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HRID 535209作成日:2026年10月26日

Alendronic Acid → 4-Aminobenzamide

https://huagongshe.com/reaction/535209

反応式

関与物質

役割名称HCID仕込み量
反応物Alendronic AcidHCID 2088—
反応物2-Nitrobenzoyl chlorideHCID 11875—
反応物Sodium HydroxideHCID 14798—
反応物Alendronate sodium anhydrousHCID 16760285—
溶媒WaterHCID 962—
溶媒TetrahydrofuranHCID 8028—
生成物4-AminobenzamideHCID 76079—
生成物Alendronate sodium anhydrousHCID 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

DOI10.6084/m9.figshare.5104873.v1
特許番号US08858695B2
出典データセットuspto-grants-2014_10
ORD IDord-c85c51da5815432c804935d31ca0b10f
出典メモuspto-grants-2014_10