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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1004823Generated: October 31, 2026

Trifluoroacetic acid → HCID 54042469, compound

https://huagongshe.com/reaction/1004823

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 21967689HCID 21967689—
ProductHCID 54042469HCID 54042469—

Reaction Conditions

Temperature0 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06051716
Source datasetuspto-grants-2000_04
ORD IDord-4b5f39b568e54f9488dd3ca692e504fa
Source noteuspto-grants-2000_04