Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Acetic acid, 2-chloro-, phenylmethyl ester | HCID 8786 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 178483568 | HCID 178483568 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 14796402 | HCID 14796402 | — |
Reaction Steps
To a suspension of 9 g of 3-[4-(3-dimethylaminopropoxy)phenyl]-1H-pyrazolo[3,4-b]pyridine, 30 ml of dimethylformamide and 6.2 g of potassium carbonate was added dropwise 6.6 g of benzyl chloroacetate at 50° C. over the period of 2 hours. The mixture was kept at the same temperature for 4 hours. After the completion of the reaction, the reaction mixture was cooled. Water was added thereto, and the mixture was extracted with toluene. The extract was washed with water. After toluene was distilled off, diisopropyl ether was added to the residue for crystallization. The resulting crystals were recrystallized from diisopropyl ether - ethyl acetate to give benzyl 3-[4-(3-dimethylaminopropoxy)phenyl]-1H-pyrazolo[3,4-b]pyridin-1-ylacetate, m.p. 90°-92° 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-21ebf5f8bff3437da3f74bfabf5a4449 |
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| Source note | uspto-grants-1991_04 |
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