HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Nitropyridine N-oxide → 4-(4-amino-3-iodo-1H-pyrazolo[3,4-d]pyrimidin-1-yl)-1-pyridiniumolate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Nitropyridine N-oxide | HCID 14300 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 178508725 | HCID 178508725 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-(4-amino-3-iodo-1H-pyrazolo[3,4-d]pyrimidin-1-yl)-1-pyridiniumolate | HCID 22347252 | 57.9% |
Reaction Conditions
| Temperature | 100 °C |
|---|
Reaction Steps
A solution of 3-iodo-1H-pyrazolo[3,4-d]pyrimidin-4-amine (5.00 g, 0.019 mol) in N,N-dimethylformamide (50 mL) was reacted with 60% sodium hydride in oil (0.92 g, 0.023 mol) at ambient temperature. The mixture was stirred for 15 minutes, and 4-nitropyridine-N-oxide (5.37 g, 0.038 mol) was added. The mixture was heated at 100° C. for 18 hours. The precipitate which formed was filtered, washing with N,N-dimethylformamide and ethyl acetate to give 4-(4-amino-3-iodo-1H-pyrazolo[3,4-d]pyrimidin-1-yl)-1-pyridiniumolate (3.79 g, 0.011 mol) as a tan solid:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07332497B2 |
| Source dataset | uspto-grants-2008_02 |
| ORD ID | ord-bd6e550336a043b0863b397cf91ba1ca |
| Source note | uspto-grants-2008_02 |