HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → 10-(3-pyridylmethyl)-5H,10H-imidazo[1,2-a]indeno-[1,2-e]pyrazin-4-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | 10-(3-pyridylmethylene)-5H,10H-imidazo[1,2-a]indeno[1,2-e]pyrazin-4-one | HCID 57286362 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 10-(3-pyridylmethyl)-5H,10H-imidazo[1,2-a]indeno-[1,2-e]pyrazin-4-one | HCID 18918153 | 37.8% |
Reaction Steps
The procedure is performed as in Example 21, but starting with 1 g of 10-(3-pyridylmethylene)-5H,10H-imidazo[1,2-a]indeno[1,2-e]pyrazin-4-one, 150 ml of dimethylformamide, 5 ml of acetic acid and 0.1 g of 10% palladium on charcoal. 0.38 g of 10-(3-pyridylmethyl)-5H,10H-imidazo[1,2-a]indeno-[1,2-e]pyrazin-4-one is obtained, in the form of an off-white solid melting above 260° C. (Analysis % calculated C: 72.60, H: 4.49, N: 17.82, O: 5.09, % found C: 72.3, H: 4.8, N: 17.8, O: 5.4).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05753657 |
| Source dataset | uspto-grants-1998_05 |
| ORD ID | ord-8eed9939a3b54527bf63771d9c3409ab |
| Source note | uspto-grants-1998_05 |