Technology Process of Boc-Hse(Bn)-Thr-OMe
There total 1 articles about Boc-Hse(Bn)-Thr-OMe which
guide to synthetic route it.
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synthetic route:
- Guidance literature:
-
L-threonine methyl ester hydrochloride;
With
N-ethyl-N,N-diisopropylamine;
In
N,N-dimethyl-formamide;
at 18 ℃;
for 0.5h;
(S)-2-((tert-butoxy)carbonylamino)-4-(phenylmethoxy)butyric acid;
With
diphenyl phosphoryl azide; N-ethyl-N,N-diisopropylamine;
In
N,N-dimethyl-formamide;
at 18 ℃;
for 16h;
DOI:10.1080/10610278.2012.688128
- Guidance literature:
-
With
(bis-(2-methoxyethyl)amino)sulfur trufluoride;
In
dichloromethane;
at -20 - 20 ℃;
for 7h;
Inert atmosphere;
DOI:10.1080/10610278.2012.688128
- Guidance literature:
-
Multi-step reaction with 8 steps
1.1: (bis-(2-methoxyethyl)amino)sulfur trufluoride / dichloromethane / 7 h / -20 - 20 °C / Inert atmosphere
2.1: Bromotrichloromethane; 1,8-diazabicyclo[5.4.0]undec-7-ene / dichloromethane / 6 h / -20 - 20 °C
3.1: water; sodium hydroxide / methanol / 2 h / 20 °C
3.2: pH 5
4.1: dicyclohexyl-carbodiimide / tetrahydrofuran / 16 h / 20 °C
5.1: dichloromethane / 2 h / 20 °C
6.1: N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide / 72 h / 20 °C
7.1: palladium 10% on activated carbon; hydrogen / methanol; ethyl acetate / 12 h / Inert atmosphere
8.1: trimethylamine hydrochloride; triethylamine / acetonitrile / 3 h / 0 °C
With
Bromotrichloromethane; palladium 10% on activated carbon; water; hydrogen; trimethylamine hydrochloride; 1,8-diazabicyclo[5.4.0]undec-7-ene; triethylamine; N-ethyl-N,N-diisopropylamine; dicyclohexyl-carbodiimide; sodium hydroxide; (bis-(2-methoxyethyl)amino)sulfur trufluoride;
In
tetrahydrofuran; methanol; dichloromethane; ethyl acetate; N,N-dimethyl-formamide; acetonitrile;
DOI:10.1080/10610278.2012.688128