=7.4 Hz, 1H), 5.40 (s, 2H), 3.68 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09381191B2 |
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| Source dataset | uspto-grants-2016_07 |
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| ORD ID | ord-d734f3e4c1b74ae893a151712cc8642d |
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| Source note | uspto-grants-2016_07 |
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