Lithium Hydroxide → HCID 21310525, compound

HRID 583419Notes

Reaction equation

HRID 583419 reaction equation
C([O:3][C:4](=[O:36])[CH2:5][CH2:6][CH:7]([N:18]([CH3:35])[C:19](=[O:34])[C:20]1[CH:25]=[C:24]([C:26]([F:29])([F:28])[F:27])[CH:23]=[C:22]([C:30]([F:33])([F:32])[F:31])[CH:21]=1)[CH2:8][C:9]1[C:17]2[C:12](=[CH:13][CH:14]=[CH:15][CH:16]=2)[NH:11][CH:10]=1)C.[OH-].[Li+]>O1CCCC1.CO.O>[CH3:35][N:18]([CH:7]([CH2:8][C:9]1[C:17]2[C:12](=[CH:13][CH:14]=[CH:15][CH:16]=2)[NH:11][CH:10]=1)[CH2:6][CH2:5][C:4]([OH:36])=[O:3])[C:19](=[O:34])[C:20]1[CH:21]=[C:22]([C:30]([F:33])([F:32])[F:31])[CH:23]=[C:24]([C:26]([F:29])([F:28])[F:27])[CH:25]=1

Participants

4

Procedure

A solution of 30 g of 4-[N-methyl-N-(3,5-bistrifluoromethyl-benzoyl)-amino]-5-(1H-indol-3-yl)-pentanoic acid ethyl ester and 3.7 g of lithium hydroxide in 210 ml of tetrahydrofuran/methanol/water=2/2/1 is stirred at room temperature for 3 hours and then concentrated by evaporation. The residue is dissolved in 300 ml of water, extracted with ether, acidified to pH=2 with 0.1N hydrochloric acid and extracted three times with ether. The combined organic phases originating from the extraction of the acidic aqueous phase are washed with water and saturated NaCl solution, dried (magnesium sulfate) and concentrated by evaporation. In this way the title compound is obtained in the form of a yellow foam.

Workup

  1. concentrationconcentrated by evaporation
  2. dissolutionThe residue is dissolved in 300 ml of water
  3. extractionextracted with ether
  4. extractionextracted three times with ether
  5. extractionThe combined organic phases originating from the extraction of the acidic aqueous phase
  6. washare washed with water and saturated NaCl solution
  7. dry with materialdried (magnesium sulfate)
  8. concentrationconcentrated by evaporation

Sources & evidence

ORD record
ord-e685e5c2ddf54f27aeaf391e5fa2bd73
Source dataset
uspto-grants-1999_07
Patent number
US05929067

Reaction notes

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