5-(11-fluoroindolo[1,2-h][1,7]naphthyridin-2-yl)-2-(4-fluorophenyl)-N-methyl-6-(N-methylmethylsulfonamido)benzofuran-3-carboxamide

Base Information

Chemical Name:5-(11-fluoroindolo[1,2-h][1,7]naphthyridin-2-yl)-2-(4-fluorophenyl)-N-methyl-6-(N-methylmethylsulfonamido)benzofuran-3-carboxamide
CAS No.:1621704-90-2
Molecular Formula:C₃₃H₂₄F₂N₄O₄S
Molecular Weight:610.641
Hs Code.:

Synonyms:5-(11-fluoroindolo[1,2-h][1,7]naphthyridin-2-yl)-2-(4-fluorophenyl)-N-methyl-6-(N-methylmethylsulfonamido)benzofuran-3-carboxamide

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Chemical Property of 5-(11-fluoroindolo[1,2-h][1,7]naphthyridin-2-yl)-2-(4-fluorophenyl)-N-methyl-6-(N-methylmethylsulfonamido)benzofuran-3-carboxamide

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Technology Process of 5-(11-fluoroindolo[1,2-h][1,7]naphthyridin-2-yl)-2-(4-fluorophenyl)-N-methyl-6-(N-methylmethylsulfonamido)benzofuran-3-carboxamide

There total 9 articles about 5-(11-fluoroindolo[1,2-h][1,7]naphthyridin-2-yl)-2-(4-fluorophenyl)-N-methyl-6-(N-methylmethylsulfonamido)benzofuran-3-carboxamide 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: 44.0%

: C₃₄H₂₈F₂N₄O₅S

: 1621704-90-2
5-(11-fluoroindolo[1,2-h][1,7]naphthyridin-2-yl)-2-(4-fluorophenyl)-N-methyl-6-(N-methylmethylsulfonamido)benzofuran-3-carboxamide

Guidance literature:: With hydrogenchloride; In 1,4-dioxane; at 70 ℃; for 2h;
DOI:10.1016/j.bmcl.2018.10.045

Reference yield:

: 148493-37-2
2,6-dichloro-3-iodo-pyridine

: 1621704-90-2
5-(11-fluoroindolo[1,2-h][1,7]naphthyridin-2-yl)-2-(4-fluorophenyl)-N-methyl-6-(N-methylmethylsulfonamido)benzofuran-3-carboxamide

Guidance literature:: Multi-step reaction with 4 steps

1: caesium carbonate; dichloro[1,1'-bis(di-t-butylphosphino)ferrocene]palladium(II) / water; 1,4-dioxane / 70 °C / Inert atmosphere

2: caesium carbonate; dichloro[1,1'-bis(di-t-butylphosphino)ferrocene]palladium(II) / water; 1,4-dioxane / 90 °C / Inert atmosphere

3: caesium carbonate; dichloro[1,1'-bis(di-t-butylphosphino)ferrocene]palladium(II) / water; 1,4-dioxane / 3 h / 90 °C / Inert atmosphere

4: sodium iodide; chloro-trimethyl-silane / acetonitrile / 3 h / 20 °C

With chloro-trimethyl-silane; dichloro[1,1'-bis(di-t-butylphosphino)ferrocene]palladium(II); caesium carbonate; sodium iodide; In 1,4-dioxane; water; acetonitrile;

Reference yield:

: 1621706-09-9
(E)-6-bromo-2-chloro-3-(2-ethoxyvinyl)pyridine

: 1621704-90-2
5-(11-fluoroindolo[1,2-h][1,7]naphthyridin-2-yl)-2-(4-fluorophenyl)-N-methyl-6-(N-methylmethylsulfonamido)benzofuran-3-carboxamide

Guidance literature:: Multi-step reaction with 3 steps

1: (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; caesium carbonate / water; 1,4-dioxane / 16.12 h / 60 °C / Inert atmosphere

2: caesium carbonate; dichloro[1,1'-bis(di-t-butylphosphino)ferrocene]palladium(II) / water; 1,4-dioxane / 3 h / 90 °C / Inert atmosphere

3: sodium iodide; chloro-trimethyl-silane / acetonitrile / 3 h / 20 °C

With (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; chloro-trimethyl-silane; dichloro[1,1'-bis(di-t-butylphosphino)ferrocene]palladium(II); caesium carbonate; sodium iodide; In 1,4-dioxane; water; acetonitrile;