HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1864991Generated: October 25, 2026
1,2-Dibromoethane → 7-Bromo-2-ethyl-4-methoxypyrazolo[1,5-a]pyridine
https://huagongshe.com/reaction/1864991
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,2-Dibromoethane | HCID 7839 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 2-Ethyl-4-methoxypyrazolo[1,5-a]pyridine | HCID 21984578 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 7-Bromo-2-ethyl-4-methoxypyrazolo[1,5-a]pyridine | HCID 21984567 | — |
Reaction Steps
n-Butyllithium (1.31 mL) was slowly added dropwise to a solution of 2-ethyl-4-methoxypyrazolo[1,5-a]pyridine (303 mg) in tetrahydrofuran (15 mL) at −78° C. After stirring the mixture at −78° C. for 1 hour, 1,2-dibromoethane (0.18 mL) was added and stirring was continued for 1 hour. Saturated aqueous ammonium chloride was added, extraction was performed with ethyl acetate, the extract washed with brine and dried over magnesium sulfate, and the solvent was distilled off under reduced pressure. The residue was subjected to silica gel column chromatography (20 g), and the title compound (282 mg) was obtained from the n-hexane:ethyl acetate (5:1) fraction as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07625925B2 |
|---|
| Source dataset | uspto-grants-2009_12 |
|---|
| ORD ID | ord-36c761d88e6d4f768136cecaec694884 |
|---|
| Source note | uspto-grants-2009_12 |
|---|