Acetic Acid → HCID 22238162, compound
Reaction equation
[Cl:1][C:2]1[CH:23]=[CH:22][C:5]([C:6]([NH:8][C:9]2[CH:14]=[C:13]([N:15]3[CH2:20][CH2:19][O:18][CH2:17][CH2:16]3)[CH:12]=[C:11]([F:21])[CH:10]=2)=[O:7])=[CH:4][C:3]=1[NH:24][C:25](=[O:42])[C:26]1[CH:31]=[C:30]([N:32]2[CH2:37][CH2:36][N:35]([CH3:38])[CH2:34][CH2:33]2)[CH:29]=[CH:28][C:27]=1[N+:39]([O-])=O.C(O)(=O)C.C(=O)([O-])[O-].[Na+].[Na+]>[Fe].O.C(O)C>[NH2:39][C:27]1[CH:28]=[CH:29][C:30]([N:32]2[CH2:37][CH2:36][N:35]([CH3:38])[CH2:34][CH2:33]2)=[CH:31][C:26]=1[C:25]([NH:24][C:3]1[CH:4]=[C:5]([CH:22]=[CH:23][C:2]=1[Cl:1])[C:6]([NH:8][C:9]1[CH:14]=[C:13]([N:15]2[CH2:20][CH2:19][O:18][CH2:17][CH2:16]2)[CH:12]=[C:11]([F:21])[CH:10]=1)=[O:7])=[O:42]Participants
Reactant 3
Product 1
Reagents, catalysts & solvents 3
Procedure
Iron powder (0.726 g) was added to a stirred suspension of 4-chloro-N-(3-fluoro-5-morpholinophenyl)-3-[5-(4-methylpiperazin-1-yl)-2-nitrobenzamido]benzamide (0.76 g), water (2 ml), acetic acid (0.5 ml) and ethanol (15 ml) and the resultant mixture was stirred and heated to reflux for 1 hour. The mixture was cooled to ambient temperature. Water (80 ml) was added and the mixture was basified by the addition of sodium carbonate. The resultant mixture was filtered through diatomaceous earth and the separated solids were washed in turn with methylene chloride and methanol. The combined filtrates were evaporated and the residue was triturated under ethyl acetate. The mixture was filtered and the filtrate was evaporated to give the title compound (0.385 g); Mass Spectrum: M+H+ 567.
Workup
- temperatureheated
- temperatureto reflux for 1 hour
- filtrationThe resultant mixture was filtered through diatomaceous earth
- washthe separated solids were washed in turn with methylene chloride and methanol
- customThe combined filtrates were evaporated
- customthe residue was triturated under ethyl acetate
- filtrationThe mixture was filtered
- customthe filtrate was evaporated
Sources & evidence
- ORD record
- ord-d166baf769d648be8cf6fd344c2ba0c7
- Source dataset
- uspto-grants-2004_11
- Patent number
- US06821965B1
Reaction notes
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