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HRID 1665826Erstellt: 25. Oktober 2026

5'-O-(4,4'-Dimethoxytrityl)-2'-O-[2-(N-methylcarbamoyl)ethyl]-4-N-acetylcytidine → HCID 178485724, Verbindung

https://huagongshe.com/reaction/1665826

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt5'-O-(4,4'-Dimethoxytrityl)-2'-O-[2-(N-methylcarbamoyl)ethyl]-4-N-acetylcytidineHCID 53253292—
Edukt2-cyanoethoxy N,N,N',N'-tetraisopropylphosphorodiamiditeHCID 86638306—
EduktHCID 178458033HCID 178458033—
LösungsmittelAcetonitrileHCID 6342—
ProduktHCID 178485724HCID 17848572463%

Reaktionsschritte

The compound (480 mg, 0.71 mmol) prepared in Example 24 was dissolved in dried acetonitrile (2 mL). To the solution was added 2-cyanoethoxy N,N,N′,N′-tetraisopropylphosphorodiamidite (343 μL, 1.07 mmol) dissolved in dried acetonitrile (2 mL) and then diisopropylammonium 1H-tetrazolide (92 mg, 0.54 mmol), followed by vigorous stirring at room temperature for 15 hours. The reaction was terminated with a small amount of water, and then the reaction system was concentrated under reduced pressure, diluted with chloroform, and washed with saturated brine. The organic layer was dried with anhydrous sodium sulfate, and filtrate was concentrated under reduced pressure. The residue was subjected to silica gel column chromatography eluting with chloroform:methanol:triethylamine (98:1.5:0.5) to give the title compound (300 mg, 0.34 mmol).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08039611B2
Quelldatensatzuspto-grants-2011_10
ORD IDord-daea591bed8c44648f844e41ec12ab51
Quellennotizuspto-grants-2011_10