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Diisopropyl Ether → Methyl 3-(1-bromonaphthalen-2-ylmethyl)-2,7-dimethyl-3H-imidazo[4,5-b]pyridine-5-carboxylate
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Diisopropyl Ether | HCID 7914 | — |
| 反応物 | Sodium hydride | HCID 24758 | — |
| 反応物 | 1-Bromo-2-(bromomethyl)naphthalene | HCID 37828 | — |
| 反応物 | methyl 2,7-dimethyl-3H-imidazo[4,5-b]pyridine-5-carboxylate | HCID 22388027 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 生成物 | Methyl 3-(1-bromonaphthalen-2-ylmethyl)-2,7-dimethyl-3H-imidazo[4,5-b]pyridine-5-carboxylate | HCID 22388177 | 104.5% |
反応手順
To a suspension of methyl 2,7-dimethyl-1H-imidazo[4,5-b]pyridine-5-carboxylate (625 mg) in N,N-dimethylformamide (6 ml) was added sodium hydride (70% in mineral oil, 125 mg) under ice-cooling, and the mixture was stirred for 30 min. 1-Bromonaphthalen-2-ylmethyl bromide (1.05 g) was added to the reaction mixture, and the mixture was stirred under ice-cooling for 3 hr. Diisopropyl ether (12 ml) was added to the reaction mixture and the precipitate was collected by filtration to give the objective compound (1.35 g) as a white powder.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US06348474B1 |
| 出典データセット | uspto-grants-2002_02 |
| ORD ID | ord-718f49d5480a4cad83c18676719d7df2 |
| 出典メモ | uspto-grants-2002_02 |