Technology Process of C2H4O2*C27H33Cl3N6O4SSi
There total 7 articles about C2H4O2*C27H33Cl3N6O4SSi which
guide to synthetic route it.
The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:
synthetic route:
- Guidance literature:
-
With
ammonium acetate; ammonia;
In
methanol;
at 70 ℃;
for 24h;
vessel sealed with Teflon screw-cap;
- Guidance literature:
-
With
ammonia;
In
methanol;
at 70 ℃;
for 24h;
Inert atmosphere;
Sealed tube;
DOI:10.1021/jacs.6b02343
- Guidance literature:
-
Multi-step reaction with 6 steps
1.1: 1H-imidazole / N,N-dimethyl-formamide / 14 h / 0 °C / Inert atmosphere
2.1: diisobutylaluminium hydride / dichloromethane; toluene / 2 h / -90 °C / Inert atmosphere
3.1: dichloromethane / 0.33 h / 0 - 20 °C / Inert atmosphere
3.2: 1.67 h / -78 - 20 °C / Inert atmosphere
4.1: 1,3-dimethylbarbituric acid; tetrakis(triphenylphosphine) palladium(0) / dichloromethane / 8 h / Inert atmosphere
4.2: 0.33 h / Inert atmosphere
5.1: 2,4,6-tri-tert-butylpyrimidine / dichloromethane / 29 h / 37 °C / Inert atmosphere; Sealed tube
6.1: ammonia / methanol / 24 h / 70 °C / Inert atmosphere; Sealed tube
With
1H-imidazole; tetrakis(triphenylphosphine) palladium(0); 1,3-dimethylbarbituric acid; ammonia; diisobutylaluminium hydride; 2,4,6-tri-tert-butylpyrimidine;
In
methanol; dichloromethane; N,N-dimethyl-formamide; toluene;
3.1: |Pictet-Spengler Synthesis / 3.2: |Pictet-Spengler Synthesis;
DOI:10.1021/jacs.6b02343