Technology Process of ethyl 4-(4-(3-(5-((5-tert-butyloxazol-2-yl)methylthio)thiazol-2-yl)ureido)phenoxy)butanoate
There total 8 articles about ethyl 4-(4-(3-(5-((5-tert-butyloxazol-2-yl)methylthio)thiazol-2-yl)ureido)phenoxy)butanoate which
guide to synthetic route it.
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synthetic route:
- Guidance literature:
-
4-Nitrophenyl chloroformate; 2-amino-5-[[[5-(1,1-dimethylethyl)-2-oxazolyl]methyl]thio]-thiazole;
With
triethylamine;
In
dichloromethane;
at 0 ℃;
for 2h;
4-(4-aminofenossi)butirrato di etile;
In
dichloromethane;
at 20 ℃;
- Guidance literature:
-
Multi-step reaction with 6 steps
1.1: sodium azide / acetone / 25 °C
2.1: hydrogenchloride; hydrogen / palladium 10% on activated carbon / methanol
3.1: triethylamine / dichloromethane / 1.25 h / -10 - -5 °C
4.1: trichlorophosphate / 1 h / 105 °C
5.1: ethanol; sodium tetrahydroborate / acetone / 1 h / 20 °C
5.2: 1 h / Reflux
6.1: triethylamine / dichloromethane / 2 h / 0 °C
6.2: 20 °C
With
hydrogenchloride; sodium tetrahydroborate; sodium azide; ethanol; hydrogen; triethylamine; trichlorophosphate;
palladium 10% on activated carbon;
In
methanol; dichloromethane; acetone;
- Guidance literature:
-
Multi-step reaction with 5 steps
1.1: hydrogenchloride; hydrogen / palladium 10% on activated carbon / methanol
2.1: triethylamine / dichloromethane / 1.25 h / -10 - -5 °C
3.1: trichlorophosphate / 1 h / 105 °C
4.1: ethanol; sodium tetrahydroborate / acetone / 1 h / 20 °C
4.2: 1 h / Reflux
5.1: triethylamine / dichloromethane / 2 h / 0 °C
5.2: 20 °C
With
hydrogenchloride; sodium tetrahydroborate; ethanol; hydrogen; triethylamine; trichlorophosphate;
palladium 10% on activated carbon;
In
methanol; dichloromethane; acetone;