Technology Process of C23H26ClN3O3S*ClH
There total 9 articles about C23H26ClN3O3S*ClH 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:
-
Multi-step reaction with 9 steps
1.1: n-butyllithium / tetrahydrofuran; hexane / 0.17 h / 0 °C / Inert atmosphere
1.2: 3 h / 20 °C / Inert atmosphere
2.1: hydroxylamine hydrochloride / ethanol / 6 h / Reflux
3.1: sodium tetrahydroborate / tetrahydrofuran; ethanol / 4 h / 0 °C
4.1: di-isopropyl azodicarboxylate; triphenylphosphine / tetrahydrofuran / 48 h / 20 °C
5.1: tin(II) chloride dihdyrate / N,N-dimethyl-formamide / 20 °C
6.1: benzotriazol-1-ol; dicyclohexyl-carbodiimide / tetrahydrofuran / 0.5 h
6.2: 48 h / 20 °C
7.1: hydrogenchloride / chloroform / 0.5 h / 0 °C
8.1: sodium cyanoborohydride / methanol / 24 h / 20 °C
9.1: hydrogenchloride / methanol / 0.5 h / 0 °C
With
hydrogenchloride; sodium tetrahydroborate; n-butyllithium; tin(II) chloride dihdyrate; di-isopropyl azodicarboxylate; hydroxylamine hydrochloride; sodium cyanoborohydride; benzotriazol-1-ol; dicyclohexyl-carbodiimide; triphenylphosphine;
In
tetrahydrofuran; methanol; ethanol; hexane; chloroform; N,N-dimethyl-formamide;
4.1: Mitsunobu reaction;
DOI:10.1016/j.ejps.2010.11.010
- Guidance literature:
-
Multi-step reaction with 3 steps
1: hydrogenchloride / chloroform / 0.5 h / 0 °C
2: sodium cyanoborohydride / methanol / 24 h / 20 °C
3: hydrogenchloride / methanol / 0.5 h / 0 °C
With
hydrogenchloride; sodium cyanoborohydride;
In
methanol; chloroform;
DOI:10.1016/j.ejps.2010.11.010