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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 630557Generated: October 25, 2026

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

https://huagongshe.com/reaction/630557

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAlendronic AcidHCID 2088—
ReactantSodium HydroxideHCID 14798—
Reactant2-Nitrobenzenesulfonyl chlorideHCID 15540—
ReactantSodiumHCID 5360545—
ReactantAlendronate sodium anhydrousHCID 16760285—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductSodium (4-(4-aminobenzenesulfonylamino)-1-hydroxybutane-1,1-diyl)bisphosphonateHCID 86725127—

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09315683B2
Source datasetuspto-grants-2016_04
ORD IDord-1159bc41e38a46ff925c9b59b7e0d7c9
Source noteuspto-grants-2016_04