HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 457696Generated: October 30, 2026
2-(Tributylstannyl)furan → HCID 10172251, compound
https://huagongshe.com/reaction/457696
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-(Tributylstannyl)furan | HCID 4393688 | — |
| Reactant | HCID 10309103 | HCID 10309103 | — |
| Catalyst | HCID 178418476 | HCID 178418476 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 10172251 | HCID 10172251 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07189730B2 |
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| Source dataset | uspto-grants-2007_03 |
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| ORD ID | ord-d004288931d3438b8952a8a2615d315f |
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| Source note | uspto-grants-2007_03 |
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