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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1011053Generated: October 25, 2026

Potassium Carbonate → N2-Butyl-8-(methoxy)-9-(tetrahydro-3-furanylmethyl)-9H-Purine-2,6-diamine

https://huagongshe.com/reaction/1011053

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant(Tetrahydrofuran-3-yl)methyl methanesulfonateHCID 22273010—
Reactant2,6-Dichloro-9-(tetrahydro-2H-pyran-4-ylmethyl)-9H-purineHCID 57699703—
ReactantHCID 178448879HCID 178448879—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductN2-Butyl-8-(methoxy)-9-(tetrahydro-3-furanylmethyl)-9H-Purine-2,6-diamineHCID 57699650—

Reaction Conditions

Temperature60 °C

Reaction Steps

To a solution of N2-butyl-8-methoxy-9H-purine-2,6-diamine trifluoroacetic acid salt (4.60 g) in dry N,N-dimethylformamide (55 ml) at room temperature and under was added potassium carbonate (7.25 g) in one go. The reaction was heated to 60° C. for 1.5 hours. A solution of tetrahydro-3-furanylmethyl methanesulfonate, Isomer 2 (2.6 g) in dry N,N-dimethylformamide (3 ml) was added via a Pasteur pipette and the reaction heated at 70° C. for 16 hours. The reaction was cooled to room temperature, diluted with ethyl acetate (100 ml) and washed with brine (20 ml). The organic layer was concentrated in vacuo. The product was purified by C18 reverse phase chromatography using water (0.1% formic acid)-acetonitrile (0.05% formic acid) as eluant (10-60%) to afford the title compound as a clear viscous oil (3 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07977344B2
Source datasetuspto-grants-2011_07
ORD IDord-1a637a32dbec4729852269de4ac157ba
Source noteuspto-grants-2011_07