HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1107036Generated: October 31, 2026
HCID 18790675, compound → HCID 18790679, compound
https://huagongshe.com/reaction/1107036
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 18790675 | HCID 18790675 | — |
| Reactant | HCID 67066987 | HCID 67066987 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 18790679 | HCID 18790679 | 97.9% |
Reaction Steps
A mixture of 1 g of 8-aminomethyl-5H,10H-imidazo[1,2-a]indeno[1,2-e]pyrazin-4-one and 1.8 g of 4-nitrophenyl-N-methylcarbamate in 40 ml of dimethylformamide is stirred for 18 hours at a temperature in the region of 20° C. The reaction mixture is filtered and washed with 5 ml of dimethylformamide. The solid is taken up in 25 ml of dimethylformamide and the suspension is heated at 100° C. for 30 minutes. The insoluble material is filtered and washed with 5 ml of dimethylformamide and then with 20 ml of acetone. After drying under reduced pressure (1 mbar) at 60° C., 1.2 g of 8-(3-methylureido)methyl-5H,10H-imidazo[1,2-a]indeno[1,2-e]pyrazin-4-one are obtained in the form of a yellow solid, the melting point of which is greater than 260° C. (Analysis; % Calculated C: 62.13, H: 4.89, N: 22.64; % Found C: 62.0, H: 4.5, N: 22.6).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06057454 |
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| Source dataset | uspto-grants-2000_05 |
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| ORD ID | ord-03c7c8cb479841618219a8fda2f1253b |
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| Source note | uspto-grants-2000_05 |
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