HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1181862Generated: October 25, 2026
Ethyl Acetate → 7-(2-Chloro-4-methoxyphenyl)-2-ethyl-3-nitropyrazolo[1,5-a]pyridine
https://huagongshe.com/reaction/1181862
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Barium hydroxide, octahydrate | HCID 17749109 | — |
| Reactant | 7-Bromo-2-ethyl-3-nitropyrazolo[1,5-a]pyridine | HCID 21984481 | — |
| Reactant | 2-Chloro-4-methoxyphenylboric acid | HCID 21984696 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | 1,2-Dimethoxyethane | HCID 8071 | — |
| Product | 7-(2-Chloro-4-methoxyphenyl)-2-ethyl-3-nitropyrazolo[1,5-a]pyridine | HCID 21984583 | 73.3% |
Reaction Steps
After dissolving 7-bromo-2-ethyl-3-nitropyrazolo[1,5-a]pyridine (100 mg) in 1,2-dimethoxyethane (6 mL) and water (1 mL), 2-chloro-4-methoxyphenylboric acid (138 mg), tetrakis(triphenylphosphine)palladium (0) complex (86 mg) and barium hydroxide octahydrate (233 mg) 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 extract was washed with saturated aqueous sodium hydrogencarbonate and brine, in that order. 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 (90 mg) was obtained from the n-hexane:ethyl acetate (30:1) fraction as yellow crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07285666B2 |
|---|
| Source dataset | uspto-grants-2007_10 |
|---|
| ORD ID | ord-edcd07d3923e47119b5739a6e8afda9a |
|---|
| Source note | uspto-grants-2007_10 |
|---|