HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 9182Generated: October 24, 2026
Water → 7-(2,4-Dichlorophenyl)-2-ethylpyrazolo[1,5-a]pyridine
https://huagongshe.com/en/reaction/9182
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 2,4-Dichlorophenylboric acid | HCID 21984477 | — |
| Reactant | 7-Bromo-2-ethylpyrazolo[1,5-a]pyridine | HCID 21984510 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 7-(2,4-Dichlorophenyl)-2-ethylpyrazolo[1,5-a]pyridine | HCID 21984635 | 97.9% |
Reaction Steps
After dissolving 7-bromo-2-ethylpyrazolo[1,5-a]pyridine (300 mg) in ethanol (2 mL) and toluene (4 mL), 2,4-dichlorophenylboric acid (508 mg), tetrakis(triphenylphosphine)palladium (0) complex (154 mg) and 2 M aqueous sodium carbonate (1.33 mL) were added and the mixture was heated and stirred at 80° C. for 3 hours under a nitrogen stream. Water was added to the reaction mixture, extraction was performed with ethyl acetate and the organic layer was washed with brine. After drying over anhydrous magnesium sulfate and filtration, the solvent was concentrated under reduced pressure, the residue was purified by silica gel column chromatography, and the title compound (380 mg) was obtained from the n-hexane:ethyl acetate (100:1) fraction as a light yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07091215B2 |
|---|
| Source dataset | uspto-grants-2006_08 |
|---|
| ORD ID | ord-f014e611ef1f44afbd81fa386b31f468 |
|---|
| Source note | uspto-grants-2006_08 |
|---|