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HRID 1665823作成日:2026年10月27日

5'-O-(4,4'-Dimethoxytrityl)-2'-O-[2-(N-methylcarbamoyl)ethyl]uridine → HCID 178485725、化合物

https://huagongshe.com/reaction/1665823

反応式

関与物質

役割名称HCID仕込み量
反応物5'-O-(4,4'-Dimethoxytrityl)-2'-O-[2-(N-methylcarbamoyl)ethyl]uridineHCID 53253859—
反応物2-cyanoethoxy N,N,N',N'-tetraisopropylphosphorodiamiditeHCID 86638306—
反応物HCID 178458033HCID 178458033—
溶媒AcetonitrileHCID 6342—
生成物HCID 178485725HCID 17848572578%

反応手順

The compound (490 mg, 0.77 mmol) prepared in Example 8 was dissolved in dried acetonitrile (2 mL), and 2-cyanoethoxy N,N,N′,N′-tetraisopropylphosphorodiamidite (358 mg, 1.19 mmol) dissolved in dried acetonitrile (2 mL) was added thereto. To the mixture was further added diisopropylammonium 1H-tetrazolide (101 mg, 0.59 mmol), followed by stirring at room temperature for 8 hours. The reaction was terminated by adding water thereto, and dilution with ethyl acetate was carried out. The organic layer was washed with saturated brine three times and a saturated sodium hydrogen carbonate aqueous solution three times. The organic layer was dried with anhydrous sodium sulfate and filtered. The filtrate was concentrated under reduced pressure. The residue was subjected to silica gel column chromatography eluting with chloroform:methanol (99:1, v/v) containing 0.5% triethylamine to give the title compound (384 mg, 66%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08039611B2
出典データセットuspto-grants-2011_10
ORD IDord-4a1b9da55fb0403e8c1380fecb14414f
出典メモuspto-grants-2011_10