関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | 2,6-Diaminopyridine | HCID 8861 | — |
| 反応物 | (2-Methoxyethoxy)acetic acid | HCID 27642 | — |
| 反応物 | Isobutyl chloroformate | HCID 62365 | — |
| 反応物 | Sodium Bicarbonate | HCID 516892 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 溶媒 | Triethylamine | HCID 8471 | — |
| 生成物 | N-(6-Amino-pyridin-2-yl)-2-(2-methoxy-ethoxy)-acetamide | HCID 57600508 | — |
反応手順
4.9 ml of (2-methoxyethoxy)-acetic acid is dissolved in 500 ml of tetrahydrofuran. 9.7 ml of triethylamine and 5.6 ml of isobutyl chloroformate are added at 0° C., and it is stirred for 30 minutes at 0° C. 3.96 g of 2,6-diaminopyridine is added, and it is stirred for another 4 hours at room temperature. The reaction mixture is mixed with semi-saturated sodium bicarbonate solution and extracted with ethyl acetate. The organic solution is washed with saturated sodium chloride solution, dried on sodium sulfate, concentrated by evaporation, and after purification by chromatography on silica gel, 5.04 g of the title compound is obtained.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07511059B2 |
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| 出典データセット | uspto-grants-2009_03 |
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| ORD ID | ord-1dda6433de5b4aab9845db9fde330951 |
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| 出典メモ | uspto-grants-2009_03 |
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