Sodium Hydroxide → 2-Butoxy-2-methyl-3-(4-{2-[3-methyl-2-oxo-1-(3-trifluoromethyl-benzyl)-imidazolidin-4-yl]-ethoxy}-phenyl)-propionic acid

HRID 1985157Notes

Reaction equation

HRID 1985157 reaction equation
C([O:3][C:4](=[O:40])[C:5]([O:35][CH2:36][CH2:37][CH2:38][CH3:39])([CH3:34])[CH2:6][C:7]1[CH:12]=[CH:11][C:10]([O:13][CH2:14][CH2:15][CH:16]2[CH2:20][N:19]([CH2:21][C:22]3[CH:27]=[CH:26][CH:25]=[C:24]([C:28]([F:31])([F:30])[F:29])[CH:23]=3)[C:18](=[O:32])[N:17]2[CH3:33])=[CH:9][CH:8]=1)C.[OH-].[Na+]>C(O)C>[CH2:36]([O:35][C:5]([CH3:34])([CH2:6][C:7]1[CH:8]=[CH:9][C:10]([O:13][CH2:14][CH2:15][CH:16]2[CH2:20][N:19]([CH2:21][C:22]3[CH:27]=[CH:26][CH:25]=[C:24]([C:28]([F:31])([F:29])[F:30])[CH:23]=3)[C:18](=[O:32])[N:17]2[CH3:33])=[CH:11][CH:12]=1)[C:4]([OH:40])=[O:3])[CH2:37][CH2:38][CH3:39]

Participants

4

Reactant 2

HCID 14798Sodium HydroxideHCID 688684932-Butoxy-2-methyl-3-(4-{2-[3-methyl-2-oxo-1-(3-trifluoromethyl-benzyl)-imidazolidin-4-yl]-ethoxy}-phenyl)-propionic acid ethyl ester

Product 1

HCID 102181972-Butoxy-2-methyl-3-(4-{2-[3-methyl-2-oxo-1-(3-trifluoromethyl-benzyl)-imidazolidin-4-yl]-ethoxy}-phenyl)-propionic acid

Reagents, catalysts & solvents 1

HCID 702EthanolSolvent

Procedure

A solution of 2-Butoxy-2-methyl-3-(4-{2-[3-methyl-2-oxo-1-(3-trifluoromethyl-benzyl)-imidazolidin-4-yl]-ethoxy}-phenyl)-propionic acid ethyl ester and 5N NaOH (0.3 mL) in ethanol (3 mL) is refluxed under nitrogen for 1 h, cooled to ambient temperature, and concentrated. The residue is diluted with 1N HCl, extracted with CH2Cl2, dried, concentrated, and purified by LCMS to provide the title compound. 1H NMR (400 MHz, CDCl3): δ 7.51-7.38 (m, 4H), 7.04 (d, 2H, J=8.8 Hz), 6.69 (d, 2H, J=8.8 Hz), 4.46, 4.34 (ABq, 2H, J=14.9 Hz), 3.94 (t, 2H, J=5.7 Hz), 3.68-3.60 (m, 1H), 3.57-3.52 (m, 1H), 3.48-3.43 (m, 1H), 3.38 (t, 1H, J=8.8 Hz), 2.98, 2.92 (ABq, 2H, J=14.4 Hz), 2.83 (s, 3H), 2.25-2.18 (m, 1H), 1.91-1.83 (m, 1H), 1.59-1.52 (m, 2H), 1.45 (s, 3H), 1.39-1.30 (m, 2H), 0.91 (t, 3H, J=7.2 Hz). MS [EI+] 537 (M+H)+, [EI−] 535 (M−H)+.

Workup

  1. concentrationconcentrated
  2. additionThe residue is diluted with 1N HCl
  3. extractionextracted with CH2Cl2
  4. customdried
  5. concentrationconcentrated
  6. custompurified by LCMS

Sources & evidence

ORD record
ord-14bb834466b34e24858c2153aa51c203
Source dataset
uspto-grants-2009_06
Patent number
US07544812B2

Reaction notes

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