化工社化工社 化学情報印刷レポート · 研究参考用
Water → Methyl 5-(3-methyl-1,2,4-oxadiazol-5-yl)-3-pyridinecarboxylate
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Water | HCID 962 | — |
| 反応物 | Ethyl Acetate | HCID 8857 | — |
| 反応物 | Thionyl Chloride | HCID 24386 | — |
| 反応物 | 5-(3-Methyl-1,2,4-oxadiazol-5-yl)-3-pyridinecarboxylic acid | HCID 18945441 | — |
| 溶媒 | Methanol | HCID 887 | — |
| 生成物 | Methyl 5-(3-methyl-1,2,4-oxadiazol-5-yl)-3-pyridinecarboxylate | HCID 18945172 | — |
反応手順
Thionyl chloride (2.5 ml) was added dropwise in methanol (25 ml) under cooling at 7°-9° C. After the mixture was stirred for 30 minutes at the same temperature, 5-(3-methyl-1,2,4-oxadiazol-5-yl)-3-pyridinecarboxylic acid (2.5 g) was added thereto and the mixture was refluxed for 3 hours. After being cooled to room temperature, the mixture was poured into a mixture of ethyl acetate (100 ml) and water (100 ml). The organic layer was successively washed with 10% potassium carbonate aqueous solution and brine, and then dried over magnesium sulfate. The solvent was evaporated in vacuo and the residue was recrystallized from diethyl ether to afford methyl 5-(3-methyl-1,2,4-oxadiazol-5-yl)-3-pyridinecarboxylate (2.12 g).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05824691 |
| 出典データセット | uspto-grants-1998_10 |
| ORD ID | ord-c530c3da336340a2a690ddab9eb9c047 |
| 出典メモ | uspto-grants-1998_10 |