関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Alendronic Acid | HCID 2088 | — |
| 反応物 | 2-Nitrobenzoyl chloride | HCID 11875 | — |
| 反応物 | Sodium Hydroxide | HCID 14798 | — |
| 反応物 | Alendronate sodium anhydrous | HCID 16760285 | — |
| 溶媒 | Water | HCID 962 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | 4-Aminobenzamide | HCID 76079 | — |
| 生成物 | Alendronate sodium anhydrous | HCID 16760285 | — |
反応手順
The 4-aminobenzamide of alendronate sodium was prepared as follows. In a 500 mL beaker, 54 g (166 mmol) of sodium alendronate was dissolved in 150 mL of DI water with a pH adjusted to 11 with concentrated NaOH. Nitrobenzoyl chloride, 28 g (150 mmol), dissolved in 100 mL of THF, was added dropwise into the aqueous alendronate solution. The pH was kept at 11 with additional NaOH solution during the addition. After the addition was complete, the solution was stirred for another 2 hours at room temperature. THF was removed in vacuo, and the pH of the solution was adjusted to 4. The resulting precipitate, which was collected by filtration at room temperature, was primarily nitrobenzoic acid and was discarded. The solution was kept at 4° C. overnight, and the resulting precipitate was collected by filtration, washed with DI water, and dried. The resulting solid weighted approximately 56 g (86%).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08858695B2 |
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| 出典データセット | uspto-grants-2014_10 |
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| ORD ID | ord-c85c51da5815432c804935d31ca0b10f |
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| 出典メモ | uspto-grants-2014_10 |
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