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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 552717생성일: 2026년 10월 27일

EDTA disodium salt → {(3aR,4R,6R,6aR)-6-[6-(4-Fluorobenzyl)-9H-purin-9-yl]-2,2-dimethyl-tetrahydrofuro[3,4-d][1,3]dioxol-4-yl}methyl acetate

https://huagongshe.com/reaction/552717

반응식

참여 물질

역할이름HCID투입량
반응물EDTA disodium saltHCID 8759—
반응물Ammonium ChlorideHCID 25517—
반응물((3aR,4R,6R,6aR)-6-(6-chloro-9H-purin-9-yl)-2,2-dimethyltetrahydrofuro[3,4-d][1,3]dioxol-4-yl)methyl acetateHCID 86607315—
반응물HCID 178505764HCID 178505764—
촉매HCID 178418397HCID 178418397—
용매TetrahydrofuranHCID 8028—
생성물{(3aR,4R,6R,6aR)-6-[6-(4-Fluorobenzyl)-9H-purin-9-yl]-2,2-dimethyl-tetrahydrofuro[3,4-d][1,3]dioxol-4-yl}methyl acetateHCID 6716429473%

반응 단계

[(3aR,4R,6R,6aR)-6-(6-Chloro-9H-purin-9-yl)-2,2-dimethyltetrahydrofuro[3,4-d][1,3]dioxol-4-yl]methyl acetate (369 mg, 0.00100 mol) and tetrakis(triphenylphosphine)palladium(0) (58 mg, 0.000050 mol) were dissolved in tetrahydrofuran (10 mL) at room temperature under nitrogen. 0.5 M of 4-fluorobenzylzinc chloride in tetrahydrofuran (3 mL) was added dropwise over 10 min. The solution was stirred under nitrogen at room temperature for 15 min then heated at 60° C. for 3 h. The reaction was allowed to cool to r.t then poured on saturated NH4Cl (10 mL). Saturated Na2EDTA (10 mL) was added and the solution extracted three times with EtOAc. The organics were pooled and extracted twice with saturated Na2EDTA then once with brine, dried over Na2SO4 and concentrated in vacuo. The residue was purified by flash chromatography (DCM/EtOAc 10% to 50%) to obtain the product (322 mg, 73%) as an oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07951810B2
출처 데이터셋uspto-grants-2011_05
ORD IDord-602aae8bd26141b699a258d8e039412d
출처 메모uspto-grants-2011_05