HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,4-Dibromobutane → 5H,10H-imidazo[1,2-a]indeno[1,2-e]pyrazine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,4-Dibromobutane | HCID 8056 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 5H,10H-imidazo[1,2-a]indeno[1,2-e]pyrazin-4-one | HCID 10353549 | — |
| Catalyst | Tetrabutylammonium Bromide | HCID 74236 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | 5H,10H-imidazo[1,2-a]indeno[1,2-e]pyrazine | HCID 131720656 | — |
Reaction Steps
The procedure is performed as in Example 9, but starting with 1.1 g of 5H,10H-imidazo[1,2-a]indeno-[1,2-e]pyrazin-4-one, 40 ml of dimethyl sulphoxide, 2 g of sodium hydroxide pellets, 32 mg of tetrabutylammonium bromide and 0.6 ml of 1,4-dibromobutane. After drying at 80° C., 0.17 g of spiro[5H,10H-imidazo[1,2-a]indeno[l,2-e]pyrazine-10:1'-cyclopentane]-4-one is obtained, in the form of a white solid melting above 260° C. (Analysis % calculated C: 73.63, H: 5.45, N: 15.15, O: 5.77, % found C: 73.8, H: 5.8, N: 15.1, O: 6.0).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05753657 |
| Source dataset | uspto-grants-1998_05 |
| ORD ID | ord-dbf8d9ad7a874a66bfbc50ff6bbc3020 |
| Source note | uspto-grants-1998_05 |