Hydrochloric Acid → 3-{1-(4-Fluorophenyl)-3-[3-(4-fluorophenyl)-3-hydroxypropyl]-4-oxoazetidin-2-yl}benzonitrile
Reaction equation
Cl.[Si]([O:9][CH:10]([C:33]1[CH:38]=[CH:37][C:36]([F:39])=[CH:35][CH:34]=1)[CH2:11][CH2:12][CH:13]1[C:16](=[O:17])[N:15]([C:18]2[CH:23]=[CH:22][C:21]([F:24])=[CH:20][CH:19]=2)[CH:14]1[C:25]1[CH:26]=[C:27]([CH:30]=[CH:31][CH:32]=1)[C:28]#[N:29])(C(C)(C)C)(C)C.C(=O)(O)[O-].[Na+]>CO>[F:24][C:21]1[CH:22]=[CH:23][C:18]([N:15]2[C:16](=[O:17])[CH:13]([CH2:12][CH2:11][CH:10]([C:33]3[CH:38]=[CH:37][C:36]([F:39])=[CH:35][CH:34]=3)[OH:9])[CH:14]2[C:25]2[CH:26]=[C:27]([CH:30]=[CH:31][CH:32]=2)[C:28]#[N:29])=[CH:19][CH:20]=1Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
10 ml of 1N hydrochloric acid are added to 7.8 g of 3-[3-[3-(tert-butyldimethyl-silanyloxy)-3-(4-fluorophenyl)propyl]-1-(4-fluorophenyl)-4-oxoazetidin-2-yl]benzonitrile (13) in 200 ml of methanol, and the mixture is stirred for 12 h. Aqueous sodium bicarbonate solution is added to the reaction mixture, which is then extracted with methylene chloride. The organic phase is dried over magnesium sulfate, concentrated and purified by silica gel chromatography (ethyl acetate/heptane=1/3%→1/1). This gives 14: C25H20F2N2O2 (418.45) MS (ESI) 401 (M+H—H2O)
Workup
- extractionis then extracted with methylene chloride
- dry with materialThe organic phase is dried over magnesium sulfate
- concentrationconcentrated
- custompurified by silica gel chromatography (ethyl acetate/heptane=1/3%→1/1)
Sources & evidence
- ORD record
- ord-c3a9de2a7ae946068f62692615885799
- Source dataset
- uspto-grants-2010_03
- Patent number
- US07674773B2
Reaction notes
Loading…