Technology Process of C28H35N5O2
There total 3 articles about C28H35N5O2 which
guide to synthetic route it.
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synthetic route:
- Guidance literature:
-
With
copper(l) chloride; tris[(1-benzyl-1H-1,2,3-triazol-4yl)methyl]amine;
In
dichloromethane;
at 20 ℃;
for 20h;
Inert atmosphere;
Schlenk technique;
Sealed tube;
DOI:10.1039/c4gc00031e
- Guidance literature:
-
Multi-step reaction with 4 steps
1: 24 h / 20 °C / Inert atmosphere
2: toluene-4-sulfonic acid / methanol / 24 h / Reflux
3: potassium carbonate / acetonitrile; toluene / 0 - 20 °C / Inert atmosphere
4: copper(l) chloride; tris[(1-benzyl-1H-1,2,3-triazol-4yl)methyl]amine / dichloromethane / 20 h / 20 °C / Inert atmosphere; Schlenk technique; Sealed tube
With
potassium carbonate; toluene-4-sulfonic acid; copper(l) chloride; tris[(1-benzyl-1H-1,2,3-triazol-4yl)methyl]amine;
In
methanol; dichloromethane; toluene; acetonitrile;
DOI:10.1039/c4gc00031e
- Guidance literature:
-
Multi-step reaction with 3 steps
1: toluene-4-sulfonic acid / methanol / 24 h / Reflux
2: potassium carbonate / acetonitrile; toluene / 0 - 20 °C / Inert atmosphere
3: copper(l) chloride; tris[(1-benzyl-1H-1,2,3-triazol-4yl)methyl]amine / dichloromethane / 20 h / 20 °C / Inert atmosphere; Schlenk technique; Sealed tube
With
potassium carbonate; toluene-4-sulfonic acid; copper(l) chloride; tris[(1-benzyl-1H-1,2,3-triazol-4yl)methyl]amine;
In
methanol; dichloromethane; toluene; acetonitrile;
DOI:10.1039/c4gc00031e
![(5S)-3-butyl-2,2-dimethyl-5-{[4-(prop-2-yn-1-yloxy)phenyl]methyl}imidazolidin-4-one](/Databaselist/images/loading.webp)
