HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2393393Generated: October 30, 2026
HCID 70205854, compound → HCID 18975410, compound
https://huagongshe.com/reaction/2393393
Participants
| Role | Name | HCID | Charge |
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| Reactant | HCID 70205854 | HCID 70205854 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 18975410 | HCID 18975410 | 90.4% |
Reaction Steps
3 g of 10-(3-nitrobenzylidene)-5H-imidazo-(1,2-a]indeno[1,2-e]pyrazin-4-one are hydrogenated at atmospheric pressure and at 50° C. in the presence of 10% palladium-on-charcoal in 100 ml of dimethylformamide. After 20 hours of reaction, the reaction medium is filtered on Celite. The insoluble material is washed with 1 liter of dimethyl sulphoxide and the filtrate is concentrated to dryness under reduced pressure. After drying of the yellow powder thus obtained (5 mmHg; 0.65 kPa) at 65° C., 2.5 g of 10-(3-aminobenzyl)-5H,10H-imidazo[1,2-a]indeno[1,2-e]pyrazin-4-one are obtained, the melting point of which is greater than 260° C. (Analysis, C20H16N4O.0.52 H2O.0.30 DMSO; % calculated C: 73.16; H: 4.91; N: 17.06; % found C: 73.2; H: 5.1; N: 17.2).
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-fafe757145b6445d8b52e3fb8deb60ee |
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| Source note | uspto-grants-1998_09 |
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