HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1004823Generated: October 31, 2026
Trifluoroacetic acid → HCID 54042469, compound
https://huagongshe.com/reaction/1004823
Participants
| Role | Name | HCID | Charge |
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| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | HCID 21967689 | HCID 21967689 | — |
| Product | HCID 54042469 | HCID 54042469 | — |
Reaction Steps
A mixture of (S)-(-)-4-[4-[5-[(acetylamino)methyl]-2-oxo-3-oxazolidinyl]-2,6-difluorophenyl]-1-piperidinecarboxylic 1,1-dimethylethyl ester ((EXAMPLE 35, Step 7, 847 mg) and trifluoroacetic acid (12 mL) maintained at 0° C. under N2 is stirred for two hours and then concentrated under reduced pressure to remove excess trifluoroacetic acid. The residue is diluted with saturated aqueous potassium carbonate (70 mL) and methylene chloride (50 mL), and the layers are separated. The aqueous phase is extracted with methylene chloride (2×50 mL), and the combined organic phase is dried over anhydrous sodium sulfate, concentrated under reduced pressure, triturated with diethyl ether and recrystallized from ethyl acetate to give the title compound, NMR (CDCl3, 400 MHz) 7.08, 6.10, 4.78, 4.00, 3.74, 3.64, 3.19, 3.07, 2.72, 2.03, 1.99, 1.68 δ.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06051716 |
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| Source dataset | uspto-grants-2000_04 |
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| ORD ID | ord-4b5f39b568e54f9488dd3ca692e504fa |
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| Source note | uspto-grants-2000_04 |
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