HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1084837Generated: October 25, 2026
Potassium Carbonate → N,N-diethyl-3-[3-(4-fluorophenyl)-1H-pyrazolo[3,4-b]pyridin-1yl]phenoxyacetamide
https://huagongshe.com/reaction/1084837
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-bromo-N,N-diethylacetamide | HCID 225545 | — |
| Reactant | 3-(4-fluorophenyl)-1-(3-hydroxyphenyl)-1H-pyrazolo[3,4-b]pyridine | HCID 14796258 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | N,N-diethyl-3-[3-(4-fluorophenyl)-1H-pyrazolo[3,4-b]pyridin-1yl]phenoxyacetamide | HCID 14796274 | 40.9% |
Reaction Steps
In 75 ml of dimethylformamide were suspended 5.0 g of 3-(4-fluorophenyl)-1-(3-hydroxyphenyl)-1H-pyrazolo[3,4-b]pyridine, 3.5 g of N,N-diethylbromoacetamide and 2.5 g of potassium carbonate. The mixture was stirred at 60° C. for 5 hours. After the solvent was distilled off under reduced pressure, the residue was extracted with ethyl acetate-water. The organic layer was concentrated. Isopropyl ether was added to the residue for crystallization. The obtained crude crystals were recrystallized from ethyl acetate to give 2.8 g of N,N-diethyl-3-[3-(4-fluorophenyl)-1H-pyrazolo[3,4-b]pyridin-1yl]phenoxyacetamide, m.p. 102°-105° 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-2d06a56142c04d5bbfddb29f84459f6c |
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| Source note | uspto-grants-1991_04 |
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