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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1488558Generated: November 1, 2026

Pyridine → HCID 178430607, compound

https://huagongshe.com/reaction/1488558

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantDiisopropylamineHCID 7912—
Reactant2-Cyanoethyl N,N-diisopropylchlorophosphoramiditeHCID 2734844—
ReactantHCID 67680270HCID 67680270—
SolventTetrahydrofuranHCID 8028—
ProductHCID 178430607HCID 17843060756%

Reaction Steps

79.7 mg (0.2 mmol) of 5'-[(2-naphthyl)methylthio]-5'-deoxythymidine [prepared as described in step (a) above] were dried by azeotropic distillation with pyridine and then dissolved in 2.5 ml of tetrahydrofuran. 0.084 ml (0.48 mmol) of diisopropylamine was then added to the solution. 54 μl (0.24 mmol) of 2-cyanoethyl N,N-diisopropylchlorophosphoramidite were then added dropwise to the mixture, under an atmosphere of argon. The resulting mixture was stirred at room temperature for 1.75 hours under the same atmosphere. The tetrahydrofuran was then removed by distillation under reduced pressure. The resulting residue was dissolved in 10 ml of 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 distilled off under reduced pressure, and the residue was purified by column chromatography through 10 g of silica gel (70-230 mesh), using ethyl acetate as the eluent, to give 67 mg (yield 56%) of the title compound as a foam-like substance.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05674856
Source datasetuspto-grants-1997_10
ORD IDord-d15ef826fc124f6eb8736dfd9be215f1
Source noteuspto-grants-1997_10