HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Aminopyridine → 2-Butylimidazo(1,2-a)pyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Aminopyridine | HCID 10439 | — |
| Reactant | 1-Bromohexan-2-one | HCID 12431733 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 2-Butylimidazo(1,2-a)pyridine | HCID 15129907 | 53.1% |
Reaction Steps
A mixture of 6 g of 2-amino pyridine and 60 ml of anhydrous acetone was added to a mixture of 16 g of the product of Stage B and 20 ml of acetone at ambient temperature. The mixture was refluxed for one hour and the acetone was partially distilled. The mixture was allowed to return to ambient temperature, ice-cooled, separated and washed with ethyl ether. The insoluble part was dissolved in a saturated solution of sodium carbonate and extraction was carried out with ethyl acetate. The extracts were washed with water saturated in sodium chloride, dried and filtered to obtain 5.9 g of the expected product in the form of a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05420138 |
| Source dataset | uspto-grants-1995_05 |
| ORD ID | ord-0a296b96e6cb4a569488c76c832ec44c |
| Source note | uspto-grants-1995_05 |