2,2,2-Trifluoroethanol → HCID 178441287, compound

HRID 1888631Notes

Reaction equation

HRID 1888631 reaction equation
[CH2:1]([C:5]1=[CH:6][N:7]([C:21]([CH3:24])([CH3:23])[CH3:22])[S:8]/[C:9]/1=[N:10]\[C:11](=[O:20])[C:12]1[CH:17]=[C:16]([Cl:18])[CH:15]=[CH:14][C:13]=1F)[CH2:2][CH2:3][CH3:4].[CH2:25]([OH:30])[C:26]([F:29])([F:28])[F:27].CC(C)([O-])C.[K+]>C1COCC1.O>[F:27][C:26]([F:29])([F:28])[C:25]([OH:20])=[O:30].[CH2:1]([C:5]1=[CH:6][N:7]([C:21]([CH3:24])([CH3:23])[CH3:22])[S:8]/[C:9]/1=[N:10]\[C:11](=[O:20])[C:12]1[CH:17]=[C:16]([Cl:18])[CH:15]=[CH:14][C:13]=1[O:30][CH2:25][C:26]([F:29])([F:28])[F:27])[CH2:2][CH2:3][CH3:4]

Participants

7

Reactant 3

HCID 64092,2,2-TrifluoroethanolHCID 23665647Potassium tert-butoxideHCID 178441283HCID 178441283, compound

Product 2

HCID 6422Trifluoroacetic acidYield 0.1%HCID 178441287HCID 178441287, compoundYield 56.1%

Reagents, catalysts & solvents 2

HCID 962WaterSolventHCID 8028TetrahydrofuranSolvent

Procedure

A mixture of the product from Example 47A (101 mg, 0.27 mmol), trifluoroethanol (33 mg, 0.32 mmol) and potassium tert-butoxide (2 M) (340 μL, 0.68 mmol) in THF (10 mL) was stirred at rt for 12 hrs. The mixture was diluted with water, and extracted with EtOAc. The organic extract was dried (Na2SO4), filtered and concentrated. The residue was purified by reverse phase preparative HPLC on a Waters Symmetry C8 column (25 mm×100 mm, 7 μm particle size) using a gradient of 10% to 100% acetonitrile:0.1% aqueous trifluoroacetic acid over 8 minutes (10 minutes run time) at a flow rate of 40 mL/minute to afford 34 mg (28%) of the title compound. 1H NMR (400 MHz, CDCl3) δ ppm 0.97 (t, J=7.36 Hz, 3 H) 1.37-1.48 (m, 2 H) 1.65-1.75 (m, 2 H) 1.68 (s, 9 H) 4.50 (q, J=8.59 Hz, 2 H) 7.05 (d, J=8.59 Hz, 1 H) 7.34 (dd, J=8.90, 2.76 Hz, 1 H) 7.97 (s, 1 H) 8.11 (d, J=2.76 Hz, 1 H); MS (DCI/NH4+) m/z 449 (M+H)+.

Workup

  1. extractionextracted with EtOAc
  2. extractionThe organic extract
  3. dry with materialwas dried (Na2SO4)
  4. filtrationfiltered
  5. concentrationconcentrated
  6. customThe residue was purified by reverse phase preparative HPLC on a Waters Symmetry C8 column (25 mm×100 mm, 7 μm particle size)

Sources & evidence

ORD record
ord-6788442e50f74970a89790f336ea1095
Source dataset
uspto-grants-2013_08
Patent number
US08501794B2

Reaction notes

Loading…