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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1488551Generated: October 25, 2026

Pyridine → HCID 178457339, compound

https://huagongshe.com/reaction/1488551

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
Reactant2-Cyanoethyl tetraisopropylphosphorodiamiditeHCID 128153—
ReactantN-[1-[(2R,4S,5R)-4-hydroxy-5-(trityloxymethyl)oxolan-2-yl]-2-oxopyrimidin-4-yl]benzamideHCID 494349—
ReactantHCID 178458033HCID 178458033—
SolventDichloromethaneHCID 6344—
ProductHCID 178457339HCID 17845733962%

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05674856
Source datasetuspto-grants-1997_10
ORD IDord-94af2afc85164d09a65422ce81ed72d3
Source noteuspto-grants-1997_10