HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Naphthaldehyde → 3-[1-Naphthalen-1-yl-methylidene]-imidazo[1,2-a]pyridin-2-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Naphthaldehyde | HCID 6195 | — |
| Reactant | Imidazo[1,2-a]pyridin-2(3H)-one hydrobromide | HCID 44121307 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 3-[1-Naphthalen-1-yl-methylidene]-imidazo[1,2-a]pyridin-2-one | HCID 68699547 | — |
Reaction Steps
A mixture of 1 g (4.7 mmol) of imidazo[1,2-a]pyridin-2-one hydrobromide salt and 726 mg (4.7 mmol) of 1-naphthaldehyde in 20 mL of ethanol is heated at reflux for 1 h and then cooled to room temperature. The precipitate is collected. The isolated solid is suspended in 40 mL of 2M potassium carbonate solution and the resulting mixture is stirred for 48 h at room temperature. The precipitated solid is collected and washed with water 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-f0f06ba9212746fab22dcc4750bb68b5 |
| Source note | uspto-grants-2012_06 |