Technology Process of 1-Methyl-4-((2S,3R)-3-phenyl-oxiranesulfonyl)-piperazine
There total 6 articles about 1-Methyl-4-((2S,3R)-3-phenyl-oxiranesulfonyl)-piperazine 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
potassium hydroxide; potassium hypochlorite; tetra(n-butyl)ammonium hydrogensulfate;
In
diethyl ether;
at 20 ℃;
for 14h;
DOI:10.1021/jm00395a010
- Guidance literature:
-
Multi-step reaction with 4 steps
1: CH2Cl2 / 3 h / Ambient temperature
2: 54 percent / t-BuOK / dioxane; 2-methyl-propan-2-ol / 3 h / Ambient temperature
3: 27 percent / aq. NaPO2H2 / 5percent Pd/BaSO4 / ethanol / 15 h / Heating
4: 48 percent / KOCl, conc. KOH, tetrabutylammonium hydrogen sulfate / diethyl ether / 14 h / 20 °C
With
potassium hydroxide; sodium hypophosphite; potassium hypochlorite; potassium tert-butylate; tetra(n-butyl)ammonium hydrogensulfate;
Pd-BaSO4;
In
1,4-dioxane; diethyl ether; ethanol; dichloromethane; tert-butyl alcohol;
DOI:10.1021/jm00395a010
- Guidance literature:
-
Multi-step reaction with 5 steps
1: 1.) Br2, 2.) NEt3 / 1.) CCl4, RT, 2.) Et2O, -5 deg C
2: CH2Cl2 / 3 h / Ambient temperature
3: 54 percent / t-BuOK / dioxane; 2-methyl-propan-2-ol / 3 h / Ambient temperature
4: 27 percent / aq. NaPO2H2 / 5percent Pd/BaSO4 / ethanol / 15 h / Heating
5: 48 percent / KOCl, conc. KOH, tetrabutylammonium hydrogen sulfate / diethyl ether / 14 h / 20 °C
With
potassium hydroxide; sodium hypophosphite; potassium hypochlorite; potassium tert-butylate; bromine; tetra(n-butyl)ammonium hydrogensulfate; triethylamine;
Pd-BaSO4;
In
1,4-dioxane; diethyl ether; ethanol; dichloromethane; tert-butyl alcohol;
DOI:10.1021/jm00395a010