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HRID 547255作成日:2026年10月25日

2-Fluorothiophenol → HCID 10434433、化合物

https://huagongshe.com/reaction/547255

反応式

関与物質

役割名称HCID仕込み量
反応物2-FluorothiophenolHCID 520216—
反応物2-{6-[((1R,2R)-2-hydroxycyclopentyl)amino]-purin-9-yl}(4S,5S,3R)-5-(chloromethyl)oxolane-3,4-diolHCID 67189486—
溶媒DimethylformamideHCID 6228—
溶媒Sodium HydroxideHCID 14798—
生成物HCID 10434433HCID 1043443385.4%

反応手順

To a solution of 2-fluorothiophenol (38 mL, 406 mmol) in 2N sodium hydroxide (100 mL) was added 2-{6-[((1R,2R)-2-hydroxycyclopentyl)amino]purin-9-yl}(4S,5S,3R)-5-(chloromethyl)oxolane-3,4-diol (15.0 g, 40.6 mmol) in N,N-dimethylformamide (120 mL). The mixture was warmed to 100 C for 4 hours, following the progress of the reaction by TLC. The N,N-dimethylformamide was removed under reduced pressure, and the remaining mixture was diluted with water (200 mL), neutralized with acetic acid, extracted with ethyl acetate (3×125 mL), and the combined organic layers were dried over MgSO4. After removing the solvent under reduced pressure the residue was triturated with diethyl ether and filtered, to afford 16 grams of 2-{6-[((1R,2R)-2-hydroxycyclopentyl)amino]purin-9-yl}(4S,5S,3R)-5-[(2-fluorophenylthio)methyl]oxolane-3,4-diol as a white powder.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07939509B2
出典データセットuspto-grants-2011_05
ORD IDord-4d3b175681e0492eac47b52da4c361c7
出典メモuspto-grants-2011_05