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2-Aminopyridine → 2-(4'-Bromo-biphenyl-4-yl)-imidazo [1,2-a] pyridine
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 2-Aminopyridine | HCID 10439 | — |
| 反応物 | Sodium Bicarbonate | HCID 516892 | — |
| 反応物 | 2-Bromo-1-(4'-bromo-1,1'-biphenyl-4-yl)ethanone | HCID 3274748 | — |
| 溶媒 | Ethanol | HCID 702 | — |
| 生成物 | 2-(4'-Bromo-biphenyl-4-yl)-imidazo [1,2-a] pyridine | HCID 23088534 | 84% |
反応手順
Dissolving 6.7 g (19 mmol) of 2-bromo-1-(4′-bromo-biphenyl-4-yl)-ethanone into 50 milliliter of ethanol, adding 2.1 g (22 mmol) of 2-aminopyridine and 5.0 g of sodium hydrogen carbonate, the resultant suspension was refluxed under heating for 7 hours. After completion of the reaction, separation with filtration was carried out and resultant crystals were washed with water and methanol, thereby obtaining yellow crystals of 2-(4′-bromo-biphenyl-4-yl)-imidazo [1,2-a] pyridine in an amount of 5.5 g (yield: 84%).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07867629B2 |
| 出典データセット | uspto-grants-2011_01 |
| ORD ID | ord-5eef668c5add4ed582770741a23436eb |
| 出典メモ | uspto-grants-2011_01 |