関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Sodium Hydroxide | HCID 14798 | — |
| 反応物 | 2-Acetoxybenzoyl chloride | HCID 79668 | — |
| 反応物 | Alendronate Sodium | HCID 23681107 | — |
| 触媒 | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| 触媒 | Tetrahexylammonium iodide | HCID 75056 | — |
| 溶媒 | Water | HCID 962 | — |
| 溶媒 | Diethyl Ether | HCID 3283 | — |
| 生成物 | [4-(2-Acetoxybenzoyl)-amino-1-hydroxybutylidene]-diphosphonic acid | HCID 86749102 | — |
反応手順
3.18 g (9.8 mmoles ) of sodium trihydrogen 4-amino-1-hydroxybutylidenediphosphonate trihydrate are added in 30 ml of water to 1.8 g (45 mmoles) of sodium hydroxide, 100 mg of p-dimethylaminopyridine and 200 mg of tetrahexylammonium iodide. The resulting solution is cooled to 0° C., and added with 2.03 g (10.2 mmoles) of 2-acetoxybenzoic acid chloride dissolved in 10 ml of diethyl ether. The reaction mixture is stirred for 2 hours at room temperature, then it is extracted with ethyl ether and the aqueous solution is acidified with concentrated HCl under stirring, with cooling. [4-(2-Hydroxybenzoyl)-amino-1-hydroxybutylidene]-diphosphonic acid precipitates, which is filtered, washed and dried at 70° C. and transformed into the title product by means of acetylation with acetic anhydride.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US05466682 |
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| 出典データセット | uspto-grants-1995_11 |
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| ORD ID | ord-000990f6f7624768a2d521f93c51d0f7 |
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| 出典メモ | uspto-grants-1995_11 |
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