4-(tert-butyl)-N-(2-methyl-3-(1-methyl-5-((4-(morpholine-4-carbonyl)-3-nitrophenyl)amino)-6-oxo-1,6-dihydropyridin-3-yl)phenyl)benzamide

Base Information

Chemical Name:4-(tert-butyl)-N-(2-methyl-3-(1-methyl-5-((4-(morpholine-4-carbonyl)-3-nitrophenyl)amino)-6-oxo-1,6-dihydropyridin-3-yl)phenyl)benzamide
CAS No.:910234-22-9
Molecular Formula:C₃₄H₃₆N₆O₆
Molecular Weight:624.696
Hs Code.:

Synonyms:4-(tert-butyl)-N-(2-methyl-3-(1-methyl-5-((4-(morpholine-4-carbonyl)-3-nitrophenyl)amino)-6-oxo-1,6-dihydropyridin-3-yl)phenyl)benzamide

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Chemical Property of 4-(tert-butyl)-N-(2-methyl-3-(1-methyl-5-((4-(morpholine-4-carbonyl)-3-nitrophenyl)amino)-6-oxo-1,6-dihydropyridin-3-yl)phenyl)benzamide

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Technology Process of 4-(tert-butyl)-N-(2-methyl-3-(1-methyl-5-((4-(morpholine-4-carbonyl)-3-nitrophenyl)amino)-6-oxo-1,6-dihydropyridin-3-yl)phenyl)benzamide

There total 6 articles about 4-(tert-butyl)-N-(2-methyl-3-(1-methyl-5-((4-(morpholine-4-carbonyl)-3-nitrophenyl)amino)-6-oxo-1,6-dihydropyridin-3-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: 62.0%

: 910235-65-3
4-tert-butyl-N-[2-methyl-3-(4,4,5,5-tetramethyl-[1,2,3]dioxaborolan-2-yl)-phenyl]-benzamide

: 5-bromo-1-methyl-3-((4-(morpholine-4-carbonyl)-3-nitrophenyl)amino)pyridin-2(1H)-one

: 910234-22-9
4-(tert-butyl)-N-(2-methyl-3-(1-methyl-5-((4-(morpholine-4-carbonyl)-3-nitrophenyl)amino)-6-oxo-1,6-dihydropyridin-3-yl)phenyl)benzamide

Guidance literature:: With tetrakis(triphenylphosphine) palladium⁽⁰⁾; sodium carbonate; In 1,4-dioxane; water; at 110 ℃; Inert atmosphere;
DOI:10.1016/j.ejmech.2017.03.001

Reference yield:

: 98-73-7
4-(1,1-dimethylethyl)benzoic acid

: 910234-22-9
4-(tert-butyl)-N-(2-methyl-3-(1-methyl-5-((4-(morpholine-4-carbonyl)-3-nitrophenyl)amino)-6-oxo-1,6-dihydropyridin-3-yl)phenyl)benzamide

Guidance literature:: Multi-step reaction with 4 steps

1: oxalyl dichloride; N,N-dimethyl-formamide / dichloromethane / 4 h / 0 - 20 °C

2: N-ethyl-N,N-diisopropylamine / dichloromethane / 0.17 h / 0 - 20 °C

3: potassium acetate; (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride / 1,4-dioxane / 8 h / 100 °C / Inert atmosphere

4: sodium carbonate; tetrakis(triphenylphosphine) palladium⁽⁰⁾ / 1,4-dioxane; water / 110 °C / Inert atmosphere

With (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; tetrakis(triphenylphosphine) palladium⁽⁰⁾; oxalyl dichloride; potassium acetate; sodium carbonate; N-ethyl-N,N-diisopropylamine; N,N-dimethyl-formamide; In 1,4-dioxane; dichloromethane; water; 3: |Suzuki Coupling / 4: |Suzuki Coupling;
DOI:10.1016/j.ejmech.2017.03.001

Reference yield:

: 1710-98-1
p-tert-butyl benzoyl chloride

: 910234-22-9
4-(tert-butyl)-N-(2-methyl-3-(1-methyl-5-((4-(morpholine-4-carbonyl)-3-nitrophenyl)amino)-6-oxo-1,6-dihydropyridin-3-yl)phenyl)benzamide

Guidance literature:: Multi-step reaction with 3 steps

1: N-ethyl-N,N-diisopropylamine / dichloromethane / 0.17 h / 0 - 20 °C

2: potassium acetate; (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride / 1,4-dioxane / 8 h / 100 °C / Inert atmosphere

3: sodium carbonate; tetrakis(triphenylphosphine) palladium⁽⁰⁾ / 1,4-dioxane; water / 110 °C / Inert atmosphere

With (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; tetrakis(triphenylphosphine) palladium⁽⁰⁾; potassium acetate; sodium carbonate; N-ethyl-N,N-diisopropylamine; In 1,4-dioxane; dichloromethane; water; 2: |Suzuki Coupling / 3: |Suzuki Coupling;
DOI:10.1016/j.ejmech.2017.03.001