HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2095759Generated: November 1, 2026
Trifluoroacetic anhydride → HCID 58158576, compound
https://huagongshe.com/reaction/2095759
Participants
| Role | Name | HCID | Charge |
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| Reactant | Trifluoroacetic anhydride | HCID 9845 | — |
| Reactant | HCID 86651396 | HCID 86651396 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 58158576 | HCID 58158576 | 51.4% |
Reaction Steps
To a solution of benzyl (4-{[1-(2-amino-2-oxoethyl)-6-{[(4-methylphenyl)sulfonyl]imino}-1,6-dihydropyridin-3-yl]oxy}-3-fluorophenyl)carbamate (28.0 g, 49.6 mmol) in tetrahydrofuran (280 mL) was added trifluoroacetic acid anhydride (196 mL), and the mixture was stirred at room temperature for 3 hr. The solvent was evaporated under reduced pressure, ethyl acetate/tetrahydrofuran was added to the residue, and the mixture was washed with saturated aqueous sodium hydrogen carbonate and saturated brine in this order, dried over anhydrous magnesium sulfate and filtered. The solvent was evaporated under reduced pressure, ethanol (140 mL) and 4N aqueous sodium hydroxide solution (40 mL) were added to the residue, and the mixture was stirred at room temperature for 4 hr. The solvent was concentrated under reduced pressure to about 1/3, water was added to the residue, and the mixture was extracted with ethyl acetate/tetrahydrofuran. The organic layer was washed with saturated brine, dried over anhydrous magnesium sulfate and filtered. The solvent was evaporated under reduced pressure, and the residue was purified by silica gel column chromatography (ethyl acetate/methanol=10/0→9/1) to give the title compound (10.0 g, 51%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08445509B2 |
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| Source dataset | uspto-grants-2013_05 |
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| ORD ID | ord-347ea5ed47d445539dbcc6eb8900b0df |
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| Source note | uspto-grants-2013_05 |
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