Citric Acid → HCID 178463789, compound
Reaction equation
C[O:2][C:3](=[O:37])[C:4]1[CH:9]=[CH:8][CH:7]=[C:6]([NH:10][C:11]2[NH:15][C:14]3[CH:16]=[C:17]([N:32]([CH2:35][CH3:36])[CH2:33][CH3:34])[C:18]([C:20](=[O:31])[NH:21][C:22]4[CH:30]=[C:29]5[C:25]([CH:26]=[N:27][NH:28]5)=[CH:24][CH:23]=4)=[CH:19][C:13]=3[N:12]=2)[CH:5]=1.[Li+].[OH-].C(O)(=O)CC(CC(O)=O)(C(O)=O)O>CO.C1COCC1>[CH2:35]([N:32]([CH2:33][CH3:34])[C:17]1[C:18]([C:20](=[O:31])[NH:21][C:22]2[CH:30]=[C:29]3[C:25]([CH:26]=[N:27][NH:28]3)=[CH:24][CH:23]=2)=[CH:19][C:13]2[N:12]=[C:11]([NH:10][C:6]3[CH:5]=[C:4]([CH:9]=[CH:8][CH:7]=3)[C:3]([OH:37])=[O:2])[NH:15][C:14]=2[CH:16]=1)[CH3:36]Participants
6
Reactant 3
Product 1
Reagents, catalysts & solvents 2
Procedure
To a solution of 3-[6-diethylamino-5-(1H-indazol-6-ylcarbamoyl)-1H-benzimidazol-2-ylamino]-benzoic acid methyl ester (0.2 mmol; see Example 115) in methanol (2 mL) and THF (2 mL) was added 1M aqueous LiOH solution (2 mL). The resulting solution was then stirred at RT until the reaction was complete. The pH of the reaction mixture was adjusted with 5% aqueous citric acid solution to bring its pH to 4-5. The solid obtained was filtered, washed with ice-cold water, and dried under vacuum to afford 3-[6-diethylamino-5-(1H-indazol-6-ylcarbamoyl)-1H-benzimidazol-2-ylamino]-benzoic acid as a white solid. MS: m/z 484 (M+H)+.
Workup
- customThe solid obtained
- filtrationwas filtered
- washwashed with ice-cold water
- customdried under vacuum
Sources & evidence
- ORD record
- ord-1844ff76f7624186b903ce84f5c1df68
- Source dataset
- uspto-grants-2010_10
- Patent number
- US07820821B2
Reaction notes
Loading…