HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1010988Generated: October 31, 2026
Potassium Carbonate → 2-Butyloxy-9-[(2,2-dimethyltetrahydro-2H-pyran-4-yl)methyl]-8-methoxy-9H-purin-6-amine
https://huagongshe.com/reaction/1010988
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-(Bromomethyl)-2,2-dimethyloxane | HCID 57699699 | — |
| Reactant | HCID 178450370 | HCID 178450370 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-Butyloxy-9-[(2,2-dimethyltetrahydro-2H-pyran-4-yl)methyl]-8-methoxy-9H-purin-6-amine | HCID 57699605 | 78.4% |
Reaction Steps
A mixture of 2-butoxy-8-methoxy-9H-purin-6-amine trifluoroacetate salt (223 mg) and potassium carbonate (264 mg) in dry DMF (2 mL) were heated at 60° C. under nitrogen with stirring for 1 h. 4-(Bromomethyl)-2,2-dimethyltetrahydro-2H-pyran (158 mg) was added and the reaction was stirred for 16 h at 60° C. The mixture was quenched with water and extracted with EtOAc (×3). The combined organics were washed with water and brine, dried using a hydrophobic frit and evaporated to give a brown oil. The crude material was purified by normal phase chromatography (ISCO) using 5-20% methanol/EtOAc as eluent to give a pale oil (181 mg). The material was re-purified by normal phase chromatography (ISCO) using 0-15% methanol/EtOAc as eluent to give the title compound (161 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07977344B2 |
|---|
| Source dataset | uspto-grants-2011_07 |
|---|
| ORD ID | ord-4a464e7cbb2a41c8851e2348f8264382 |
|---|
| Source note | uspto-grants-2011_07 |
|---|