Technology Process of C18H25N3O4S
There total 7 articles about C18H25N3O4S 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:
-
C12H15N3O2S; dimethyl sulfate;
In
acetonitrile;
at 50 ℃;
for 2h;
di-tert-butyl dicarbonate;
With
triethylamine;
In
acetonitrile;
at 20 ℃;
for 2.5h;
- Guidance literature:
-
Multi-step reaction with 7 steps
1.1: sodium hydride / diethyl ether; dimethyl sulfoxide; mineral oil / 3.58 h / 20 - 35 °C
2.1: water; sulfuric acid / 8 h / Reflux
3.1: triethylamine; diphenyl phosphoryl azide / toluene / 1.17 h / 20 - 100 °C
3.2: 3 h / 100 °C
4.1: water; lithium hydroxide / dimethyl sulfoxide / 2 h / 110 °C
5.1: acetone / 1 h / 20 °C
6.1: sodium hydroxide; water / methanol / 0.17 h / 50 °C
7.1: acetonitrile / 2 h / 50 °C
7.2: 2.5 h / 20 °C
With
sulfuric acid; diphenyl phosphoryl azide; water; sodium hydride; triethylamine; sodium hydroxide; lithium hydroxide;
In
methanol; diethyl ether; dimethyl sulfoxide; acetone; toluene; acetonitrile; mineral oil;
- Guidance literature:
-
Multi-step reaction with 5 steps
1.1: triethylamine; diphenyl phosphoryl azide / toluene / 1.17 h / 20 - 100 °C
1.2: 3 h / 100 °C
2.1: water; lithium hydroxide / dimethyl sulfoxide / 2 h / 110 °C
3.1: acetone / 1 h / 20 °C
4.1: sodium hydroxide; water / methanol / 0.17 h / 50 °C
5.1: acetonitrile / 2 h / 50 °C
5.2: 2.5 h / 20 °C
With
diphenyl phosphoryl azide; water; triethylamine; sodium hydroxide; lithium hydroxide;
In
methanol; dimethyl sulfoxide; acetone; toluene; acetonitrile;