Technology Process of C28H37F2N6O8P
There total 16 articles about C28H37F2N6O8P which
guide to synthetic route it.
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synthetic route:
- Guidance literature:
-
With
hydrogenchloride;
In
1,4-dioxane; acetonitrile;
at 0 - 20 ℃;
for 1h;
- Guidance literature:
-
Multi-step reaction with 7 steps
1: 1,8-diazabicyclo[5.4.0]undec-7-ene / tetrahydrofuran / 3 h / Reflux
2: triethylamine tris(hydrogen fluoride); N-iodo-succinimide / acetonitrile / 2 h / 0 - 20 °C
3: silver nitrate / dichloromethane / 0 - 20 °C
4: 15-crown-5 / N,N-dimethyl-formamide / 72 h / 95 °C
5: ammonia / methanol / 18 h / 20 °C
6: 1-methyl-1H-imidazole / acetonitrile / 4 h / 0 - 5 °C
7: hydrogenchloride / 1,4-dioxane; acetonitrile / 1 h / 0 - 20 °C
With
1-methyl-1H-imidazole; hydrogenchloride; N-iodo-succinimide; 15-crown-5; ammonia; silver nitrate; 1,8-diazabicyclo[5.4.0]undec-7-ene; triethylamine tris(hydrogen fluoride);
In
tetrahydrofuran; 1,4-dioxane; methanol; dichloromethane; N,N-dimethyl-formamide; acetonitrile;
- Guidance literature:
-
Multi-step reaction with 8 steps
1: triphenylphosphine; pyridine; iodine / 20 °C
2: 1,8-diazabicyclo[5.4.0]undec-7-ene / tetrahydrofuran / 3 h / Reflux
3: triethylamine tris(hydrogen fluoride); N-iodo-succinimide / acetonitrile / 2 h / 0 - 20 °C
4: silver nitrate / dichloromethane / 0 - 20 °C
5: 15-crown-5 / N,N-dimethyl-formamide / 72 h / 95 °C
6: ammonia / methanol / 18 h / 20 °C
7: 1-methyl-1H-imidazole / acetonitrile / 4 h / 0 - 5 °C
8: hydrogenchloride / 1,4-dioxane; acetonitrile / 1 h / 0 - 20 °C
With
pyridine; 1-methyl-1H-imidazole; hydrogenchloride; N-iodo-succinimide; 15-crown-5; ammonia; iodine; silver nitrate; 1,8-diazabicyclo[5.4.0]undec-7-ene; triethylamine tris(hydrogen fluoride); triphenylphosphine;
In
tetrahydrofuran; 1,4-dioxane; methanol; dichloromethane; N,N-dimethyl-formamide; acetonitrile;