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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 457696Generated: October 30, 2026

2-(Tributylstannyl)furan → HCID 10172251, compound

https://huagongshe.com/reaction/457696

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(Tributylstannyl)furanHCID 4393688—
ReactantHCID 10309103HCID 10309103—
CatalystHCID 178418476HCID 178418476—
SolventTetrahydrofuranHCID 8028—
ProductHCID 10172251HCID 10172251—

Reaction Conditions

Temperature60 °C

Reaction Steps

A mixture of 2-(2-phenylethylamino)-8-bromo-9-ethyl-9H-purin-6-ylamine (0.28 mmol), tributylstannyl furan (440 μL, 1.4 mmol), and bis(triphenylphosphine)palladium dichloride (12 mg, 0.017 mmol) was dissolved in dry tetrahydrofuran (10 mL), and heated at 60° C. for 3 hours. The solvent was removed in vacuo, and the residue was partitioned between water and chloroform. The organic layer was dried (Na2SO4), filtered and concentrated in vacuo. The residue was dissolved in CHCl3/MeOH and extracted with chloroform. The organic layers were dried over Na2SO4 and concentrated in vacuo. The residue was chromatographed on a silica gel column eluting with ethyl acetate/cyclohexane/methanol (60/36/4) to give 2-(2-phenylethylamino)-8-(furan-2-yl)-9-ethyl-9H-purin-6-ylamine as a chromatographically pure solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07189730B2
Source datasetuspto-grants-2007_03
ORD IDord-d004288931d3438b8952a8a2615d315f
Source noteuspto-grants-2007_03