2-bromo-3-cyclohexyl-6-(N,N-dimethylsulfamoylcarbamoyl)-1-((2-(trimethylsilyl)ethoxy)methyl)-1H-pyrrolo[2,3-b]pyridine 7-oxide

Base Information

Chemical Name:2-bromo-3-cyclohexyl-6-(N,N-dimethylsulfamoylcarbamoyl)-1-((2-(trimethylsilyl)ethoxy)methyl)-1H-pyrrolo[2,3-b]pyridine 7-oxide
CAS No.:1049796-90-8
Molecular Formula:C₂₂H₃₅BrN₄O₅SSi
Molecular Weight:575.599
Hs Code.:

Synonyms:2-bromo-3-cyclohexyl-6-(N,N-dimethylsulfamoylcarbamoyl)-1-((2-(trimethylsilyl)ethoxy)methyl)-1H-pyrrolo[2,3-b]pyridine 7-oxide

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Chemical Property of 2-bromo-3-cyclohexyl-6-(N,N-dimethylsulfamoylcarbamoyl)-1-((2-(trimethylsilyl)ethoxy)methyl)-1H-pyrrolo[2,3-b]pyridine 7-oxide

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Technology Process of 2-bromo-3-cyclohexyl-6-(N,N-dimethylsulfamoylcarbamoyl)-1-((2-(trimethylsilyl)ethoxy)methyl)-1H-pyrrolo[2,3-b]pyridine 7-oxide

There total 6 articles about 2-bromo-3-cyclohexyl-6-(N,N-dimethylsulfamoylcarbamoyl)-1-((2-(trimethylsilyl)ethoxy)methyl)-1H-pyrrolo[2,3-b]pyridine 7-oxide 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:

Reference yield: 33.0%

: 3984-14-3
N,N-dimethylsulfamide

: 1049796-88-4
2-bromo-3-cyclohexyl-1-((2-(trimethylsilyl)ethoxy)methyl)-1H-pyrrolo[2,3-b]pyridine 7-oxide

: 530-62-1
1,1'-carbonyldiimidazole

: 1049796-90-8
2-bromo-3-cyclohexyl-6-(N,N-dimethylsulfamoylcarbamoyl)-1-((2-(trimethylsilyl)ethoxy)methyl)-1H-pyrrolo[2,3-b]pyridine 7-oxide

Guidance literature:: 2-bromo-3-cyclohexyl-1-((2-(trimethylsilyl)ethoxy)methyl)-1H-pyrrolo[2,3-b]pyridine 7-oxide; With lithium diisopropyl amide; In tetrahydrofuran; at -78 ℃; for 0.5h;

1,1'-carbonyldiimidazole; In tetrahydrofuran; at 50 ℃; for 2h;

N,N-dimethylsulfamide; With 1,8-diazabicyclo[5.4.0]undec-7-ene; In tetrahydrofuran; at 20 ℃; for 2.5h;

Reference yield:

: 494799-64-3
3-cyclohexenyl-1H-pyrrolo[2,3-b]pyridine

: 1049796-90-8
2-bromo-3-cyclohexyl-6-(N,N-dimethylsulfamoylcarbamoyl)-1-((2-(trimethylsilyl)ethoxy)methyl)-1H-pyrrolo[2,3-b]pyridine 7-oxide

Guidance literature:: Multi-step reaction with 4 steps

1.1: hydrogen / 20% Pd(OH)2 on carbon / tetrahydrofuran; ethanol / 144 h

2.1: pyridinium hydrobromide perbromide / tetrahydrofuran / 4 h / Heating / reflux

3.1: 3-chloro-benzenecarboperoxoic acid / 1,2-dimethoxyethane / 1 h / 20 °C

3.2: 1.17 h / 20 °C

4.1: lithium diisopropyl amide / tetrahydrofuran / 0.5 h / -78 °C

4.2: 2 h / 50 °C

4.3: 2.5 h / 20 °C

With pyridinium hydrobromide perbromide; hydrogen; 3-chloro-benzenecarboperoxoic acid; lithium diisopropyl amide; 20% Pd(OH)2 on carbon; In tetrahydrofuran; 1,2-dimethoxyethane; ethanol;

Reference yield:

: 271-63-6
7-Azaindole

: 1049796-90-8
2-bromo-3-cyclohexyl-6-(N,N-dimethylsulfamoylcarbamoyl)-1-((2-(trimethylsilyl)ethoxy)methyl)-1H-pyrrolo[2,3-b]pyridine 7-oxide

Guidance literature:: Multi-step reaction with 5 steps

1.1: sodium hydride / methanol / 24 h / 0 °C / Heating / reflux

2.1: hydrogen / 20% Pd(OH)2 on carbon / tetrahydrofuran; ethanol / 144 h

3.1: pyridinium hydrobromide perbromide / tetrahydrofuran / 4 h / Heating / reflux

4.1: 3-chloro-benzenecarboperoxoic acid / 1,2-dimethoxyethane / 1 h / 20 °C

4.2: 1.17 h / 20 °C

5.1: lithium diisopropyl amide / tetrahydrofuran / 0.5 h / -78 °C

5.2: 2 h / 50 °C

5.3: 2.5 h / 20 °C

With pyridinium hydrobromide perbromide; hydrogen; sodium hydride; 3-chloro-benzenecarboperoxoic acid; lithium diisopropyl amide; 20% Pd(OH)2 on carbon; In tetrahydrofuran; methanol; 1,2-dimethoxyethane; ethanol;