関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Ammonium Acetate | HCID 517165 | — |
| 反応物 | HCID 86604585 | HCID 86604585 | — |
| 溶媒 | Ethanol | HCID 702 | — |
| 生成物 | [2-(6-Chloro-pyridin-3-yl)-5-methyl-oxazol-4-yl]-acetic acid methyl ester | HCID 58765666 | 28.2% |
反応手順
A mixture of 6-chloro-nicotinic acid 3-methoxycarbonyl-1-methyl-2-oxo-propyl ester (16.3 g, 57.1 mmol) and ammonium acetate (18.5 g, 240 mmol) in ethanol (150 mL) is heated at 80° C. for 2 h, concentrated. The residue is taken into acetic acid (330 mL) and heated to reflux overnight, concentrated. The residue is taken into ethyl acetate and washed with water, dried, concentrated, purified by column giving [2-(6-Chloro-pyridin-3-yl)-5-methyl-oxazol-4-yl]-acetic acid methyl ester (4.3 g).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07259175B2 |
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| 出典データセット | uspto-grants-2007_08 |
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| ORD ID | ord-5f10ed2fc9794b8e88d73155e565eba6 |
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| 出典メモ | uspto-grants-2007_08 |
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