Technology Process of (2S,2'S,6'R,8'R)-N-{6'-[4''-(tert-butyldiphenylsilyloxy)-1''-butyl]-8'-phenyl-1'-aza-9'-oxabicyclo[4.3.0]nonan-2'-ylcarbonyl}bornane-10,2-sultam
There total 13 articles about (2S,2'S,6'R,8'R)-N-{6'-[4''-(tert-butyldiphenylsilyloxy)-1''-butyl]-8'-phenyl-1'-aza-9'-oxabicyclo[4.3.0]nonan-2'-ylcarbonyl}bornane-10,2-sultam 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 6 steps
1.1: 98 percent / CrO3; H2SO4 / acetone / 3 h / 0 °C
2.1: Et3N / tetrahydrofuran / 1 h / 25 °C
3.1: n-BuLi; pyren-1-ylacetic acid / tetrahydrofuran; hexane / 0.33 h / -78 °C
3.2: 3.54 g / tetrahydrofuran; hexane / 1.5 h / 25 °C
4.1: NaHMDS / tetrahydrofuran / 0.02 h / -78 °C
4.2: 1-chloro-1-nitrosocyclohexane / tetrahydrofuran / 0.5 h / -78 °C
4.3: 77 percent / aq. HCl / tetrahydrofuran / 1 h / 25 °C
5.1: toluene / 7 h / 75 °C
6.1: 2.7 g / quinol / 6 h / 80 °C
With
chromium(VI) oxide; n-butyllithium; sulfuric acid; 1-pyreneacetic acid; sodium hexamethyldisilazane; triethylamine; hydroquinone;
In
tetrahydrofuran; hexane; acetone; toluene;
DOI:10.1039/b200328g
- Guidance literature:
-
Multi-step reaction with 5 steps
1.1: Et3N / tetrahydrofuran / 1 h / 25 °C
2.1: n-BuLi; pyren-1-ylacetic acid / tetrahydrofuran; hexane / 0.33 h / -78 °C
2.2: 3.54 g / tetrahydrofuran; hexane / 1.5 h / 25 °C
3.1: NaHMDS / tetrahydrofuran / 0.02 h / -78 °C
3.2: 1-chloro-1-nitrosocyclohexane / tetrahydrofuran / 0.5 h / -78 °C
3.3: 77 percent / aq. HCl / tetrahydrofuran / 1 h / 25 °C
4.1: toluene / 7 h / 75 °C
5.1: 2.7 g / quinol / 6 h / 80 °C
With
n-butyllithium; 1-pyreneacetic acid; sodium hexamethyldisilazane; triethylamine; hydroquinone;
In
tetrahydrofuran; hexane; toluene;
DOI:10.1039/b200328g
- Guidance literature:
-
Multi-step reaction with 7 steps
1.1: 100 percent / BCl3*SMe2 / CH2Cl2
2.1: 98 percent / CrO3; H2SO4 / acetone / 3 h / 0 °C
3.1: Et3N / tetrahydrofuran / 1 h / 25 °C
4.1: n-BuLi; pyren-1-ylacetic acid / tetrahydrofuran; hexane / 0.33 h / -78 °C
4.2: 3.54 g / tetrahydrofuran; hexane / 1.5 h / 25 °C
5.1: NaHMDS / tetrahydrofuran / 0.02 h / -78 °C
5.2: 1-chloro-1-nitrosocyclohexane / tetrahydrofuran / 0.5 h / -78 °C
5.3: 77 percent / aq. HCl / tetrahydrofuran / 1 h / 25 °C
6.1: toluene / 7 h / 75 °C
7.1: 2.7 g / quinol / 6 h / 80 °C
With
chromium(VI) oxide; n-butyllithium; boron trichloride - methyl sulfide complex; sulfuric acid; 1-pyreneacetic acid; sodium hexamethyldisilazane; triethylamine; hydroquinone;
In
tetrahydrofuran; hexane; dichloromethane; acetone; toluene;
DOI:10.1039/b200328g