4-(tert-butyl)-N-(2-methyl-3-(6-methyl-7-oxo-6,7-dihydro-1H-pyrrolo[2,3-c]pyridin-4-yl)phenyl)benzamide

Base Information

Chemical Name:4-(tert-butyl)-N-(2-methyl-3-(6-methyl-7-oxo-6,7-dihydro-1H-pyrrolo[2,3-c]pyridin-4-yl)phenyl)benzamide
CAS No.:1622302-83-3
Molecular Formula:C₂₆H₂₇N₃O₂
Molecular Weight:413.519
Hs Code.:

Synonyms:4-(tert-butyl)-N-(2-methyl-3-(6-methyl-7-oxo-6,7-dihydro-1H-pyrrolo[2,3-c]pyridin-4-yl)phenyl)benzamide

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Chemical Property of 4-(tert-butyl)-N-(2-methyl-3-(6-methyl-7-oxo-6,7-dihydro-1H-pyrrolo[2,3-c]pyridin-4-yl)phenyl)benzamide

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Technology Process of 4-(tert-butyl)-N-(2-methyl-3-(6-methyl-7-oxo-6,7-dihydro-1H-pyrrolo[2,3-c]pyridin-4-yl)phenyl)benzamide

There total 14 articles about 4-(tert-butyl)-N-(2-methyl-3-(6-methyl-7-oxo-6,7-dihydro-1H-pyrrolo[2,3-c]pyridin-4-yl)phenyl)benzamide 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: 23.0%

: 1622303-43-8
4-(tert-butyl)-N-(2-methyl-3-(6-methyl-7-oxo-1-tosyl-6,7-dihydro-1H-pyrrolo[2,3-c]pyridin-4-yl)phenyl)benzamide

: 1622302-83-3
4-(tert-butyl)-N-(2-methyl-3-(6-methyl-7-oxo-6,7-dihydro-1H-pyrrolo[2,3-c]pyridin-4-yl)phenyl)benzamide

Guidance literature:: With water; sodium hydroxide; In ethanol; at 20 ℃; for 3h;

Reference yield:

: 67443-38-3
5-bromo-2-chloro-3-nitropyridine

: 1622302-83-3
4-(tert-butyl)-N-(2-methyl-3-(6-methyl-7-oxo-6,7-dihydro-1H-pyrrolo[2,3-c]pyridin-4-yl)phenyl)benzamide

Guidance literature:: Multi-step reaction with 6 steps

1.1: tetrahydrofuran / 8 h / -78 - -20 °C

2.1: sodium hydride / tetrahydrofuran / 0.25 h / 0 - 5 °C / Inert atmosphere

2.2: 6 h / 0 - 20 °C

3.1: acetic acid / 48 h / Reflux

4.1: caesium carbonate / N,N-dimethyl-formamide / 3 h / 20 °C

5.1: dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH₂Cl₂; potassium carbonate / 1,4-dioxane / 6 h / 100 °C / Sealed tube; Inert atmosphere

6.1: water; sodium hydroxide / ethanol / 3 h / 20 °C

With dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH₂Cl₂; water; sodium hydride; potassium carbonate; caesium carbonate; acetic acid; sodium hydroxide; In tetrahydrofuran; 1,4-dioxane; ethanol; N,N-dimethyl-formamide;

Reference yield:

: 1258960-27-8
4-bromo-7-chloro-1-p-toluenesulfonyl-1H-pyrrolo[2,3-c]pyridine

: 1622302-83-3
4-(tert-butyl)-N-(2-methyl-3-(6-methyl-7-oxo-6,7-dihydro-1H-pyrrolo[2,3-c]pyridin-4-yl)phenyl)benzamide

Guidance literature:: Multi-step reaction with 4 steps

1: acetic acid / 48 h / Reflux

2: caesium carbonate / N,N-dimethyl-formamide / 3 h / 20 °C

3: dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH₂Cl₂; potassium carbonate / 1,4-dioxane / 6 h / 100 °C / Sealed tube; Inert atmosphere

4: water; sodium hydroxide / ethanol / 3 h / 20 °C

With dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH₂Cl₂; water; potassium carbonate; caesium carbonate; acetic acid; sodium hydroxide; In 1,4-dioxane; ethanol; N,N-dimethyl-formamide;