Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Diethylaminoethyl chloride | HCID 13364 | — |
| Reactant | HCID 15158064 | HCID 15158064 | — |
| Product | HCID 86744714 | HCID 86744714 | — |
Reaction Steps
In 60 ml of dimethylformamide were suspended 4.0 g of 3-(4-bromophenyl)-1-(4-hydroxyphenyl)-1H-pyrazolo[3,4-b]pyridine, 1.8 g of 2-diethylaminoethylchloride and 1.7 g of potassium carbonate. The mixture was stirred at 100° C. for 6 hours. After the solvent was distilled off under reduced pressure, the residue was extracted with toluene-water. The organic layer was concentrated. By adding maleic acid, the residue was corverted into the salt. The obtained crude crystals were recrystallized from ethyl acetate to give 3.0 g of 3-(4-bromophenyl)-1-[4-(2-diethylaminoethoxy)phenyl]-1H-pyrazolo[3,4-b]pyridine·maleate, m.p. 135°-140° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05006520 |
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| Source dataset | uspto-grants-1991_04 |
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| ORD ID | ord-451219abdd6344cfa4ed884f82eb0727 |
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| Source note | uspto-grants-1991_04 |
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