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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1616261Generated: October 30, 2026

Potassium Carbonate → 2-(Butyloxy)-9-(4-chlorobutyl)-8-(methyloxy)-9H-purin-6-amine

https://huagongshe.com/reaction/1616261

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant1-Bromo-4-chlorobutaneHCID 81364—
ReactantHCID 178450370HCID 178450370—
SolventDimethylformamideHCID 6228—
Product2-(Butyloxy)-9-(4-chlorobutyl)-8-(methyloxy)-9H-purin-6-amineHCID 5925261575.1%

Reaction Conditions

Temperature50 °C

Reaction Steps

2-(Butyloxy)-8-(methyloxy)-9H-purin-6-amine trifluoroacetate (2 g, 5.69 mmol) and potassium carbonate (1.967 g, 14.23 mmol) were suspended in DMF (20 ml) and heated to 50° C., under nitrogen for 30 mins. The mixture was cooled to room temperature, 1-bromo-4-chlorobutane (0.656 ml, 5.69 mmol) was added and stirring continued at room temperature for 20 hours. The solvent was evaporated under reduced pressure and the residue was partitioned between DCM (40 ml) and water (40 ml). The layers were separated using a hydrophobic frit and the aqueous layer washed with DCM (10 ml). The combined organic extracts were concentrated in vacuo to give crude material that was purified by silica chromatography using the FlashMaster (70 g cartridge) eluting with a cyclohexane:ethyl acetate 0-100% gradient over 30 mins. The product-containing fractions were combined and evaporated to give the title compound as a white solid (1.4 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08765772B2
Source datasetuspto-grants-2014_07
ORD IDord-3abc86cc7d374a2591ecbebc18182b22
Source noteuspto-grants-2014_07