HuagongsheHuagongshe Chemistry Print Report · For research reference only
Chloroacetic Acid → 2,6-Dichloroimidazo[1,2-A]pyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Chloroacetic Acid | HCID 300 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-Amino-5-chloropyridine | HCID 66174 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 2,6-Dichloroimidazo[1,2-A]pyridine | HCID 11769257 | 11.2% |
Reaction Steps
Chloroacetic acid (9.5 g) is dissolved in 70 ml of acetonitrile, to which 10.1 g of triethylamine is portionwise added and further 12.9 g of 2-amino-5-chloropyrdine is added. The mixture is refluxed for 3 hours. After cooling, the precipitated 2-imino-5-chloro-1,2-dihydropyridin-1-ylacetic acid as crystals is collected by filtration and dried. The crystals are added to 40 ml of phosphorus oxychoride and refluxed for 5 hours. After cooling, the reaction mixture is poured into ice water and neutralized with aqueous ammonia. The precipitate collected by filtration is purified by silica gel chromatography(eluent: ethyl acetate) to give 2.1 g of the title compound as crystals. mp. 155°-156° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05017212 |
| Source dataset | uspto-grants-1991_05 |
| ORD ID | ord-6af8c646c62d43c9b79b756a3afd39ad |
| Source note | uspto-grants-1991_05 |