Technology Process of C25H29F6N3O2
There total 4 articles about C25H29F6N3O2 which
guide to synthetic route it.
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synthetic route:
- Guidance literature:
-
Multi-step reaction with 6 steps
1.1: (1S)-10-camphorsulfonic acid / toluene / 0.5 h / Reflux; Inert atmosphere
1.2: 3 h / 20 °C / Inert atmosphere
2.1: 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; dmap / dichloromethane / 18 h / 20 °C / Inert atmosphere
3.1: hydrogen; 10% palladium hydroxide on charcoal / methanol / 16 h / 20 °C / 760.05 Torr / Inert atmosphere
4.1: dichloromethane / 18 h / 20 °C / Inert atmosphere
4.2: 20 h / 20 °C / Inert atmosphere
5.1: 3-[(diethoxyphosphinyl)oxy]-1,2,3-benzotriazin-4(3H)-one; N-ethyl-N,N-diisopropylamine / dichloromethane / 18 h / 20 °C / Inert atmosphere
6.1: hydrogenchloride / 1,4-dioxane / 48 h / 20 °C / Inert atmosphere
With
hydrogenchloride; dmap; 10% palladium hydroxide on charcoal; (1S)-10-camphorsulfonic acid; hydrogen; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine; 3-[(diethoxyphosphinyl)oxy]-1,2,3-benzotriazin-4(3H)-one;
In
1,4-dioxane; methanol; dichloromethane; toluene;
DOI:10.1021/ml400528y
- Guidance literature:
-
With
hydrogenchloride;
In
1,4-dioxane;
at 20 ℃;
for 48h;
Inert atmosphere;
DOI:10.1021/ml400528y
- Guidance literature:
-
Multi-step reaction with 2 steps
1: 3-[(diethoxyphosphinyl)oxy]-1,2,3-benzotriazin-4(3H)-one; N-ethyl-N,N-diisopropylamine / dichloromethane / 18 h / 20 °C / Inert atmosphere
2: hydrogenchloride / 1,4-dioxane / 48 h / 20 °C / Inert atmosphere
With
hydrogenchloride; N-ethyl-N,N-diisopropylamine; 3-[(diethoxyphosphinyl)oxy]-1,2,3-benzotriazin-4(3H)-one;
In
1,4-dioxane; dichloromethane;
DOI:10.1021/ml400528y