Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | HCID 19421437 | HCID 19421437 | — |
| Product | HCID 19421444 | HCID 19421444 | 90% |
Reaction Steps
A mixture of 1.5 g (~4.7 mmol) of 4-chloro-1-ethoxycarbonyl-7-nitro[1,2,4]triazolo[4,3-a]quinoxaline and 25 ml of glacial acetic acid was refluxed for 60 min. After cooling to 25° C. the precipitate was filtered off to give 1.5 g of a crude product. Purification by column chromatography (silica gel; eluent: ethyl acetate) gave 1.2 g (~90%) of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05559106 |
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| Source dataset | uspto-grants-1996_09 |
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| ORD ID | ord-05fbc15c66eb4ca7912a1b17abe5e2ce |
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| Source note | uspto-grants-1996_09 |
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