Lithium Hydroxide → 6-[[1-(4-Methylphenyl)-2-propylmercapto-1H-benzimidazol-6-yl]oxy]Hexanoic Acid

HRID 1070879Notes

Reaction equation

HRID 1070879 reaction equation
C[O:2][C:3](=[O:30])[CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][O:9][C:10]1[CH:11]=[CH:12][C:13]2[N:17]=[C:16]([S:18][CH2:19][CH2:20][CH3:21])[N:15]([C:22]3[CH:27]=[CH:26][C:25]([CH3:28])=[CH:24][CH:23]=3)[C:14]=2[CH:29]=1.[OH-].[Li+]>>[CH3:28][C:25]1[CH:26]=[CH:27][C:22]([N:15]2[C:14]3[CH:29]=[C:10]([O:9][CH2:8][CH2:7][CH2:6][CH2:5][CH2:4][C:3]([OH:30])=[O:2])[CH:11]=[CH:12][C:13]=3[N:17]=[C:16]2[S:18][CH2:19][CH2:20][CH3:21])=[CH:23][CH:24]=1

Participants

3

Reactant 2

HCID 3939Lithium HydroxideHCID 102960776-[[1-(4-Methylphenyl)-2-propylmercapto-1H-benzimidazol-6-yl]oxy]Hexanoic Acid Methyl Ester

Product 1

HCID 694330506-[[1-(4-Methylphenyl)-2-propylmercapto-1H-benzimidazol-6-yl]oxy]Hexanoic Acid

Procedure

128 mg of 6-[[1-(4-methylphenyl)-2-propylmercapto-1H-benzimidazol-6-yl]oxy]-hexanoic acid methyl ester was reacted with lithium hydroxide according to general operating instructions 3. 98 mg was obtained.

Workup

  1. custom98 mg was obtained

Sources & evidence

ORD record
ord-5c8b40c2b0544d028933b63658d2a488
Source dataset
uspto-grants-2005_06
Patent number
US06903126B2

Reaction notes

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