Technology Process of C23H21F2N5O4S
There total 4 articles about C23H21F2N5O4S which
guide to synthetic route it.
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synthetic route:
- Guidance literature:
-
With
3-chloro-benzenecarboperoxoic acid;
In
dichloromethane;
at 0 ℃;
for 2h;
DOI:10.1021/jm301549a
- Guidance literature:
-
Multi-step reaction with 5 steps
1.1: copper(l) iodide; sodium iodide; N,N-dimethylethylenediamine / 1,4-dioxane / 3 h / 140 °C / Inert atmosphere
2.1: zinc; nickel dibromide; [2,2]bipyridinyl / N,N-dimethyl-formamide / 2 h / 80 °C / Inert atmosphere
3.1: N-ethyl-N,N-diisopropylamine; HATU / 0.75 h / 20 °C
3.2: 3 h / 20 °C
3.3: 2 h
4.1: N-ethyl-N,N-diisopropylamine; 1-methyl-pyrrolidin-2-one / 0.25 h / 160 °C
5.1: 3-chloro-benzenecarboperoxoic acid / dichloromethane / 2 h / 0 °C
With
1-methyl-pyrrolidin-2-one; [2,2]bipyridinyl; copper(l) iodide; N,N-dimethylethylenediamine; N-ethyl-N,N-diisopropylamine; 3-chloro-benzenecarboperoxoic acid; HATU; sodium iodide; nickel dibromide; zinc;
In
1,4-dioxane; dichloromethane; N,N-dimethyl-formamide;
DOI:10.1021/jm301549a
- Guidance literature:
-
Multi-step reaction with 4 steps
1.1: zinc; nickel dibromide; [2,2]bipyridinyl / N,N-dimethyl-formamide / 2 h / 80 °C / Inert atmosphere
2.1: N-ethyl-N,N-diisopropylamine; HATU / 0.75 h / 20 °C
2.2: 3 h / 20 °C
2.3: 2 h
3.1: N-ethyl-N,N-diisopropylamine; 1-methyl-pyrrolidin-2-one / 0.25 h / 160 °C
4.1: 3-chloro-benzenecarboperoxoic acid / dichloromethane / 2 h / 0 °C
With
1-methyl-pyrrolidin-2-one; [2,2]bipyridinyl; N-ethyl-N,N-diisopropylamine; 3-chloro-benzenecarboperoxoic acid; HATU; nickel dibromide; zinc;
In
dichloromethane; N,N-dimethyl-formamide;
DOI:10.1021/jm301549a