HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1011145Generated: October 31, 2026
Potassium Carbonate → HCID 57699599, compound
https://huagongshe.com/reaction/1011145
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1050496-83-7 | HCID 57699712 | — |
| Reactant | HCID 178448284 | HCID 178448284 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 57699599 | HCID 57699599 | 85.8% |
Reaction Steps
2-{[(1R)-1-Methylbutyl]oxy}-8-(methyloxy)-1H-purin-6-amine trifluoroacetate (100 mg, 0.274 mmol) was heated with potassium carbonate (37.8 mg, 0.274 mmol) in dry DMF (2 ml) at 60° C. under nitrogen for 1 hour and then cooled to room temperature. 4-(2-Bromoethyl)-2,2-dimethyltetrahydro-2H-pyran (72.6 mg, 0.328 mmol) was added and the reaction mixture heated at 50° C., for 16 hours. LCMS indicated the reaction to be incomplete and more 4-(2-bromoethyl)-2,2-dimethyltetrahydro-2H-pyran (35 mg) was added, and the reaction stirred at 50° C. for a further 5 hours and then partitioned between water (2 ml) and DCM (5 ml). The aqueous layer was further extracted with DCM (2×5 ml). The combined organic layers were combined and dried by passing through a hydrophobic frit and then evaporated to dryness using a nitrogen blowdown unit. The residue was dissolved in methanol (0.6 ml) and purified by mass directed autopreparation. Evaporation of the product containing fractions under a stream of nitrogen in a blowdown apparatus gave the title compound as a white solid (92 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07977344B2 |
|---|
| Source dataset | uspto-grants-2011_07 |
|---|
| ORD ID | ord-24538bed7f8f46ac84fed2321516cafc |
|---|
| Source note | uspto-grants-2011_07 |
|---|