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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1010938Generated: October 30, 2026

Water → N2-Butyl-8-methoxy-9-[2-(tetrahydrofuran-2-yl)ethyl]-9H-Purine-2,6-diamine

https://huagongshe.com/reaction/1010938

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium CarbonateHCID 11430—
Reactant2-(2-Bromoethyl)oxolaneHCID 53691871—
ReactantHCID 178448879HCID 178448879—
SolventDimethylformamideHCID 6228—
ProductN2-Butyl-8-methoxy-9-[2-(tetrahydrofuran-2-yl)ethyl]-9H-Purine-2,6-diamineHCID 57699707—

Reaction Conditions

Temperature60 °C

Reaction Steps

A stirring mixture of N2-butyl-8-methoxy-9H-purine-2,6-diamine trifluoroacetic acid salt (200 mg) and potassium carbonate (236 mg) in dry N,N-dimethylformamide (2 ml) was heated with stirring at 60° C. for 1 h. 2-(2-Bromoethyl)tetrahydrofuran (122 mg) was added and the stirring mixture heated at 50° C. for 4 h. After allowing to cool, water was added and the mixture extracted three times with ethyl acetate. The combined extracts were washed with water then brine, dried by passing through a phase separation cartridge and stripped to give a brown oil. This was purified by C18 reverse phase chromatography using water (containing 0.1% formic acid)-acetonitrile (containing 0.05% formic acid) as eluent (20-60%) and the appropriate fractions combined and evaporated to remove acetonitrile. The remaining aqueous mixture was made basic with saturated sodium hydrogen carbonate, extracted three times with dichloromethane and the combined extracts dried by passing through a phase separation cartridge then evaporated to afford the title compound, yield 107 mg.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07977344B2
Source datasetuspto-grants-2011_07
ORD IDord-e8170ffc71b04f94a7fb086f575bd606
Source noteuspto-grants-2011_07