HCID 2805345, Verbindung → HCID 10269970, Verbindung
Reaktionsgleichung
[CH2:1]([O:3][C:4]([C:6]1[N:7]([CH3:13])[C:8](Br)=[N:9][C:10]=1[CH3:11])=[O:5])[CH3:2].[C:14]([C:16]1[CH:17]=[C:18]([N:22]2[C:26]([CH3:27])=[CH:25][CH:24]=[C:23]2[CH3:28])[CH:19]=[CH:20][CH:21]=1)#[CH:15]>>[CH2:1]([O:3][C:4]([C:6]1[N:7]([CH3:13])[C:8]([C:15]#[C:14][C:16]2[CH:21]=[CH:20][CH:19]=[C:18]([N:22]3[C:26]([CH3:27])=[CH:25][CH:24]=[C:23]3[CH3:28])[CH:17]=2)=[N:9][C:10]=1[CH3:11])=[O:5])[CH3:2]Komponenten
3
Versuchsvorschrift
The title compound, MS: m/e=362.8 (M+H+), was prepared in accordance with the general method of example 1b from 2-bromo-3,5-dimethyl-3H-imidazole-4-carboxylic acid ethyl ester and 1-(3-ethynyl-phenyl)-2,5-dimethyl-1H-pyrrole.
Quellen und Nachweise
- ORD-Eintrag
- ord-a143ec2df361457a84c618be1f8a5872
- Quelldatensatz
- uspto-grants-2005_12
- Patentnummer
- US06972299B2