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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 630557Erstellt: 25. Oktober 2026

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

https://huagongshe.com/reaction/630557

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAlendronic AcidHCID 2088—
EduktSodium HydroxideHCID 14798—
Edukt2-Nitrobenzenesulfonyl chlorideHCID 15540—
EduktSodiumHCID 5360545—
EduktAlendronate sodium anhydrousHCID 16760285—
LösungsmittelWaterHCID 962—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktSodium (4-(4-aminobenzenesulfonylamino)-1-hydroxybutane-1,1-diyl)bisphosphonateHCID 86725127—

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09315683B2
Quelldatensatzuspto-grants-2016_04
ORD IDord-1159bc41e38a46ff925c9b59b7e0d7c9
Quellennotizuspto-grants-2016_04