Technology Process of methanesulfonic acid 3-[2-methyl-4-(4-methylsulfanyl-phenyl)-1,2,3,4-tetrahydro-isoquinolin-7-yloxy]-propyl ester
There total 8 articles about methanesulfonic acid 3-[2-methyl-4-(4-methylsulfanyl-phenyl)-1,2,3,4-tetrahydro-isoquinolin-7-yloxy]-propyl ester 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 5 steps
1: 100 percent / NaBH4 / methanol; H2O / 18.5 h / 0 - 23 °C
2: (i-Pr)2NEt / tetrahydrofuran / 0.75 h / 23 °C
3: methanesulfonic acid / 18 h / 60 °C
4: NaCNBH3 / methanol / 0.08 h / 23 °C
5: Et3N / CH2Cl2 / 0.33 h / 0 - 23 °C
With
sodium tetrahydroborate; methanesulfonic acid; sodium cyanoborohydride; triethylamine; N-ethyl-N,N-diisopropylamine;
In
tetrahydrofuran; methanol; dichloromethane; water;
DOI:10.1016/j.bmcl.2006.11.036
- Guidance literature:
-
Multi-step reaction with 4 steps
1: (i-Pr)2NEt / tetrahydrofuran / 0.75 h / 23 °C
2: methanesulfonic acid / 18 h / 60 °C
3: NaCNBH3 / methanol / 0.08 h / 23 °C
4: Et3N / CH2Cl2 / 0.33 h / 0 - 23 °C
With
methanesulfonic acid; sodium cyanoborohydride; triethylamine; N-ethyl-N,N-diisopropylamine;
In
tetrahydrofuran; methanol; dichloromethane;
DOI:10.1016/j.bmcl.2006.11.036