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Water → (S)-2-(2-(3,5-dimethylphenyl)acetamido)-3-(1H-indol-3-yl)propionic acid

HRID 71026
Notes
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Reaction equation

HRID 71026 reaction equation
[Li+].[OH-].[CH3:3][C:4]1[CH:5]=[C:6]([CH2:11][C:12]([NH:14][C@@H:15]([CH2:20][C:21]2[C:29]3[C:24](=[CH:25][CH:26]=[CH:27][CH:28]=3)[NH:23][CH:22]=2)[C:16]([O:18]C)=[O:17])=[O:13])[CH:7]=[C:8]([CH3:10])[CH:9]=1.O>CO>[CH3:10][C:8]1[CH:7]=[C:6]([CH2:11][C:12]([NH:14][C@@H:15]([CH2:20][C:21]2[C:29]3[C:24](=[CH:25][CH:26]=[CH:27][CH:28]=3)[NH:23][CH:22]=2)[C:16]([OH:18])=[O:17])=[O:13])[CH:5]=[C:4]([CH3:3])[CH:9]=1
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

5

Reactant 3

HCID 962WaterHCID 3939Lithium HydroxideHCID 67042226(S)-methyl 2-(2-(3,5-dimethylphenyl)acetamido)-3-(1H-indol-3-yl)propanoate

Product 1

HCID 67041847(S)-2-(2-(3,5-dimethylphenyl)acetamido)-3-(1H-indol-3-yl)propionic acidYield 93%

Reagents, catalysts & solvents 1

HCID 887MethanolSolvent

Procedure

DMAP (122.2 mg, 0.5 mmol) and DIC (N,N-diisopropylcarbodiimide) (235 μl, 1.5 mmol) were added to a solution of tryptophan methyl ester (255 mg, 1.0 mmol) and 3,5-dimethylphenylacetic acid (164 mg, 1.0 mmol) in dry DCM (11 ml). After 17 h at room temperature the solvent was removed under reduced pressure and the crude product was purified by flash chromatography (DCM containing 1% EtOH) to afford (S)-methyl 2-(2-(3,5-dimethylphenyl)acetamido)-3-(1H-indol-3-yl)propanoate. An aqueous solution of LiOH (1N, 4.5 ml, 4.5 mmol) was added to a solution of (S)-methyl 2-(2-(3,5-dimethylphenyl)acetamido)-3-(1H-indol-3-yl)propanoate (365 mg, 1 mmol) in methanol (24.5 ml) and the reaction mixture was stirred at room temperature for 4.5 h. Then water was added and methanol was removed under reduced pressure. The aqueous residue was washed with DCM (5×20 ml), treated with HCl 2N to obtain a pH 4 and extracted with DCM (3×25 ml). The organic phases were dried with anhydrous Na2SO4 and the solvent was removed under reduced pressure to afford (S)-2-(2-(3,5-dimethylphenyl)acetamido)-3-(1H-indol-3-yl)propionic acid (93% c.y.).

Workup

  1. custommethanol was removed under reduced pressure
  2. washThe aqueous residue was washed with DCM (5×20 ml)
  3. additiontreated with HCl 2N
  4. customto obtain a pH 4
  5. extractionextracted with DCM (3×25 ml)
  6. dry with materialThe organic phases were dried with anhydrous Na2SO4
  7. customthe solvent was removed under reduced pressure

Sources & evidence

ORD record
ord-aec14985f9e44d918aee656434653173
Source dataset
uspto-grants-2014_09
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US08822698B2

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes