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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 983181Generated: October 31, 2026

HCID 10632308, compound → HCID 20716774, compound

https://huagongshe.com/reaction/983181

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 10632308HCID 10632308—
ReactantHCID 20716771HCID 20716771—
SolventAcetonitrileHCID 6342—
SolventEthyl AcetateHCID 8857—
ProductHCID 20716774HCID 2071677498%

Reaction Steps

To a solution of 2′-O-(5-aminopentyl)-5′-O-(4,4′-dimethoxytrityl)-adenosine (1.0 g, 1.52 mmol) in anhydrous CH3CN (8.0 mL) was added with stirring, under argon, N-(2-Cyanoethoxycarbonyl)oxy succinimide (0.43 g, 2.02 mmol) After stirring for 5 h at room temperature the reaction mixture was diluted with EtOAc (50 mL) and washed with aq saturated bicarbonate (3×20 mL) and water (20 mL), dried (Na2SO4) and evaporated to give 53 as a light yellow foam (1.1 g, 98% yield). This compound was used without further purification for the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06861514B2
Source datasetuspto-grants-2005_03
ORD IDord-e007eeea0fdc48698d69efc11c8b2b04
Source noteuspto-grants-2005_03