Water → Ammonia
Reaction equation
[H-].[Na+].[C:3]([O:7][C:8](=[O:26])[CH2:9][N:10]1[CH2:15][CH2:14][CH:13]([C:16]2[C:24]3[C:19](=[CH:20][C:21]([Br:25])=[CH:22][CH:23]=3)[NH:18][N:17]=2)[CH2:12][CH2:11]1)([CH3:6])([CH3:5])[CH3:4].[F:27][C:28]1[CH:35]=[CH:34][C:31]([CH2:32]Br)=[CH:30][CH:29]=1.O>CN(C=O)C>[NH3:10].[C:3]([O:7][C:8](=[O:26])[CH2:9][N:10]1[CH2:11][CH2:12][CH:13]([C:16]2[C:24]3[C:19](=[CH:20][C:21]([Br:25])=[CH:22][CH:23]=3)[N:18]([CH2:32][C:31]3[CH:34]=[CH:35][C:28]([F:27])=[CH:29][CH:30]=3)[N:17]=2)[CH2:14][CH2:15]1)([CH3:6])([CH3:4])[CH3:5]Participants
Reactant 4
Product 2
Reagents, catalysts & solvents 1
Procedure
Sodium hydride (42 mg of a 60% dispersion in oil, 1.05 mmol) was added to a stirred solution of [4-(6-bromo-1H-indazol-3-yl)-piperidin-1-yl]-acetic acid tert-butyl ester (332 mg, 0.84 mmol) in DMF (7 ml) and after 30 min, a solution of 4-fluorobenzyl bromide (0.105 ml, 0.84 mmol), in DMF (7 ml) was added. The mixture stirred at +23° under nitrogen for 16 h, treated with water (25 ml), extracted with ethyl acetate (3×50 ml) and the combined, dried (Na2SO4) organic extracts were evaporated in vacuo to give an oil. This oil was purified by flash chromatography over silica gel (Merck 9385) eluting with dichloromethane--ethanol--880 ammonia (967:30:3) to give impure title compound. This was further purified by flash chromatography over silica gel (Merck 9385) eluting with ethyl acetate--cyclohexane (1:2) to give the title compound as a colourless oil (290 mg).
Workup
- extractionextracted with ethyl acetate (3×50 ml)
- dry with materialdried (Na2SO4) organic extracts
- customwere evaporated in vacuo
- customto give an oil
- customThis oil was purified by flash chromatography over silica gel (Merck 9385)
- washeluting with dichloromethane
Sources & evidence
- ORD record
- ord-095fa4bcef114249aae3b31cd812c4d0
- Source dataset
- uspto-grants-1999_01
- Patent number
- US05861414
Reaction notes
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