Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 3-Chloro-N,N-dimethyl-1-propanamine | HCID 66960 | — |
| Reactant | HCID 14796259 | HCID 14796259 | — |
| Product | HCID 86744713 | HCID 86744713 | — |
Reaction Steps
In 100 ml of dimethylformamide were suspended 7.0 g of 1-(4-hydroxyphenyl)-3-phenyl-1H-pyrazolo[3,4-b]pyridine, 3.6 g of 3-dimethylaminopropylchloride and 3.7 g of potassium carbonate. The mixture was stirred at 100° C. for 4 hours. After the solvent was distilled off under reduced pressure, the residue was extracted with chloroform-water. The organic layer was concentrated, and the residue was purified by silica gel column chromatography (eluent: chloroform : methanol=20:1). Thereafter, by adding maleic acid, the purified product was converted into the salt. The obtained crude crystals were recrystallized from ethyl acetate to give 7.2 g of 1-[4-(3-dimethylaminopropoxy)phenyl]-3-phenyl-1H-pyrazolo[3,4-b]pyridine·maleate, m.p. 133°-136° 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-a8d85c776d384bfdb53be66d42c9d2ee |
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| Source note | uspto-grants-1991_04 |
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