Water → HCID 59837315, compound

HRID 2356236Notes

Reaction equation

HRID 2356236 reaction equation
[CH2:1]([O:8][C:9]1[CH:10]=[C:11]([S:15][C:16]2[CH:21]=[CH:20][C:19]([CH2:22][CH2:23][C:24]([NH:42][C:43]([O:45][C:46]([CH3:49])([CH3:48])[CH3:47])=[O:44])([CH2:33][O:34][Si](C(C)(C)C)(C)C)[CH2:25][O:26][P:27]([O:31][CH3:32])([O:29][CH3:30])=[O:28])=[C:18]([Cl:50])[CH:17]=2)[CH:12]=[CH:13][CH:14]=1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[F-].C([N+](CCCC)(CCCC)CCCC)CCC.O>C1COCC1>[CH2:1]([O:8][C:9]1[CH:10]=[C:11]([S:15][C:16]2[CH:21]=[CH:20][C:19]([CH2:22][CH2:23][C:24]([NH:42][C:43]([O:45][C:46]([CH3:48])([CH3:47])[CH3:49])=[O:44])([CH2:33][OH:34])[CH2:25][O:26][P:27]([O:29][CH3:30])([O:31][CH3:32])=[O:28])=[C:18]([Cl:50])[CH:17]=2)[CH:12]=[CH:13][CH:14]=1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1

Participants

5

Procedure

To a THF solution (30 mL) of the compound of Example 243 (2.70 g), 1 mol/L tetrabutylammonium fluoride in THF (5 mL) was added and the mixture was stirred for 1 hour at room temperature. Following addition of water, the mixture was extracted with ethyl acetate. The extract was washed with a saturated aqueous solution of sodium chloride and the organic phase was dried over anhydrous sodium sulfate. The solvent was removed by distillation and the residue was purified on a silica gel column chromatography (hexane:ethyl acetate=2:1) to obtain the desired product as a colorless oil (2.30 g).

Workup

  1. extractionthe mixture was extracted with ethyl acetate
  2. washThe extract was washed with a saturated aqueous solution of sodium chloride
  3. dry with materialthe organic phase was dried over anhydrous sodium sulfate
  4. customThe solvent was removed by distillation
  5. customthe residue was purified on a silica gel column chromatography (hexane:ethyl acetate=2:1)

Sources & evidence

ORD record
ord-e518e2db9d724e0a884542f7696a0d17
Source dataset
uspto-grants-2010_07
Patent number
US07759326B2

Reaction notes

Loading…