Sodium Hydroxide → Sodium Nalpha-[3-(3-Hydroxyphenyl)acryloyl]-L-Tryptophanate
Reaction equation
C([O:4][C:5]1[CH:6]=[C:7]([CH:11]=[CH:12][C:13]([NH:15][C@H:16]([C:27]([O:29]C)=[O:28])[CH2:17][C:18]2[C:26]3[C:21](=[CH:22][CH:23]=[CH:24][CH:25]=3)[NH:20][CH:19]=2)=[O:14])[CH:8]=[CH:9][CH:10]=1)(=O)C.[OH-].[Na+:32]>CO>[OH:4][C:5]1[CH:6]=[C:7]([CH:11]=[CH:12][C:13]([NH:15][C@H:16]([C:27]([O-:29])=[O:28])[CH2:17][C:18]2[C:26]3[C:21](=[CH:22][CH:23]=[CH:24][CH:25]=3)[NH:20][CH:19]=2)=[O:14])[CH:8]=[CH:9][CH:10]=1.[Na+:32]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
The same procedures as in Example 60 were carried out from the compound obtained in Example 3 (4.7 g), 1 mol/L of an aqueous sodium hydroxide solution (35 mL), and methanol (300 mL), to give the captioned compound (2.8 g, 65%) as crystals.
Sources & evidence
- ORD record
- ord-86013e9fd7d84460ae0a357bd79395b2
- Source dataset
- uspto-grants-2015_10
- Patent number
- US09150510B2
Reaction notes
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