HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2080680Generated: October 30, 2026
Trifluoroacetic acid → HCID 67110334, compound
https://huagongshe.com/reaction/2080680
Participants
| Role | Name | HCID | Charge |
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| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | Potassium Nitrate | HCID 24434 | — |
| Reactant | HCID 57433640 | HCID 57433640 | — |
| Product | HCID 67110334 | HCID 67110334 | 95.2% |
Reaction Steps
126 mg of potassium nitrate was added to a trifluoroacetic acid (3 ml) solution of 117 mg of N-{4-{[6-(5-methyl-1,2,4-oxadiazol-3-yl)pyridin-3-yl]oxy}-2-[(2-oxopyrrolidin-1-yl)methyl]phenyl}pyridine-2-carboxamide, and stirred under heat at 80° C. for 7 hours. Trifluoroacetic acid was evaporated away under reduced pressure, then chloroform was added to the residue, and washed with aqueous saturated sodium hydrogencarbonate solution. The organic layer was dried, and the solvent was evaporated away under reduced pressure to obtain 122 mg of N-{4-{[6-(5-methyl-1,2,4-oxadiazol-3-yl)pyridin-3-yl]oxy}-2-nitro-6-[(2-oxopyrrolidin-1-yl)methyl]phenyl}pyridine-2-carboxamide as a brown oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07932394B2 |
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| Source dataset | uspto-grants-2011_04 |
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| ORD ID | ord-612c0a4b733a4df78c3358c71adcb89e |
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| Source note | uspto-grants-2011_04 |
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