HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1011079Generated: October 31, 2026
Potassium Carbonate → N2-Butyl-8-(methyloxy)-9-[2-[(3R)-tetrahydro-3-furanyl]ethyl}-9H-Purine-2,6-diamine
https://huagongshe.com/reaction/1011079
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | (3S)-3-(2-bromoethyl)oxolane | HCID 52324314 | — |
| Reactant | HCID 178448876 | HCID 178448876 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | N2-Butyl-8-(methyloxy)-9-[2-[(3R)-tetrahydro-3-furanyl]ethyl}-9H-Purine-2,6-diamine | HCID 57699833 | 79.6% |
Reaction Steps
N2-Butyl-8-(methyloxy)-3H-purine-2,6-diamine (157 mg, 0.447 mmol) was heated in dry DMF (3 ml) with potassium carbonate (232 mg, 1.675 mmol) at 60° C. for one hour. (3S)-3-(2-Bromoethyl)tetrahydrofuran (100 mg, 0.558 mmol) in dry DMF (2 ml) was added and the mixture stirred and heated to 60° C. under nitrogen for 4 hours. The mixture was cooled to room temperature, quenched into water (40 ml) and extracted with ethyl acetate (3×25 ml). The organic extracts were combined, dried by passage through a hydrophobic frit and concentrated under vacuum. The residue was dissolved in 1:1 MeOH:DMSO and purified by mass directed autopreparation. The desired fractions were combined and concentrated using a nitrogen blowdown unit to give the title compound as a white solid (119 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-50c59ce09a894f1e973595b425e41c72 |
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| Source note | uspto-grants-2011_07 |
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