Technology Process of methyl 2-(((benzyloxy)carbonyl)amino)-1-methyl-1H-indole-3-carboxylate
There total 6 articles about methyl 2-(((benzyloxy)carbonyl)amino)-1-methyl-1H-indole-3-carboxylate which
guide to synthetic route it.
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synthetic route:
- Guidance literature:
-
3-(methoxycarbonyl)-1-methyl-1H-indole-2-carboxylic acid;
With
diphenyl phosphoryl azide; triethylamine;
In
N,N-dimethyl-formamide;
at 20 ℃;
for 2h;
under 760.051 Torr;
Cooling with ice;
benzyl alcohol;
In
N,N-dimethyl-formamide;
at 80 ℃;
for 3h;
under 760.051 Torr;
- Guidance literature:
-
Multi-step reaction with 6 steps
1.1: oxygen; palladium diacetate; acetic acid / N,N-dimethyl acetamide / 18 h / 115 °C / 760.05 Torr
2.1: sodium hydride / 8 h / 0 - 75 °C / 760.05 Torr
3.1: potassium hydroxide / ethanol / 8 h / 760.05 Torr / Reflux
4.1: trifluoroacetic anhydride / dichloromethane / 2 h / 760.05 Torr
5.1: trifluoroacetic anhydride / 18 h / 20 °C / 760.05 Torr
6.1: triethylamine; diphenyl phosphoryl azide / N,N-dimethyl-formamide / 2 h / 20 °C / 760.05 Torr / Cooling with ice
6.2: 3 h / 80 °C / 760.05 Torr
With
diphenyl phosphoryl azide; oxygen; palladium diacetate; sodium hydride; acetic acid; triethylamine; trifluoroacetic anhydride; potassium hydroxide;
In
ethanol; dichloromethane; N,N-dimethyl acetamide; N,N-dimethyl-formamide;
- Guidance literature:
-
Multi-step reaction with 5 steps
1.1: sodium hydride / 8 h / 0 - 75 °C / 760.05 Torr
2.1: potassium hydroxide / ethanol / 8 h / 760.05 Torr / Reflux
3.1: trifluoroacetic anhydride / dichloromethane / 2 h / 760.05 Torr
4.1: trifluoroacetic anhydride / 18 h / 20 °C / 760.05 Torr
5.1: triethylamine; diphenyl phosphoryl azide / N,N-dimethyl-formamide / 2 h / 20 °C / 760.05 Torr / Cooling with ice
5.2: 3 h / 80 °C / 760.05 Torr
With
diphenyl phosphoryl azide; sodium hydride; triethylamine; trifluoroacetic anhydride; potassium hydroxide;
In
ethanol; dichloromethane; N,N-dimethyl-formamide;