Reaction equation
[CH3:1][O:2][C:3]1[CH:4]=[C:5]([CH:52]=[C:53]([O:57][CH3:58])[C:54]=1[O:55][CH3:56])[C:6]([N:8]1[CH2:12][CH2:11][C:10]([CH2:21][CH2:22][N:23]2[CH2:28][CH2:27][CH:26]([NH:29][C:30]3[N:34]([CH2:35][C:36]4[N:37](CC5C=CC=CC=5)[CH:38]=[CH:39][N:40]=4)[C:33]4[CH:48]=[CH:49][CH:50]=[CH:51][C:32]=4[N:31]=3)[CH2:25][CH2:24]2)([C:13]2[CH:18]=[CH:17][C:16]([F:19])=[C:15]([F:20])[CH:14]=2)[CH2:9]1)=[O:7].C([O-])=O.[NH4+]>CO.[Pd]>[CH3:58][O:57][C:53]1[CH:52]=[C:5]([CH:4]=[C:3]([O:2][CH3:1])[C:54]=1[O:55][CH3:56])[C:6]([N:8]1[CH2:12][CH2:11][C:10]([CH2:21][CH2:22][N:23]2[CH2:28][CH2:27][CH:26]([NH:29][C:30]3[N:34]([CH2:35][C:36]4[NH:40][CH:39]=[CH:38][N:37]=4)[C:33]4[CH:48]=[CH:49][CH:50]=[CH:51][C:32]=4[N:31]=3)[CH2:25][CH2:24]2)([C:13]2[CH:18]=[CH:17][C:16]([F:19])=[C:15]([F:20])[CH:14]=2)[CH2:9]1)=[O:7]Participants
5
Reactant 2
Product 1
Reagents, catalysts & solvents 2
Procedure
Combine 1-(3,4,5-trimethoxybenzoyl)-3-(2-(4-(1-(1-benzyl-1H-imidazol-2-ylmethyl)-1H-benzimidazol-2-yl-amino)piperidin-1-yl)ethyl)-3-(3,4-difluorophenyl) pyrrolidine (5 mmol) and 10% palladium-on-carbon (1.5 g) in methanol (50 mL). Add anhydrous ammonium formate (25 mmol). Heat to reflux. After 18 hours, filter, rinse with dichloromethane, and evaporate the filtrate in vacuo to give the title compound.
Workup
- temperatureHeat to reflux
- filtrationfilter
- washrinse with dichloromethane
- customevaporate the filtrate in vacuo
Sources & evidence
- ORD record
- ord-87aa56e966bd4303b7547e00eb71c990
- Source dataset
- uspto-grants-2001_04
- Patent number
- US06211199B1
Linked notes
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