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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2354840Generated: October 31, 2026

4-Toluenesulfonyl chloride → HCID 23079461, compound

https://huagongshe.com/reaction/2354840

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Toluenesulfonyl chlorideHCID 7397—
ReactantTriethylamineHCID 8471—
ReactantSodium CyanideHCID 8929—
ReactantHCID 23079468HCID 23079468—
SolventPyridineHCID 1049—
SolventDimethylformamideHCID 6228—
ProductHCID 23079461HCID 2307946144.4%

Reaction Steps

2-Butoxy-9-(3-hydroxymethylbenzyl)adenine (0.09 g, 0.27 mmol), triethylamine (0.20 g, 1.98 mmol), tosyl chloride (0.30 g, 1.57 mmol) and pyridine (0.4 ml) were added to DMF (10 ml), and the mixture was stirred at room temperature for 24 hours. To the reaction mixture was added sodium cyanide (0.40 g, 9.16 mmol), and the mixture was stirred at 80° C. for 18 hours. After removing the solvent, the residue was poured into water and extracted with dichloromethane. The organic layer was dried over anhydrous magnesium sulfate, concentrated and the residue was purified by column chromatography (SiO2 20 g, eluting solvent: CHCl3/MeOH=100/1) to give 2-butoxy-9-(3-cyanomethylbenzyl)adenine (0.04 g, 0.12 mmol, yield: 44%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07754728B2
Source datasetuspto-grants-2010_07
ORD IDord-0bdfab0a7988489aba5a38ed5e4062b4
Source noteuspto-grants-2010_07