1-Bromopropane → HCID 54547184, Verbindung

Reaktionsgleichung

[CH2:1]([O:3][C:4](=[O:25])[C:5]([CH3:24])([O:7][C:8]1[CH:16]=[CH:15][CH:14]=[C:13]2[C:9]=1[C:10]([C:18]1[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=1)=[C:11]([CH3:17])[NH:12]2)[CH3:6])[CH3:2].[CH2:26](Br)[CH2:27][CH3:28]>>[CH2:1]([O:3][C:4](=[O:25])[C:5]([CH3:24])([O:7][C:8]1[CH:16]=[CH:15][CH:14]=[C:13]2[C:9]=1[C:10]([C:18]1[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=1)=[C:11]([CH3:17])[N:12]2[CH2:26][CH2:27][CH3:28])[CH3:6])[CH3:2]

Komponenten

Edukt 2

HCID 78401-Bromopropane

HCID 538412442-Methyl-2-[2-methyl-3-phenyl-1H-indole-4-yloxy]-propanoic acid ethylester

Produkt 1

HCID 54547184HCID 54547184, Verbindung

Versuchsvorschrift

The above compound was prepared from 2-methyl-2-[2-methyl-3-phenyl-1H-indole-4-yloxy]-propanoic acid ethylester and propylbromide using a procedure analogous to that of Example 63.

Quellen und Nachweise

ORD-Eintrag: ord-508bf23e577b4350af5f2931d03eb76b
Quelldatensatz: uspto-grants-1982_08
DOI: 10.6084/m9.figshare.5104873.v1
Patentnummer: US04343811

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