Technology Process of C32H44N4O10
There total 10 articles about C32H44N4O10 which
guide to synthetic route it.
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synthetic route:
- Guidance literature:
-
N-(tert-butoxycarbonyl)-L-alanyl-L-alanyl-L-phenylalanine;
With
benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride;
In
dichloromethane;
at 0 ℃;
for 0.25h;
Inert atmosphere;
C12H17NO5;
With
N-ethyl-N,N-diisopropylamine;
In
dichloromethane;
at 0 - 20 ℃;
for 8h;
Inert atmosphere;
DOI:10.1021/ol5002126
- Guidance literature:
-
Multi-step reaction with 2 steps
1.1: lithium hydroxide / water; tetrahydrofuran; methanol / 1 h / 0 - 20 °C / Inert atmosphere
2.1: benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / dichloromethane / 0.25 h / 0 °C / Inert atmosphere
2.2: 8 h / 0 - 20 °C / Inert atmosphere
With
benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; lithium hydroxide;
In
tetrahydrofuran; methanol; dichloromethane; water;
DOI:10.1021/ol5002126
- Guidance literature:
-
Multi-step reaction with 4 steps
1.1: N-Bromosuccinimide; 2,2'-azobis(isobutyronitrile) / tetrachloromethane / 2 h / Inert atmosphere; Reflux
2.1: sodium azide / N,N-dimethyl-formamide / 0.5 h / 65 °C / Inert atmosphere
3.1: hydrogen; palladium on activated charcoal / ethyl acetate / 1 h / 760.05 Torr
4.1: benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / dichloromethane / 0.25 h / 0 °C / Inert atmosphere
4.2: 8 h / 0 - 20 °C / Inert atmosphere
With
N-Bromosuccinimide; sodium azide; 2,2'-azobis(isobutyronitrile); palladium on activated charcoal; hydrogen; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride;
In
tetrachloromethane; dichloromethane; ethyl acetate; N,N-dimethyl-formamide;
DOI:10.1021/ol5002126