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Acetonitrile → N-phenyl-6-(pyrid-3-yl)imidazo[1,2-a]pyridine-2-carboxamide
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Acetonitrile | HCID 6342 | — |
| 反応物 | Sodium Carbonate | HCID 10340 | — |
| 反応物 | 3-Pyridinylboronic acid | HCID 2734378 | — |
| 反応物 | 6-bromo-N-phenylimidazo[1,2-a]pyridine-2-carboxamide | HCID 24771673 | — |
| 触媒 | HCID 178418397 | HCID 178418397 | — |
| 溶媒 | Toluene | HCID 1140 | — |
| 生成物 | N-phenyl-6-(pyrid-3-yl)imidazo[1,2-a]pyridine-2-carboxamide | HCID 44137633 | 48.9% |
反応手順
150 mg of 6-bromo-N-phenylimidazo[1,2-a]pyridine-2-carboxamide (Intermediate 1), 0.237 g of pyridine-3-boronic acid, 45 mg of tetrakis(triphenylphosphine)palladium, 2 mL of aqueous 2M sodium carbonate solution, 4 mL of acetonitrile and 4 mL of toluene are placed in a microwave tube. The mixture is heated for 20 minutes in a microwave machine set at 150° C., and then cooled and filtered, the insoluble matter being washed with a mixture of methanol and dichloromethane. The combined filtrates are concentrated to dryness under reduced pressure. The residue is concreted with aqueous methanol to give 73 mg of N-phenyl-6-(pyrid-3-yl)imidazo[1,2-a]pyridine-2-carboxamide in the form of an off-white solid.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US08314109B2 |
| 出典データセット | uspto-grants-2012_11 |
| ORD ID | ord-4b02cd74bd674f53bf290ff6610a4748 |
| 出典メモ | uspto-grants-2012_11 |