Sodium Hydroxide → N-[3-(3-Fluorophenyl)acryloyl]-O4-Methyl-L-Tyrosine
Reaktionsgleichung
[F:1][C:2]1[CH:3]=[C:4]([CH:8]=[CH:9][C:10]([NH:12][C@H:13]([C:23]([O:25]C)=[O:24])[CH2:14][C:15]2[CH:20]=[CH:19][C:18]([O:21][CH3:22])=[CH:17][CH:16]=2)=[O:11])[CH:5]=[CH:6][CH:7]=1.[OH-].[Na+]>CO>[F:1][C:2]1[CH:3]=[C:4]([CH:8]=[CH:9][C:10]([NH:12][C@H:13]([C:23]([OH:25])=[O:24])[CH2:14][C:15]2[CH:16]=[CH:17][C:18]([O:21][CH3:22])=[CH:19][CH:20]=2)=[O:11])[CH:5]=[CH:6][CH:7]=1Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
The same procedures as in Example 90 were carried out from the compound obtained in Example 39 (2.9 g), 1 mol/L of an aqueous sodium hydroxide solution (12 mL), and methanol (120 mL), to give the captioned compound (1.7 g, 61%) as crystals.
Quellen und Nachweise
- ORD-Eintrag
- ord-ce41083ae6934bd2bcef96867a2c0188
- Quelldatensatz
- uspto-grants-2015_10
- Patentnummer
- US09150510B2
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