Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzaldehyde | HCID 240 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 400200 | HCID 400200 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 400202 | HCID 400202 | 83% |
Reaction Steps
Compound A (3.51 g) was added to a 40 mL of dimethylformamide solution containing equal molar of benzaldehyde and 4 equivalents of triethylamine. The solution was refluxed at 60° C. for 16 hr and cooled at ice bath to produce a yellow precipitate. The precipitate was then collected and washed with ethyl acetate to give 3.3 g (83%) of the desired product 3-[(5-benzyloxypyridin-2-yl)methylidene]-6-phenylmethylidenepiperazine-2,5-dione (Compound 1) as a mixture of isomers. The mixture was predominately the ZZ and EZ isomers.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07288545B2 |
|---|
| Source dataset | uspto-grants-2007_10 |
|---|
| ORD ID | ord-16d9e7cb65df49848e00d1b3217a09f8 |
|---|
| Source note | uspto-grants-2007_10 |
|---|