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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1684975Generated: November 2, 2026

4-Toluenesulfonyl chloride → HCID 23079461, compound

https://huagongshe.com/reaction/1684975

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 numberUS08148371B2
Source datasetuspto-grants-2012_04
ORD IDord-b8e701a33239417f9fefa8b6ae4ac84e
Source noteuspto-grants-2012_04