Technology Process of C29H33F2N3O6
There total 13 articles about C29H33F2N3O6 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:
-
Multi-step reaction with 9 steps
1: triphenylphosphine; di-isopropyl azodicarboxylate / tetrahydrofuran / 7 h / Reflux
2: hydrogen; 10 wt% Pd(OH)2 on carbon / methanol / 22 h
3: Rh/Al2O3; trifluoroacetic acid; hydrogen / methanol / 15 h / 10?atm
4: sodium hydrogencarbonate / acetonitrile; water / 48 h / 20 °C
5: sodium ethanolate / ethanol / 16 h / Inert atmosphere; Reflux
6: potassium carbonate / 2 h / 60 °C
7: trifluoroacetic acid / dichloromethane / 1 h / 20 °C
8: triethylamine; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; benzotriazol-1-ol / N,N-dimethyl-formamide / 2 h / 20 °C
9: water; sodium hydroxide / tetrahydrofuran / 20 h / 20 °C
With
di-isopropyl azodicarboxylate; 10 wt% Pd(OH)2 on carbon; Rh/Al2O3; water; hydrogen; sodium ethanolate; sodium hydrogencarbonate; potassium carbonate; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; triphenylphosphine; trifluoroacetic acid; sodium hydroxide;
In
tetrahydrofuran; methanol; ethanol; dichloromethane; water; N,N-dimethyl-formamide; acetonitrile;
1: |Mitsunobu Displacement;
DOI:10.1016/j.bmc.2012.11.003
- Guidance literature:
-
Multi-step reaction with 9 steps
1: triphenylphosphine; di-isopropyl azodicarboxylate / tetrahydrofuran / 7 h / Reflux
2: hydrogen; 10 wt% Pd(OH)2 on carbon / methanol / 22 h
3: Rh/Al2O3; trifluoroacetic acid; hydrogen / methanol / 15 h / 10?atm
4: sodium hydrogencarbonate / acetonitrile; water / 48 h / 20 °C
5: sodium ethanolate / ethanol / 16 h / Inert atmosphere; Reflux
6: potassium carbonate / 2 h / 60 °C
7: trifluoroacetic acid / dichloromethane / 1 h / 20 °C
8: triethylamine; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; benzotriazol-1-ol / N,N-dimethyl-formamide / 2 h / 20 °C
9: water; sodium hydroxide / tetrahydrofuran / 20 h / 20 °C
With
di-isopropyl azodicarboxylate; 10 wt% Pd(OH)2 on carbon; Rh/Al2O3; water; hydrogen; sodium ethanolate; sodium hydrogencarbonate; potassium carbonate; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; triphenylphosphine; trifluoroacetic acid; sodium hydroxide;
In
tetrahydrofuran; methanol; ethanol; dichloromethane; water; N,N-dimethyl-formamide; acetonitrile;
1: |Mitsunobu Displacement;
DOI:10.1016/j.bmc.2012.11.003
- Guidance literature:
-
Multi-step reaction with 7 steps
1: Rh/Al2O3; trifluoroacetic acid; hydrogen / methanol / 15 h / 10?atm
2: sodium hydrogencarbonate / acetonitrile; water / 48 h / 20 °C
3: sodium ethanolate / ethanol / 16 h / Inert atmosphere; Reflux
4: potassium carbonate / 2 h / 60 °C
5: trifluoroacetic acid / dichloromethane / 1 h / 20 °C
6: triethylamine; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; benzotriazol-1-ol / N,N-dimethyl-formamide / 2 h / 20 °C
7: water; sodium hydroxide / tetrahydrofuran / 20 h / 20 °C
With
Rh/Al2O3; water; hydrogen; sodium ethanolate; sodium hydrogencarbonate; potassium carbonate; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; trifluoroacetic acid; sodium hydroxide;
In
tetrahydrofuran; methanol; ethanol; dichloromethane; water; N,N-dimethyl-formamide; acetonitrile;
DOI:10.1016/j.bmc.2012.11.003