HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → Imidazo[1,2-a]pyridine,5-[(4-chlorobutyl)thio]-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1-Bromo-4-chlorobutane | HCID 81364 | — |
| Reactant | HCID 178418687 | HCID 178418687 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Imidazo[1,2-a]pyridine,5-[(4-chlorobutyl)thio]- | HCID 18936641 | — |
Reaction Steps
In a nitrogen atmosphere, 8.87 ml (77 mmol) of 1-bromo-4-chlorobutane was added to a solution of 10.51 g (70 mmol) of 5-mercaptoimidazo[1,2-a]pyridine and 10.73 ml (77 mmol) of triethylamine in 150 ml of ethanol was added, followed by stirring at room temperature for 16 hours. After the solvent was distilled off, the residue was dissolved in dichloromethane. This solution was washed with saturated aqueous sodium hydrogen carbonate and dried, after which the solvent was distilled off. The residue was purified by column chromatography (eluent: ethyl acetate) to yield 12.93 g (76.7%, light brown oily substance) of the desired product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05840732 |
| Source dataset | uspto-grants-1998_11 |
| ORD ID | ord-afc7370ad75e49a9ac250316b96f5076 |
| Source note | uspto-grants-1998_11 |