Lithium Hydroxide → 6-[[1-Phenyl-2-propylmercapto-1H-benzimidazol-6-yl]oxy]Hexanoic Acid

HRID 1070874Notes

Reaction equation

HRID 1070874 reaction equation
C[O:2][C:3](=[O:29])[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][CH:25]=[CH:24][CH:23]=3)[C:14]=2[CH:28]=1.[OH-].[Li+]>>[C:22]1([N:15]2[C:14]3[CH:28]=[C:10]([O:9][CH2:8][CH2:7][CH2:6][CH2:5][CH2:4][C:3]([OH:29])=[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][CH:25]=[CH:26][CH:27]=1

Participants

3

Reactant 2

HCID 3939Lithium HydroxideHCID 102234206-[[1-phenyl-2-propylmercapto-1H-benzimidazol-6-yl]oxy]hexanoic acid methyl ester

Product 1

HCID 102722066-[[1-Phenyl-2-propylmercapto-1H-benzimidazol-6-yl]oxy]Hexanoic Acid

Procedure

109 mg of 6-[[1-phenyl-2-propylmercapto-1H-benzimidazol-6-yl]oxy]hexanoic acid methyl ester was reacted according to general operating instructions 3 with lithium hydroxide. 104 mg was obtained.

Workup

  1. custom104 mg was obtained

Sources & evidence

ORD record
ord-d6970d593c664fbcb4adb42377779d1b
Source dataset
uspto-grants-2005_06
Patent number
US06903126B2

Reaction notes

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