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HRID 630557作成日:2026年10月27日

Alendronic Acid → Sodium (4-(4-aminobenzenesulfonylamino)-1-hydroxybutane-1,1-diyl)bisphosphonate

https://huagongshe.com/reaction/630557

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Sodium HydroxideHCID 14798—
反応物2-Nitrobenzenesulfonyl chlorideHCID 15540—
反応物SodiumHCID 5360545—
反応物Alendronate sodium anhydrousHCID 16760285—
溶媒WaterHCID 962—
溶媒TetrahydrofuranHCID 8028—
生成物Sodium (4-(4-aminobenzenesulfonylamino)-1-hydroxybutane-1,1-diyl)bisphosphonateHCID 86725127—

反応手順

Sodium (4-(4-aminobenzenesulfonylamino)-1-hydroxybutane-1,1-diyl)bisphosphonate was synthesized using sodium alendronate. On this occasion, as the sodium alendronate, monosodium salt of (4-amino-1-hydroxybutane-1,1-diyl)bisphosphonic acid (manufactured by Zentiva) was used. An alendronate (34 g: 104 mmol) was added to 150 mL of pure water in a 500-mL beaker and was dissolved by adjusting the pH to 11 with an aqueous concentrated sodium hydroxide solution. To this solution was dropwise added nitrophenyl sulfonyl chloride (25 g: 110 mmol) dissolved in 100 mL of tetrahydrofuran. On this occasion, an aqueous sodium hydroxide solution was further added thereto to maintain the pH of the solution to 10 to 11. After completion of adding, this solution was stirred at room temperature for 2 hours. Subsequently, tetrahydrofuran was evaporated in vacuum, and the solution was adjusted to a pH of 4 to precipitate a solid, followed by cooling at 4 degrees Celsius overnight. Subsequently, the solid was collected by filtration and was washed with pure water and then dried to yield sodium (4-(4-aminobenzenesulfonylamino)-1-hydroxybutane-1,1-diyl)bisphosphonate.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09315683B2
出典データセットuspto-grants-2016_04
ORD IDord-1159bc41e38a46ff925c9b59b7e0d7c9
出典メモuspto-grants-2016_04