5-(6-(4-fluoro-1H-indol-2-yl)pyrazin-2-yl)-2-(4-fluorophenyl)-N-methyl-6-(N-methylmethylsulfonamido)benzofuran-3-carboxamide

Base Information

Chemical Name:5-(6-(4-fluoro-1H-indol-2-yl)pyrazin-2-yl)-2-(4-fluorophenyl)-N-methyl-6-(N-methylmethylsulfonamido)benzofuran-3-carboxamide
CAS No.:1426940-88-6
Molecular Formula:C₃₀H₂₃F₂N₅O₄S
Molecular Weight:587.607
Hs Code.:

Synonyms:5-(6-(4-fluoro-1H-indol-2-yl)pyrazin-2-yl)-2-(4-fluorophenyl)-N-methyl-6-(N-methylmethylsulfonamido)benzofuran-3-carboxamide

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Chemical Property of 5-(6-(4-fluoro-1H-indol-2-yl)pyrazin-2-yl)-2-(4-fluorophenyl)-N-methyl-6-(N-methylmethylsulfonamido)benzofuran-3-carboxamide

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Technology Process of 5-(6-(4-fluoro-1H-indol-2-yl)pyrazin-2-yl)-2-(4-fluorophenyl)-N-methyl-6-(N-methylmethylsulfonamido)benzofuran-3-carboxamide

There total 6 articles about 5-(6-(4-fluoro-1H-indol-2-yl)pyrazin-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: 56.7%

: 1333340-17-2
2-(4-fluorophenyl)-N-methyl-6-(N-methylmethylsulfonamido)-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzofuran-3-carboxamide

: 2-(6-chloropyrazin-2-yl)-4-fluoro-1H-indole

: 1426940-88-6
5-(6-(4-fluoro-1H-indol-2-yl)pyrazin-2-yl)-2-(4-fluorophenyl)-N-methyl-6-(N-methylmethylsulfonamido)benzofuran-3-carboxamide

Guidance literature:: With potassium phosphate; tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; XPhos; In 1,4-dioxane; water; at 110 ℃; Inert atmosphere;

Reference yield:

: 387-43-9
4-fluoroindole

: 1426940-88-6
5-(6-(4-fluoro-1H-indol-2-yl)pyrazin-2-yl)-2-(4-fluorophenyl)-N-methyl-6-(N-methylmethylsulfonamido)benzofuran-3-carboxamide

Guidance literature:: Multi-step reaction with 5 steps

1.1: dmap / tetrahydrofuran / 25 °C

2.1: n-butyllithium; diisopropylamine; Triisopropyl borate / tetrahydrofuran / 0.67 h / -78 °C

2.2: pH 6

3.1: (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; potassium phosphate / N,N-dimethyl-formamide / 80 °C / Inert atmosphere

4.1: hydrogenchloride / methanol / 2 h / 25 °C

5.1: potassium phosphate; tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; XPhos / 1,4-dioxane; water / 110 °C / Inert atmosphere

With hydrogenchloride; dmap; (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; potassium phosphate; tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; n-butyllithium; Triisopropyl borate; diisopropylamine; XPhos; In tetrahydrofuran; 1,4-dioxane; methanol; water; N,N-dimethyl-formamide; 3.1: |Suzuki Coupling / 5.1: |Suzuki Coupling;

Reference yield:

: tert-butyl 2-(6-chloropyrazin-2-yl)-4-fluoro-1H-indole-1-carboxylate

: 1426940-88-6
5-(6-(4-fluoro-1H-indol-2-yl)pyrazin-2-yl)-2-(4-fluorophenyl)-N-methyl-6-(N-methylmethylsulfonamido)benzofuran-3-carboxamide

Guidance literature:: Multi-step reaction with 2 steps

1: hydrogenchloride / methanol / 2 h / 25 °C

2: potassium phosphate; tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; XPhos / 1,4-dioxane; water / 110 °C / Inert atmosphere

With hydrogenchloride; potassium phosphate; tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; XPhos; In 1,4-dioxane; methanol; water; 2: |Suzuki Coupling;