Trifluoroacetic acid → HCID 54042469, compound

HRID 1004823Notes

Reaction equation

HRID 1004823 reaction equation
CC(OC([N:8]1[CH2:13][CH2:12][CH:11]([C:14]2[C:19]([F:20])=[CH:18][C:17]([N:21]3[CH2:25][C@H:24]([CH2:26][NH:27][C:28](=[O:30])[CH3:29])[O:23][C:22]3=[O:31])=[CH:16][C:15]=2[F:32])[CH2:10][CH2:9]1)=O)(C)C.FC(F)(F)C(O)=O>>[O:31]=[C:22]1[N:21]([C:17]2[CH:16]=[C:15]([F:32])[C:14]([CH:11]3[CH2:12][CH2:13][NH:8][CH2:9][CH2:10]3)=[C:19]([F:20])[CH:18]=2)[CH2:25][C@H:24]([CH2:26][NH:27][C:28](=[O:30])[CH3:29])[O:23]1

Participants

3

Reactant 2

HCID 6422Trifluoroacetic acidHCID 21967689HCID 21967689, compound

Product 1

HCID 54042469HCID 54042469, compound

Conditions

Temperature
0 °C

Procedure

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.

Workup

  1. concentrationconcentrated under reduced pressure
  2. customto remove excess trifluoroacetic acid
  3. additionThe residue is diluted with saturated aqueous potassium carbonate (70 mL) and methylene chloride (50 mL)
  4. customthe layers are separated
  5. extractionThe aqueous phase is extracted with methylene chloride (2×50 mL)
  6. dry with materialthe combined organic phase is dried over anhydrous sodium sulfate
  7. concentrationconcentrated under reduced pressure
  8. customtriturated with diethyl ether
  9. customrecrystallized from ethyl acetate

Sources & evidence

ORD record
ord-4b5f39b568e54f9488dd3ca692e504fa
Source dataset
uspto-grants-2000_04
Patent number
US06051716

Reaction notes

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