Lithium Hydroxide → HCID 25125216, compound

HRID 1747451Notes

Reaction equation

HRID 1747451 reaction equation
C([O:3][C:4](=[O:32])[CH2:5][CH:6]([N:10]1[C:14]2[CH:15]=[CH:16][CH:17]=[CH:18][C:13]=2[N:12]([CH2:19][C:20]2[CH:21]=[C:22]([Br:30])[CH:23]=[C:24]3[C:28]=2[N:27]([CH3:29])[CH:26]=[CH:25]3)[C:11]1=[O:31])[CH2:7][CH2:8][CH3:9])C.[Li+].[OH-]>O1CCOCC1.O>[Br:30][C:22]1[CH:23]=[C:24]2[C:28](=[C:20]([CH2:19][N:12]3[C:13]4[CH:18]=[CH:17][CH:16]=[CH:15][C:14]=4[N:10]([CH:6]([CH2:7][CH2:8][CH3:9])[CH2:5][C:4]([OH:32])=[O:3])[C:11]3=[O:31])[CH:21]=1)[N:27]([CH3:29])[CH:26]=[CH:25]2

Participants

5

Reactant 2

HCID 3939Lithium HydroxideHCID 594976003-[3-(5-Bromo-1-methyl-1H-indol-7-ylmethyl)-2-oxo-2,3-dihydro-benzimidazol-1-yl]-hexanoic acid ethyl ester

Product 1

HCID 25125216HCID 25125216, compound

Reagents, catalysts & solvents 2

HCID 962WaterSolventHCID 312751,4-DioxaneSolvent

Procedure

To a solution of 3-[3-(5-Bromo-1-methyl-1H-indol-7-ylmethyl)-2-oxo-2,3-dihydro-benzimidazol-1-yl]-hexanoic acid ethyl ester (10 mg, 0.02 mmol) in 1,4-dioxane (5 mL) and water (1 mL) was added LiOH (1 mg, 0.04 mmol) at room temperature. The solution was stirred at the same temperature for 4 hours. The solution was concentrated and water was added to the residue. The solution was acidified by 12N HCl in an ice-bath. The solid that preciptate out from the solution was collected by filtration. The solid was dried under vacuum and was confirmed to be the desirable product. LCMS (ESMS): m/z 471.17 (M+H+).

Workup

  1. concentrationThe solution was concentrated
  2. additionwater was added to the residue
  3. customThe solution was acidified by 12N HCl in an ice-bath
  4. filtrationThe solid that preciptate out from the solution was collected by filtration
  5. customThe solid was dried under vacuum

Sources & evidence

ORD record
ord-95a17401408744389594fda835723454
Source dataset
uspto-grants-2015_10
Patent number
US09150556B2

Reaction notes

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