HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → 5-phenylvalerylamino-5H,10H-imidazo[1,2-a]indeno[1,2-e]pyrazine-4-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Benzenepentanoic acid | HCID 16757 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 8-amino-5H,10H-imidazo[1,2-a]indeno[1,2-e]pyrazine-4-one | HCID 18975394 | — |
| Product | 5-phenylvalerylamino-5H,10H-imidazo[1,2-a]indeno[1,2-e]pyrazine-4-one | HCID 86752968 | — |
Reaction Steps
The preparation is carried out as in Example 12, from 5 g of 5-phenylvaleric acid, 2.5 ml of thionyl chloride, 60 ml of dichloromethane, 1 g of 8-amino-5H,10H-imidazo[1,2-a]indeno[1,2-e]pyrazine-4-one and 75 ml of dimethylformamide. After refluxing for 7 hours, the insoluble material is filtered and recrystallized from dimethylformamide. After filtration, washing with water and drying under reduced pressure (1 mm Hg, 0.13 kPa) at 80° C., there is obtained 0.58 g of 8-(5-phenylvalerylamino-5H,10H-imidazo[1,2-a]indeno[1,2-e]pyrazine-4-one in the form of a yellow solid which decomposes at 170° C. (Analysis C24H22N4O2.0.41DMF, % calculated C: 72.34, H: 5.56, N: 14.06, % found C: 72.0, H: 5.6, N: 13.8).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05789406 |
| Source dataset | uspto-grants-1998_08 |
| ORD ID | ord-3d88c839167a4ddaaf5796f47fd5cd1a |
| Source note | uspto-grants-1998_08 |