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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 630557생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/630557

반응식

참여 물질

역할이름HCID투입량
반응물Alendronic AcidHCID 2088—
반응물Sodium HydroxideHCID 14798—
반응물2-Nitrobenzenesulfonyl chlorideHCID 15540—
반응물SodiumHCID 5360545—
반응물Alendronate sodium anhydrousHCID 16760285—
용매WaterHCID 962—
용매TetrahydrofuranHCID 8028—
생성물Sodium (4-(4-aminobenzenesulfonylamino)-1-hydroxybutane-1,1-diyl)bisphosphonateHCID 86725127—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09315683B2
출처 데이터셋uspto-grants-2016_04
ORD IDord-1159bc41e38a46ff925c9b59b7e0d7c9
출처 메모uspto-grants-2016_04