HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Bromophenol → 5-(4-Bromophenoxy)-1-phenyl-1H-pyrazolo[3,4-b]pyrazine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Bromophenol | HCID 7808 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 5-Chloro-1-phenyl-1H-pyrazolo[3,4-b]pyrazine | HCID 13271936 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | 5-(4-Bromophenoxy)-1-phenyl-1H-pyrazolo[3,4-b]pyrazine | HCID 13271949 | 89% |
Reaction Conditions
| Temperature | 100 °C |
|---|
Reaction Steps
In 3 ml of dimethyl sulfoxide were dissolved 2.00 g (0.0115 mole) of p-bromophenol and 0.5 g (0.009 mole) of potassium hydroxide, and 1.00 g (0.0043 mole) of 5-chloro-1-phenyl-1H-pyrazolo[3,4-b]pyrazine was added to the solution. The mixture was maintained at 100° C. for 2 hours. The post treatments were conducted in the same manner as described in Example 39, and the resulting residue was recrystallized from hexane to obtain 1.41 g (the yield was 89%) of 5-(4-bromophenoxy)-1-phenyl-1H-pyrazolo[3,4-b]pyrazine in the form of a colorless scaly crystal.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04460773 |
| Source dataset | uspto-grants-1984_07 |
| ORD ID | ord-ac4511943e424983903f0893eb21d443 |
| Source note | uspto-grants-1984_07 |