Citric Acid → HCID 178463789, compound

HRID 1163442Notes

Reaction equation

HRID 1163442 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

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

  1. customThe solid obtained
  2. filtrationwas filtered
  3. washwashed with ice-cold water
  4. customdried under vacuum

Sources & evidence

ORD record
ord-1844ff76f7624186b903ce84f5c1df68
Source dataset
uspto-grants-2010_10
Patent number
US07820821B2

Reaction notes

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