Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonium Acetate | HCID 517165 | — |
| Reactant | Methyl 3-formylbenzoate | HCID 639145 | — |
| Reactant | 5H,10H-imidazo[1,2-a]indeno[1,2-e]pyrazin-4-one | HCID 10353549 | — |
| Solvent | Acetic Anhydride | HCID 7918 | — |
| Product | HCID 86753085 | HCID 86753085 | 55.1% |
Reaction Steps
0.5 g of 5H,10H-imidazo[1,2-a]indeno[1,2-e]-pyrazin-4-one and 1.47 g of 3-methoxycarbonyl-benzaldehyde are refluxed for 48 hours in the presence of 0.7 g of ammonium acetate in 30 ml of acetic anhydride. After cooling to a temperature in the region of 20° C., the precipitate formed is filtered off, washed with water and dried under reduced pressure (1 mmHg; 0.13 kPa) at 50° C. 0.53 g of 10-(3-methoxycarbonyl-benzylidene)-5H-imidazo[1,2-a]indeno[1,2-e]pyrazin-4-one acetate is obtained in the form of a yellow powder, the melting point of which is greater than 260° C. (Analysis, C24H19 N3O5.0.19 H2O; % calculated C: 67.13; H: 4.46; N: 9.79; O: 18.63; % found C: 66.9; H: 4.4; N: 9.9; O: 18.6).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05807859 |
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| Source dataset | uspto-grants-1998_09 |
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| ORD ID | ord-469c63ff87d74bf69ad28752e59e63ea |
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| Source note | uspto-grants-1998_09 |
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