HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 67260280, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | sec-Butylhydrazine | HCID 547690 | — |
| Reactant | HCID 65583291 | HCID 65583291 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 67260280 | HCID 67260280 | 21% |
| Product | HCID 67260571 | HCID 67260571 | 16% |
Reaction Steps
A mixture of 1-(5-chloro-2-thienyl)-2-(pyridin-4-yl)ethanone (0.68 mmol), secbutylhydrazin (1.37 mmol) and triethylamine (1.37 mmol) in 5 mL dichloromethane was refluxed for 2.5 h. The solvent was evaporated under reduced pressure and the residue was partitioned between ethyl acetate and water. The aqueous layer was extracted with ethyl acetate and the combined organic extracts were dried over MgSO4 filtered and concentrated. The residue was purified by chromatography on silica gel (dichloromethane:methanol 100:1 to 20:1) to afford 37 mg of 4-[1-sec-butyl-3-(5-chloro-2-thienyl)-1H-pyrazol-4-yl]pyridine (16% yield) and 48 mg of 4-[1-sec-butyl-5-(5-chloro-2-thienyl)-1H-pyrazol-4-yl]pyridine (21% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08685974B2 |
| Source dataset | uspto-grants-2014_04 |
| ORD ID | ord-836c52c166684ccfa282695d0e5143ee |
| Source note | uspto-grants-2014_04 |