HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1010989Generated: October 29, 2026
Potassium Carbonate → N2-Butyl-9-[(2,2-dimethyltetrahydro-2H-pyran-4-yl)methyl]-8-methoxy-9H-purine-2,6-diamine
https://huagongshe.com/reaction/1010989
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Lithium Bromide | HCID 82050 | — |
| Reactant | (2,2-Dimethyltetrahydro-2H-pyran-4-yl)methyl methanesulfonate | HCID 57699693 | — |
| Reactant | HCID 178448879 | HCID 178448879 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | N2-Butyl-9-[(2,2-dimethyltetrahydro-2H-pyran-4-yl)methyl]-8-methoxy-9H-purine-2,6-diamine | HCID 57699692 | 36.2% |
Reaction Steps
A mixture of N2-Butyl-8-methoxy-9H-purine-2,6-diamine trifluoroacetic acid salt (200 mg) and potassium carbonate (236 mg) in dry DMF (2 mL) were heated at 60° C. under nitrogen with stirring for 1 h. (2,2-Dimethyltetrahydro-2H-pyran-4-yl)methyl methanesulfonate (152 mg) was added and stirring was continued for 5 h at 50° C. The reaction was cooled to room temperature and stirred for 16 h. Lithium bromide (50 mg) was added and heating was continued for 5 h at 50° C., then 8 h at 90° 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 crude material (210 mg). This was purified by C18 reverse phase chromatography (ISCO) using water (0.1% formic acid)-acetonitrile (0.05% formic acid) as eluent (20-60%) to give the title compound (75 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-65944a1b126141288cea51ab8e8f8cb4 |
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| Source note | uspto-grants-2011_07 |
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