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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2393319Erstellt: 24. Oktober 2026

Pyridine → HCID 178457339, Verbindung

https://huagongshe.com/de/reaction/2393319

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPyridineHCID 1049—
Edukt2-Cyanoethyl tetraisopropylphosphorodiamiditeHCID 128153—
EduktN-[1-[(2R,4S,5R)-4-hydroxy-5-(trityloxymethyl)oxolan-2-yl]-2-oxopyrimidin-4-yl]benzamideHCID 494349—
EduktHCID 178458033HCID 178458033—
LösungsmittelDichloromethaneHCID 6344—
ProduktHCID 178457339HCID 17845733962%

Reaktionsschritte

402 mg (0.7 mmol) of 5'-O-trityl-N-benzoyl-2'-deoxycytidine [prepared as described in step (a) above] were dried by azeotropic distillation with pyridine and then dissolved in 3.5 ml of methylene chloride. 60 mg (0.35 mmol) of diisopropylammonium tetrazolide were added to the solution. 245 μl (0.77 mmol) of 2-cyanoethyl N,N,N',N'-tetraisopropylphosphorodiamidite were then added dropwise, under an atmosphere of argon. The resulting mixture was stirred at room temperature for 3.5 hours under same atmosphere. At the end of this time, the methylene chloride was removed by distillation under reduced pressure. The resulting residue was dissolved in ethyl acetate, and the solution was washed with a 10% w/v aqueous solution of sodium carbonate and with a saturated aqueous solution of sodium chloride, in that order. The solution was then dried over anhydrous magnesium sulfate, after which the solvent was removed by distillation under reduced pressure, and the residue was purified by column chromatography through 23 g of silica gel (70-230 mesh), using ethyl acetate as the eluent, to give 337 mg (yield 62%) of the title compound as a foam substance.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05807837
Quelldatensatzuspto-grants-1998_09
ORD IDord-76901d2b60214939b6366170be25f388
Quellennotizuspto-grants-1998_09