関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | 2,4,6-Trimethylpyridine | HCID 7953 | — |
| 反応物 | Phenyl chloroformate | HCID 15891 | — |
| 反応物 | 6-Bromoimidazo[1,2-a]pyridin-2-amine | HCID 44119296 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | (6-Bromo-imidazo[1,2-a]pyridin-2-yl)-carbamic acid phenyl ester | HCID 59251768 | — |
反応手順
To a solution of 6-bromo-imidazo[1,2-a]pyridin-2-ylamine (Intermediate A1)(6.2 g, 29.2 mmol) in THF (400 ml) is added 2,4,6-trimethylpyridine (5.8 ml, 43.9 mmol). The reaction mixture is cooled to 0° C. (ice-bath) and treated dropwise with a solution of phenyl chloroformate (3.85 ml, 30.7 mmol) in THF (50 ml) over 15 minutes. The reaction mixture is stirred overnight, at room temperature, quenched with water and stirred for a further 5 minutes resulting in a white precipitate. The solid is collected by filtration and dried under vacuum (40° C.) overnight to afford the title compound [MH+ 331.99 and 333.99].
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08053574B2 |
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| 出典データセット | uspto-grants-2011_11 |
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| ORD ID | ord-d2967969602f4d4daaba04f8a599af03 |
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| 出典メモ | uspto-grants-2011_11 |
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