N-[5-[3-bromo-2-({[4-(methyloxy)phenyl]methyl}amino)-6-quinolinyl]-2-(methyloxy)-3-pyridinyl]benzenesulfonamide

Base Information

Chemical Name:N-[5-[3-bromo-2-({[4-(methyloxy)phenyl]methyl}amino)-6-quinolinyl]-2-(methyloxy)-3-pyridinyl]benzenesulfonamide
CAS No.:1366131-65-8
Molecular Formula:C₂₉H₂₅BrN₄O₄S
Molecular Weight:605.512
Hs Code.:

Synonyms:N-[5-[3-bromo-2-({[4-(methyloxy)phenyl]methyl}amino)-6-quinolinyl]-2-(methyloxy)-3-pyridinyl]benzenesulfonamide

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Chemical Property of N-[5-[3-bromo-2-({[4-(methyloxy)phenyl]methyl}amino)-6-quinolinyl]-2-(methyloxy)-3-pyridinyl]benzenesulfonamide

Chemical Property:

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Technology Process of N-[5-[3-bromo-2-({[4-(methyloxy)phenyl]methyl}amino)-6-quinolinyl]-2-(methyloxy)-3-pyridinyl]benzenesulfonamide

There total 9 articles about N-[5-[3-bromo-2-({[4-(methyloxy)phenyl]methyl}amino)-6-quinolinyl]-2-(methyloxy)-3-pyridinyl]benzenesulfonamide 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: 64.0%

3-bromo-6-iodo-N-{[4-(methyloxy)phenyl]methyl}-2-quinolinamine: 1366128-90-6
3-bromo-6-iodo-N-{[4-(methyloxy)phenyl]methyl}-2-quinolinamine

: 1083326-67-3
N-(2-methoxy-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin-3-yl)benzenesulfonamide

: 1366131-65-8
N-[5-[3-bromo-2-({[4-(methyloxy)phenyl]methyl}amino)-6-quinolinyl]-2-(methyloxy)-3-pyridinyl]benzenesulfonamide

Guidance literature:: With caesium carbonate; dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH₂Cl₂; In tetrahydrofuran; water; at 100 ℃; for 18h; Inert atmosphere; Sealed tube;

Reference yield:

: 98-09-9
benzenesulfonyl chloride

: 1366131-65-8
N-[5-[3-bromo-2-({[4-(methyloxy)phenyl]methyl}amino)-6-quinolinyl]-2-(methyloxy)-3-pyridinyl]benzenesulfonamide

Guidance literature:: Multi-step reaction with 3 steps

1: pyridine / 18 h / 20 °C

2: potassium acetate / dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH₂Cl₂ / 1,4-dioxane / 1.5 h / 80 °C

3: caesium carbonate / dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH₂Cl₂ / tetrahydrofuran; water / 18 h / 100 °C / Inert atmosphere; Sealed tube

With pyridine; potassium acetate; caesium carbonate; dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH₂Cl₂; In tetrahydrofuran; 1,4-dioxane; water; 2: Suzuki Coupling / 3: Suzuki Coupling;

Reference yield:

: 540-37-4
p-aminoiodobenzene

: 1366131-65-8
N-[5-[3-bromo-2-({[4-(methyloxy)phenyl]methyl}amino)-6-quinolinyl]-2-(methyloxy)-3-pyridinyl]benzenesulfonamide

Guidance literature:: Multi-step reaction with 6 steps

1: pyridine / dichloromethane / 2 h / 20 °C

2: sulfuric acid / 2 h / 0 - 20 °C

3: N-Bromosuccinimide / dichloromethane; N,N-dimethyl-formamide / 22 h / 20 °C

4: trichlorophosphate / 1 h / 100 °C

5: triethylamine / butan-1-ol / 29 h / 135 °C / Sealed tube

6: caesium carbonate / dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH₂Cl₂ / tetrahydrofuran; water / 18 h / 100 °C / Inert atmosphere; Sealed tube

With pyridine; N-Bromosuccinimide; sulfuric acid; caesium carbonate; triethylamine; trichlorophosphate; dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH₂Cl₂; In tetrahydrofuran; dichloromethane; water; N,N-dimethyl-formamide; butan-1-ol; 6: Suzuki Coupling;