HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetonitrile → [3-(2-(Benzofuran-3-yl)imidazo[1,2-a]pyridin-6-yl)phenyl]methanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | [3-(Hydroxymethyl)phenyl]boronic acid | HCID 2734662 | — |
| Reactant | 2-(Benzofuran-3-yl)-6-bromoimidazo[1,2-a]pyridine | HCID 68640089 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | [3-(2-(Benzofuran-3-yl)imidazo[1,2-a]pyridin-6-yl)phenyl]methanol | HCID 68639346 | 40.5% |
Reaction Steps
100 mg of 2-(benzofuran-3-yl)-6-bromoimidazo[1,2-a]pyridine, 73 mg of 3-(hydroxymethyl)phenylboronic acid and 11 mg of tetrakis(triphenylphosphine)palladium are placed in a microwave tube. 2 ml of acetonitrile, 2 ml of toluene and 1.5 ml of a 2M solution of sodium carbonate are added thereto. The tube is placed in a microwave device and irradiated at 150° C. for 15 min. The organic phase is separated, dried, and then concentrated under reduced pressure. The oily residue is taken up with 3 ml of dichloromethane and triturated for 1 hour. The precipitate is recovered by filtration, washed with diisopropyl ether and dried in a desiccator under reduced pressure. 44 mg of compound are obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08338451B2 |
| Source dataset | uspto-grants-2012_12 |
| ORD ID | ord-b75160df44a144d4bb3017dd0491e04f |
| Source note | uspto-grants-2012_12 |