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4-Aminopyridine → 2-(4-Pyridyl)-hexahydroisoindole-1,3-dione
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 4-Aminopyridine | HCID 1727 | — |
| 反応物 | Methanesulfonic Acid | HCID 6395 | — |
| 反応物 | Hexahydrophthalic anhydride, cis- | HCID 641660 | — |
| 溶媒 | O-Xylene | HCID 7237 | — |
| 生成物 | 2-(4-Pyridyl)-hexahydroisoindole-1,3-dione | HCID 12822541 | — |
反応手順
The starting material is prepared as follows: The mixture of 23.5 g of 4- aminopyridine, 38.5 g of cis-1,2-cyclohexanedicarboxylic acid anhydride and 400 ml of xylene is refluxed for 42 hours while stirring and separating the water formed. After the first half-hour, and after 18 hours, 1 ml of methane sulfonic acid is added to the mixture. It is filtered hot, the crystals formed after cooling are filtered off and recrystallized from isopropanol, to yield the 2-(4-pyridyl)-hexahydroisoindole-1,3-dione melting at 165°-168°.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04255429 |
| 出典データセット | uspto-grants-1981_03 |
| ORD ID | ord-aa672faddfbb46fe8114bfc5b5f4b947 |
| 出典メモ | uspto-grants-1981_03 |