Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Isobutylamine | HCID 6558 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 69827476 | HCID 69827476 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | HCID 69827510 | HCID 69827510 | — |
Reaction Steps
To a solution of 9-{(3aR,4R,6S,6aR)-6-[3-(tert-butyl)-1,2,4-oxadiazol-5-yl]-2,2-dimethyltetrahydrofuro[3,4-d][1,3]dioxol-4-yl}-6-(1H-1,2,3-benzotriazol-1-yloxy)9H-purine (50 mg) in dimethylsulfoxide (0.4 ml) was added diisopropylethylamine (0.1 ml) and isobutylamine (0.038 ml). The mixture was stirred at 20° C. for 16 h under nitrogen. The mixture was then evaporated to dryness in vacuo to give a residue that was purified by automated preparative HPLC to afford the title compound (14 mg) as a white compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06492348B1 |
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| Source dataset | uspto-grants-2002_12 |
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| ORD ID | ord-5fb0c90f139a40f88e304f02fa63a2de |
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| Source note | uspto-grants-2002_12 |
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