HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl 2-(2-iminopyridin-1(2H)-yl)acetate hydrobromide → Imidazo[1,2-a]pyridin-2(3H)-one--hydrogen bromide (1/1)
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl 2-(2-iminopyridin-1(2H)-yl)acetate hydrobromide | HCID 68699194 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Imidazo[1,2-a]pyridin-2(3H)-one--hydrogen bromide (1/1) | HCID 44121307 | — |
Reaction Steps
A solution of 9 g (34.4 mmol) of (2-imino-2H-pyridin-1-yl)-acetic acid ethyl ester hydrobromide salt in 200 mL of ethanol is heated at reflux for 18 h. The reaction mixture is then cooled to room temperature and the precipitate is collected. The isolated solid is washed with ethanol to give the desired compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08193214B2 |
| Source dataset | uspto-grants-2012_06 |
| ORD ID | ord-4312b25132944418ae79d67d6590fecd |
| Source note | uspto-grants-2012_06 |