Technology Process of C27H34N4O2S2
There total 5 articles about C27H34N4O2S2 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:
-
With
acetic acid;
In
methanol; 1,2-dichloro-ethane;
at 20 - 55 ℃;
optical yield given as %de;
DOI:10.1016/j.bmcl.2011.11.126
- Guidance literature:
-
Multi-step reaction with 4 steps
1: hydroquinone / toluene / 24 h / 170 °C
2: water; lithium hydroxide / tetrahydrofuran / 2 h / 60 °C
3: benzotriazol-1-ol; N-ethyl-N,N-diisopropylamine / tetrahydrofuran / 20 °C
4: acetic acid / methanol; 1,2-dichloro-ethane / 20 - 55 °C
With
water; benzotriazol-1-ol; acetic acid; N-ethyl-N,N-diisopropylamine; hydroquinone; lithium hydroxide;
In
tetrahydrofuran; methanol; 1,2-dichloro-ethane; toluene;
1: Diels-Alder reaction;
DOI:10.1016/j.bmcl.2011.11.126
- Guidance literature:
-
Multi-step reaction with 3 steps
1: water; lithium hydroxide / tetrahydrofuran / 2 h / 60 °C
2: benzotriazol-1-ol; N-ethyl-N,N-diisopropylamine / tetrahydrofuran / 20 °C
3: acetic acid / methanol; 1,2-dichloro-ethane / 20 - 55 °C
With
water; benzotriazol-1-ol; acetic acid; N-ethyl-N,N-diisopropylamine; lithium hydroxide;
In
tetrahydrofuran; methanol; 1,2-dichloro-ethane;
DOI:10.1016/j.bmcl.2011.11.126