HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2393361Generated: October 30, 2026
Ethyl trifluoroacetate → HCID 140392638, compound
https://huagongshe.com/reaction/2393361
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethyl trifluoroacetate | HCID 9794 | — |
| Reactant | 10-Amino-5H,10H-imidazo[1,2-a]indeno-[1,2-e]pyrazin-4-one | HCID 15291362 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 140392638 | HCID 140392638 | 12.1% |
Reaction Steps
To a suspension of 0.5 g of 10-amino-5H,10H-imidazo[1,2-a]indeno[1,2-e]pyrazin-4-one in 15 ml of dimethylformamide is added 0.6 ml of ethyl trifluoroacetate at a temperature in the region of 20° C. The reaction medium is heated at 60° C. for 5 hours and is then cooled and concentrated to dryness under reduced pressure (15 mmHg; 2 kPa). The residue is taken up in dichloromethane and the insoluble product is filtered off, washed and dried. After purification by flash chromatography using a mixture of ethyl acetate and methanol (90/10 by volume) as eluent, 0.06 g of 10-imino-5H,10H-imidazo[1,2-a]indeno[1,2-e]pyrazin-4-one is obtained in the form of a reddish powder, the melting point of which is greater than 260° C. (NMR spectrum: [200 MHz; (CD3)2SO-d6 ; δ in ppm]: from 7.20 to 7.50 (mt, 2H: --H 7 and --H 8); 7.57 and 8.33 (2s, 1H each: --H of the imidazole); 7.65 and 7.86 (2 broad d, J=8 Hz, 1H each: --H 6 and --H 9); from 11.10 to 12.10 (broad mult., 1H: --CONH--)).
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-4d41168c18c44548b773598e64a27dd2 |
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| Source note | uspto-grants-1998_09 |
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