Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | 1-Chloro-4-(chloromethyl)benzene | HCID 7723 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 178483568 | HCID 178483568 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 86744719 | HCID 86744719 | — |
Reaction Steps
In 20 ml of dimethylformamide were suspended 6.0 g of 3-[4-(3-dimethylaminopropoxy)phenyl]-1H-pyrazolo[3,4-b]pyridine and 4.1 g of potassium carbonate. While the mixture was stirred under heating at 50° C., 3.9 g of 4-chlorobenzylchloride dissolved in 5 ml of toluene was added. After the mixture was stirred at 50° C. for 1 hour, the mixture was extracted with toluene-water. The organic layer was concentrated. By adding maleic acid to the residue, the salt was obtained. The obtained crude crystals were recrystallized from ethanol to give 4.5 g of 1-(4-chlorobenzyl)-3-[4-(3-dimethylaminopropoxy)phenyl]-1H-pyrazolo[3,4-b]pyridine·maleate, m.p. 136°-138° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05006520 |
|---|
| Source dataset | uspto-grants-1991_04 |
|---|
| ORD ID | ord-caa3e371da694f46b7adfaacfded1cb2 |
|---|
| Source note | uspto-grants-1991_04 |
|---|