Water → HCID 57704525, compound
Reaction equation
[C:1]([O:5][C:6](=[O:36])[NH:7][C:8]([CH2:31][O:32][CH2:33][O:34][CH3:35])([CH2:22][CH2:23][O:24][CH:25]1[CH2:30][CH2:29][CH2:28][CH2:27][O:26]1)[CH2:9][CH2:10][C:11]1[CH:16]=[CH:15][C:14]([OH:17])=[C:13]([C:18]([F:21])([F:20])[F:19])[CH:12]=1)([CH3:4])([CH3:3])[CH3:2].C(=O)([O-])[O-].[K+].[K+].[CH2:43](Br)[CH2:44][CH2:45][CH2:46][CH2:47][CH2:48][CH3:49].O>CN(C)C=O>[C:1]([O:5][C:6](=[O:36])[NH:7][C:8]([CH2:31][O:32][CH2:33][O:34][CH3:35])([CH2:22][CH2:23][O:24][CH:25]1[CH2:30][CH2:29][CH2:28][CH2:27][O:26]1)[CH2:9][CH2:10][C:11]1[CH:16]=[CH:15][C:14]([O:17][CH2:43][CH2:44][CH2:45][CH2:46][CH2:47][CH2:48][CH3:49])=[C:13]([C:18]([F:20])([F:21])[F:19])[CH:12]=1)([CH3:4])([CH3:3])[CH3:2]Participants
6
Reactant 4
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 80 °C
Procedure
Compound 21-6 (1.24 g) was dissolved in N,N-dimethylformamide (20 ml), potassium carbonate (986 mg) and n-heptyl bromide (0.458 ml) were added, and the mixture was stirred at 80° C. for 2.5 hr. Water was added to the reaction mixture, and the mixture was extracted with ethyl acetate, washed with water and saturated brine, and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure to give the object product (1.49 g) as a pale-yellow oil.
Workup
- extractionthe mixture was extracted with ethyl acetate
- washwashed with water and saturated brine
- dry with materialdried over anhydrous magnesium sulfate
- customThe solvent was evaporated under reduced pressure
Sources & evidence
- ORD record
- ord-7de81bec56824c20a8f4e519609addcd
- Source dataset
- uspto-grants-2014_08
- Patent number
- US08809304B2
Reaction notes
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