Oxalic Acid → HCID 178422762, compound
Reaction equation
[Cl:1][C:2]1[CH:7]=[CH:6][CH:5]=[C:4]([F:8])[C:3]=1[NH:9][C:10]1[NH:11][C:12]2[C:18]3[CH2:19][C:20]([CH3:23])([CH3:22])[O:21][C:17]=3[C:16]([C:24]([NH:26][C:27]3[CH:32]=[CH:31][C:30]([C:33]([F:36])([F:35])[F:34])=[CH:29][CH:28]=3)=[O:25])=[CH:15][C:13]=2[N:14]=1.[C:37]([OH:42])(=[O:41])[C:38]([OH:40])=[O:39]>CC(C)=O>[C:37]([OH:42])(=[O:41])[C:38]([OH:40])=[O:39].[Cl:1][C:2]1[CH:7]=[CH:6][CH:5]=[C:4]([F:8])[C:3]=1[NH:9][C:10]1[NH:11][C:12]2[C:18]3[CH2:19][C:20]([CH3:22])([CH3:23])[O:21][C:17]=3[C:16]([C:24]([NH:26][C:27]3[CH:28]=[CH:29][C:30]([C:33]([F:35])([F:36])[F:34])=[CH:31][CH:32]=3)=[O:25])=[CH:15][C:13]=2[N:14]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
To a solution of 2-[(2-chloro-6-fluorophenyl)amino]-7,7-dimethyl-N-[4-(trifluoromethyl)phenyl]-7,8-dihydro-1H-furo[3,2-e]benzimidazole-5-carboxamide (Example-107, 0.100 g) in acetone was added oxalic acid. The reaction mass was refluxed for 3 h. The reaction mass was filtered. The obtained residue was washed with pentane and DEE to afford 0.100 g of the desired product.
Workup
- temperatureThe reaction mass was refluxed for 3 h
- filtrationThe reaction mass was filtered
- washThe obtained residue was washed with pentane and DEE
Sources & evidence
- ORD record
- ord-c21b5aa6ea6643e980541b093150aa22
- Source dataset
- uspto-grants-2013_08
- Patent number
- US08519149B2
Reaction notes
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