HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1010932Generated: October 26, 2026
Potassium Carbonate → 2-Butoxy-8-methoxy-9-(tetrahydrofuran-3-ylmethyl)-9H-purin-6-amine
https://huagongshe.com/reaction/1010932
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 3-(Bromomethyl)oxolane | HCID 14173422 | — |
| Reactant | HCID 178450370 | HCID 178450370 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-Butoxy-8-methoxy-9-(tetrahydrofuran-3-ylmethyl)-9H-purin-6-amine | HCID 57699603 | 53% |
Reaction Steps
2-Butoxy-8-methoxy-9H-purin-6-amine trifluoroacetate salt (0.20 g) was dissolved in anhydrous N,N-dimethylformamide (5 mL) was treated with anhydrous potassium carbonate (0.315 g), heated to 60° C. for 1 hour and then cooled to room temperature. To the above was added 3-(bromomethyl)tetrahydrofuran (0.103 g) and the reaction mixture heated at 50° C., overnight. The reaction mixture was quenched with water (25 mL) and extracted into ethyl acetate (3 times, 100 mL combined total volume). The combined organic phase was separated and passed through a hydrophobic frit to dry. The organic phase was stripped to give a gum which was purified by C18 reverse phase chromatography using water (containing 0.1% formic acid)-acetonitrile (containing 0.05% formic acid) as eluant (20-60%) to afford the title compound as a white solid (97 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07977344B2 |
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| Source dataset | uspto-grants-2011_07 |
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| ORD ID | ord-d9a3d438a04642ec8fdf822a6e281a42 |
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| Source note | uspto-grants-2011_07 |
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