Technology Process of 3-(6-(1-methyl-1H-pyrazol-4-yl)-5-nitro-1-((2-(trimethylsilyl)-ethoxy)methyl)-1H-indazol-3-yl)benzenesulfonamide
There total 7 articles about 3-(6-(1-methyl-1H-pyrazol-4-yl)-5-nitro-1-((2-(trimethylsilyl)-ethoxy)methyl)-1H-indazol-3-yl)benzenesulfonamide which
guide to synthetic route it.
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synthetic route:
- Guidance literature:
-
3-iodo-6-(1-methyl-1H-pyrazol-4-yl)-5-nitro-1H-indazole; (2-trimethylethylsilylethoxy)methyl chloride;
With
sodium hydride;
In
N,N-dimethyl-formamide;
at 0 - 20 ℃;
for 0.666667h;
3-(dihydroxyboranyl)benzene-1-sulfonamide;
With
dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH2Cl2; sodium carbonate;
In
tetrahydrofuran; water;
for 3h;
Inert atmosphere;
Reflux;
DOI:10.1021/jm4000215
- Guidance literature:
-
Multi-step reaction with 3 steps
1.1: tetrabutyl ammonium fluoride; ethylenediamine / tetrahydrofuran / 8 h / Reflux
2.1: iodine; potassium hydroxide / N,N-dimethyl-formamide / 2 h / 20 °C
3.1: sodium hydride / N,N-dimethyl-formamide / 0.67 h / 0 - 20 °C
3.2: 3 h / Inert atmosphere; Reflux
With
tetrabutyl ammonium fluoride; iodine; sodium hydride; ethylenediamine; potassium hydroxide;
In
tetrahydrofuran; N,N-dimethyl-formamide;
1.1: |Suzuki Coupling / 3.2: |Suzuki Coupling;
DOI:10.1021/jm4000215
- Guidance literature:
-
Multi-step reaction with 4 steps
1.1: dichloro[1,1'-bis(di-t-butylphosphino)ferrocene]palladium(II); potassium carbonate / tetrahydrofuran; water / 3.5 h / Reflux; Inert atmosphere
2.1: tetrabutyl ammonium fluoride; ethylenediamine / tetrahydrofuran / 8 h / Reflux
3.1: iodine; potassium hydroxide / N,N-dimethyl-formamide / 2 h / 20 °C
4.1: sodium hydride / N,N-dimethyl-formamide / 0.67 h / 0 - 20 °C
4.2: 3 h / Inert atmosphere; Reflux
With
dichloro[1,1'-bis(di-t-butylphosphino)ferrocene]palladium(II); tetrabutyl ammonium fluoride; iodine; sodium hydride; potassium carbonate; ethylenediamine; potassium hydroxide;
In
tetrahydrofuran; water; N,N-dimethyl-formamide;
1.1: |Suzuki Coupling / 2.1: |Suzuki Coupling / 4.2: |Suzuki Coupling;
DOI:10.1021/jm4000215