Technology Process of C26H36N8O5
There total 6 articles about C26H36N8O5 which
guide to synthetic route it.
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synthetic route:
- Guidance literature:
-
C29H40N8O5;
With
trifluoroacetic acid;
at 20 ℃;
for 1h;
With
potassium carbonate;
In
methanol;
at 20 ℃;
for 1.5h;
- Guidance literature:
-
Multi-step reaction with 3 steps
1.1: sodium tris(acetoxy)borohydride / 1,2-dichloro-ethane / 20 °C
2.1: N-ethyl-N,N-diisopropylamine; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / dichloromethane / 20 °C
3.1: trifluoroacetic acid / 1 h / 20 °C
3.2: 1.5 h / 20 °C
With
sodium tris(acetoxy)borohydride; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine; trifluoroacetic acid;
In
dichloromethane; 1,2-dichloro-ethane;
- Guidance literature:
-
Multi-step reaction with 6 steps
1.1: toluene-4-sulfonic acid / water
1.2: 1 h
1.3: pH 8
2.1: triphenylphosphine; diethylazodicarboxylate / tetrahydrofuran / 20 °C
3.1: hydrazine hydrate / ethanol / 3 h / 20 °C / Reflux
4.1: sodium tris(acetoxy)borohydride / 1,2-dichloro-ethane / 20 °C
5.1: N-ethyl-N,N-diisopropylamine; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / dichloromethane / 20 °C
6.1: trifluoroacetic acid / 1 h / 20 °C
6.2: 1.5 h / 20 °C
With
sodium tris(acetoxy)borohydride; toluene-4-sulfonic acid; hydrazine hydrate; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine; triphenylphosphine; trifluoroacetic acid; diethylazodicarboxylate;
In
tetrahydrofuran; ethanol; dichloromethane; water; 1,2-dichloro-ethane;