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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1165363Erstellt: 27. Oktober 2026

2-Cyanoethyl tetraisopropylphosphorodiamidite → N-biotinyl-aminoethyl 2-cyanoethyl N,N-diisopropylphosphoramidite

https://huagongshe.com/reaction/1165363

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2-Cyanoethyl tetraisopropylphosphorodiamiditeHCID 128153—
EduktSodium BicarbonateHCID 516892—
EduktN-biotinylaminoethanolHCID 131716339—
EduktHCID 178458033HCID 178458033—
LösungsmittelDimethylformamideHCID 6228—
ProduktN-biotinyl-aminoethyl 2-cyanoethyl N,N-diisopropylphosphoramiditeHCID 15085418—

Reaktionsschritte

To a solution of 150 mg of N-biotinylaminoethanol (2a) in 5 ml of dry DMF was added 65 mg of diisopropylammonium tetrazolide and 0.300 ml of 2-cyanoethyl N,N,N',N'-tetraisopropylphosphorodiamidite. The resulting solution was stirred at room temperature for 1.25 hr and then poured onto 50 ml of 5% aqueous sodium bicarbonate. The mixture was extracted with two 50 ml portions of methylene chloride, and the combined extracts were washed with 5% sodium bicarbonate and brine, dried over sodium sulfate, and evaporated to afford the crude product as a thick oil. This was dissolved in 2 ml of dry methylene chloride, affording a solution that was added dropwise to 30 ml of rapidly stirring petroleum ether. The colorless precipitate that formed was collected by suction filtration under argon, affording after drying at room temperature under vacuum 109 mg (43%) of a colorless solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04908453
Quelldatensatzuspto-grants-1990_03
ORD IDord-27e1cf4b3e724bb69da2d6e18c0549f7
Quellennotizuspto-grants-1990_03