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HRID 552717作成日:2026年10月27日

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

反応式

関与物質

役割名称HCID仕込み量
反応物EDTA disodium saltHCID 8759—
反応物Ammonium ChlorideHCID 25517—
反応物((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—
反応物HCID 178505764HCID 178505764—
触媒HCID 178418397HCID 178418397—
溶媒TetrahydrofuranHCID 8028—
生成物{(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%

反応手順

[(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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07951810B2
出典データセットuspto-grants-2011_05
ORD IDord-602aae8bd26141b699a258d8e039412d
出典メモuspto-grants-2011_05