Sodium Hydroxide → HCID 86590693, compound

HRID 1866167Notes

Reaction equation

HRID 1866167 reaction equation
[C:1]([O:5][C:6]([N:8]([CH2:31][C@@H:32]([C:34]1[CH:35]=[N:36][C:37]([Cl:40])=[CH:38][CH:39]=1)[OH:33])[CH2:9][CH2:10][CH2:11][C:12]1[CH:17]=[CH:16][C:15]([C:18]2[CH:23]=[CH:22][C:21]([C:24]([O:26]CC)=[O:25])=[CH:20][C:19]=2[O:29][CH3:30])=[CH:14][CH:13]=1)=[O:7])([CH3:4])([CH3:3])[CH3:2].[OH-].[Na+]>C(O)C.C(OCC)(=O)C.Cl>[C:1]([O:5][C:6]([N:8]([CH2:31][C@@H:32]([C:34]1[CH:35]=[N:36][C:37]([Cl:40])=[CH:38][CH:39]=1)[OH:33])[CH2:9][CH2:10][CH2:11][C:12]1[CH:13]=[CH:14][C:15]([C:18]2[CH:23]=[CH:22][C:21]([C:24]([OH:26])=[O:25])=[CH:20][C:19]=2[O:29][CH3:30])=[CH:16][CH:17]=1)=[O:7])([CH3:4])([CH3:2])[CH3:3]

Participants

6

Procedure

To a solution of ethyl 4′-[3-[(tert-butoxycarbonyl)-[(2R)-2-(6-chloro-3-pyridyl)-2-hydroxyethyl]amino]propyl]-2-methoxy-1,1′-biphenyl-4-carboxylate in ethanol (5.0 ml) was added 1N sodium hydroxide (1.0 ml) and the mixture was stirred for 2 hours at room temperature. The mixture was diluted with ethyl acetate and 1N hydrochloric acid. The organic layer was separated, washed with brine, dried over magnesium sulfate and evaporated. The residue was purified by column chromatography on silica gel (hexane/ethyl acetate=1/1) to give 4′-[3-[(tert-butoxycarbonyl)[(2R)-2-(6-chloro-3-pyridyl)-2-hydroxyethyl]amino]propyl]-2-methoxy-1,1′-biphenyl-4-carboxylic acid (100 mg).

Workup

  1. customThe organic layer was separated
  2. washwashed with brine
  3. dry with materialdried over magnesium sulfate
  4. customevaporated
  5. customThe residue was purified by column chromatography on silica gel (hexane/ethyl acetate=1/1)

Sources & evidence

ORD record
ord-d8c97a2ef6b44c3aa309766f2fe8d1c3
Source dataset
uspto-grants-2009_12
Patent number
US07629366B2

Reaction notes

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