Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1953069Generated: October 27, 2026

Trimethylsilylacetylene → 2',3'-bis-O-(tert-butyldimethylsilyl)-5'-deoxy-5-[(trimethylsilyl)ethynyl]-N4-(n-pentyloxycarbonyl)-cytidine

https://huagongshe.com/reaction/1953069

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethylsilylacetyleneHCID 66111—
Reactant2',3'-Bis-o-(tert-butyldimethylsilyl)-5'-deoxy-5-iodo-n4-(n-pentyloxycarbonyl)cytidineHCID 53922475—
CatalystHCID 178418476HCID 178418476—
SolventDichloromethaneHCID 6344—
SolventTriethylamineHCID 8471—
Product2',3'-bis-O-(tert-butyldimethylsilyl)-5'-deoxy-5-[(trimethylsilyl)ethynyl]-N4-(n-pentyloxycarbonyl)-cytidineHCID 6880075026%

Reaction Steps

To a solution of 2',3'-bis-O-(tert-butyldimethylsilyl)-5'-deoxy-5-iodo-N4 -(n-pentyloxycarbonyl)cytidine (130 mg, 0.18 mmol) in CH2Cl2 (2 ml) and Et3N(2 ml) Cul (10.7 mg, 0.1056 mmol), Pd(PPh3)2Cl2 (2.6 mg, 0.0036 mmol), and trimethylsilyl-acetylene (58.6 μl, 0.40 mmol) were added and stirred for 2 hours at room temperature under Ar in the dark. The reaction mixture was concentrated under reduced pressure and the residue was dissolved in EtOAc(25 ml×3), washed with 2% aq. EDTA.2Na(10 ml×2), water and brine, dried over Na2SO4 and filtered. The filtrate was evaporated under reduced pressure. The crude product was purified by flash chromatography on SiO2 (eluent: 10% EtOAc/n-hexane) to give 2',3'-bis-O-(tert-butyidimethylsilyl)-5'-deoxy-5-[(trimethylsilyl)ethynyl]-N4 -(n-pentyloxycarbonyl)-cytidine as a colorless amorphous solid. (30.2 mg, 26% yield)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06114520
Source datasetuspto-grants-2000_09
ORD IDord-65c9315d1acc4516b1defe96ba060532
Source noteuspto-grants-2000_09