HCID 86613448, compound → HCID 67279585, compound

HRID 2387577Notes

Reaction equation

HRID 2387577 reaction equation
[CH2:1]([O:8][C:9](=[O:48])[CH2:10][CH2:11][C:12]([O:14][C:15]1([CH2:28][O:29][C:30]2[CH:35]=[CH:34][C:33]([N:36]3[CH2:40][C@H:39]([CH2:41][NH:42][C:43](=[O:45])[CH3:44])[O:38][C:37]3=[O:46])=[CH:32][C:31]=2[F:47])[CH2:20][CH2:19][N:18](OC(C)(C)C)[C:17](=C=O)[CH2:16]1)=[O:13])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1>FC(F)(F)C(O)=O>[CH2:1]([O:8][C:9](=[O:48])[CH2:10][CH2:11][C:12]([O:14][C:15]1([CH2:28][O:29][C:30]2[CH:35]=[CH:34][C:33]([N:36]3[CH2:40][C@H:39]([CH2:41][NH:42][C:43](=[O:45])[CH3:44])[O:38][C:37]3=[O:46])=[CH:32][C:31]=2[F:47])[CH2:20][CH2:19][NH:18][CH2:17][CH2:16]1)=[O:13])[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1

Participants

3

Reactant 1

HCID 86613448HCID 86613448, compound

Product 1

HCID 67279585HCID 67279585, compound

Reagents, catalysts & solvents 1

HCID 6422Trifluoroacetic acidSolvent

Procedure

820 mg of succinic acid 4-{4-[(5S)-5-(acetylamino-methyl)-2-oxo-oxazolidin-3-yl]-2-fluoro-phenoxymethyl}-1-tert-butoxy-carbonyl-piperidin-4-yl ester benzyl ester (MW: 671.72, 1.23 mmol) were dissolved in 4 ml of trifluoro acetic acid. The reaction mixture was stirred at room temperature for one hour. The solvent was evaporated, the residue dissolved in 30 ml of a 9/1 dichloromethane/methanol mixture and the organic layer washed successively with 30 ml of a saturated aqueous sodium bicarbonate solution and 30 ml of brine. The organic layer was dried over magnesium sulfate, filtered and the filtrate evaporated under reduced pressure. The residue was purified by chromatography over silica, using a 95/5 dichloromethane/methanol mixture with 2% triethylamine as eluent. Yield: 420 mg, 60%. MS: 572.7 (M+H)+, Method ESI+.

Workup

  1. customThe solvent was evaporated
  2. dissolutionthe residue dissolved in 30 ml of a 9/1 dichloromethane/methanol mixture
  3. washthe organic layer washed successively with 30 ml of a saturated aqueous sodium bicarbonate solution and 30 ml of brine
  4. dry with materialThe organic layer was dried over magnesium sulfate
  5. filtrationfiltered
  6. customthe filtrate evaporated under reduced pressure
  7. customThe residue was purified by chromatography over silica

Sources & evidence

ORD record
ord-4dddf941e2b24129b3897b3ea21f98d0
Source dataset
uspto-grants-2012_09
Patent number
US08268812B2

Reaction notes

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