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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1666201Generated: October 26, 2026

Potassium Carbonate → 9-(1-tert-Butoxycarbonylpiperidin-4-ylethyl)-8-methoxy-2-(2-methoxyethoxy)adenine

https://huagongshe.com/reaction/1666201

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactanttert-Butyl 4-(2-((methanesulfonyl)oxy)ethyl)piperidine-1-carboxylateHCID 15229596—
Reactant8-Methoxy-2-(2-methoxyethoxy)-9H-purine-6-amineHCID 57699791—
SolventDimethylformamideHCID 6228—
Product9-(1-tert-Butoxycarbonylpiperidin-4-ylethyl)-8-methoxy-2-(2-methoxyethoxy)adenineHCID 5928802160%

Reaction Conditions

Temperature60 °C

Reaction Steps

8-Methoxy-2-(2-methoxyethoxy)adenine (3.27 g, 13.7 mmol) was dissolved in DMF (75 ml), and thereto were added potassium carbonate (1.89 g, 13.7 mmol) and 4-[2-(methanesulfonyloxy)ethyl]piperidine-1-carboxylic acid tert-butyl ester (4.21 g, 13.7 mmol), and the mixture was stirred at 60° C. for 2.5 hours. The mixture was cooled to room temperature, and the carbonate salt was removed by filtration, and the filtrate was concentrated. To the residue was added water, and the mixture was extracted three times with chloroform. The resultant was dried over magnesium sulfate, and concentrated. The residue was purified by silica gel column (chloroform/methanol=200/1 to 100/1) to give the subtitle compound (3.62 g, 8.04 mmol) as a white solid. Yield: 60%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08044056B2
Source datasetuspto-grants-2011_10
ORD IDord-49af5b3e7cbe4db5a206163a0bd009bd
Source noteuspto-grants-2011_10