Technology Process of Benzoic acid,
2-chloro-5-[[(7S)-7-[[(2R)-2-(3-chlorophenyl)-2-hydroxyethyl][(1,1-dimeth
ylethoxy)carbonyl]amino]-5,6,7,8-tetrahydro-2-naphthalenyl]oxy]-, methyl
ester
There total 9 articles about Benzoic acid,
2-chloro-5-[[(7S)-7-[[(2R)-2-(3-chlorophenyl)-2-hydroxyethyl][(1,1-dimeth
ylethoxy)carbonyl]amino]-5,6,7,8-tetrahydro-2-naphthalenyl]oxy]-, methyl
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:
-
With
copper diacetate; triethylamine;
In
dichloromethane;
at 20 ℃;
Molecular sieve;
Inert atmosphere;
DOI:10.1021/jm800222k
- Guidance literature:
-
Multi-step reaction with 5 steps
1: boron tribromide / dichloromethane / 4 - 20 °C / Inert atmosphere
2: palladium 10% on activated carbon; hydrogen / methanol / 2 h
3: ethanol / Reflux
4: tetrahydrofuran / 20 °C
5: copper diacetate; triethylamine / dichloromethane / 20 °C / Molecular sieve; Inert atmosphere
With
palladium 10% on activated carbon; hydrogen; copper diacetate; boron tribromide; triethylamine;
In
tetrahydrofuran; methanol; ethanol; dichloromethane;
DOI:10.1021/jm800222k
- Guidance literature:
-
Multi-step reaction with 4 steps
1: palladium 10% on activated carbon; hydrogen / methanol / 2 h
2: ethanol / Reflux
3: tetrahydrofuran / 20 °C
4: copper diacetate; triethylamine / dichloromethane / 20 °C / Molecular sieve; Inert atmosphere
With
palladium 10% on activated carbon; hydrogen; copper diacetate; triethylamine;
In
tetrahydrofuran; methanol; ethanol; dichloromethane;
DOI:10.1021/jm800222k