N-(2-(piperidin-1-yl)ethyl)-2-(3-((4-(3-(pyridin-3-ylmethoxy)phenyl)-7-tosyl-7H-pyrrolo[2,3-d]pyrimidin-2-yl)amino)phenyl)acetamide

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Chemical Name:N-(2-(piperidin-1-yl)ethyl)-2-(3-((4-(3-(pyridin-3-ylmethoxy)phenyl)-7-tosyl-7H-pyrrolo[2,3-d]pyrimidin-2-yl)amino)phenyl)acetamide
CAS No.:1616474-18-0
Molecular Formula:C₄₀H₄₁N₇O₄S
Molecular Weight:715.876
Hs Code.:

Synonyms:N-(2-(piperidin-1-yl)ethyl)-2-(3-((4-(3-(pyridin-3-ylmethoxy)phenyl)-7-tosyl-7H-pyrrolo[2,3-d]pyrimidin-2-yl)amino)phenyl)acetamide

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Chemical Property of N-(2-(piperidin-1-yl)ethyl)-2-(3-((4-(3-(pyridin-3-ylmethoxy)phenyl)-7-tosyl-7H-pyrrolo[2,3-d]pyrimidin-2-yl)amino)phenyl)acetamide

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Technology Process of N-(2-(piperidin-1-yl)ethyl)-2-(3-((4-(3-(pyridin-3-ylmethoxy)phenyl)-7-tosyl-7H-pyrrolo[2,3-d]pyrimidin-2-yl)amino)phenyl)acetamide

There total 11 articles about N-(2-(piperidin-1-yl)ethyl)-2-(3-((4-(3-(pyridin-3-ylmethoxy)phenyl)-7-tosyl-7H-pyrrolo[2,3-d]pyrimidin-2-yl)amino)phenyl)acetamide 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: 72.0%

: 1498710-52-3
2-(3-aminophenyl)-N-(2-(piperidin-1-yl)ethyl)acetamide

: 1616474-11-3
2-chloro-4-(3-(pyridin-3-ylmethoxy)phenyl)-7-tosyl-7H-pyrrolo[2,3-d]pyrimidine

: 1616474-18-0
N-(2-(piperidin-1-yl)ethyl)-2-(3-((4-(3-(pyridin-3-ylmethoxy)phenyl)-7-tosyl-7H-pyrrolo[2,3-d]pyrimidin-2-yl)amino)phenyl)acetamide

Guidance literature:: With tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; potassium carbonate; XPhos; In tert-butyl alcohol; for 16h; Inert atmosphere; Reflux;
DOI:10.1016/j.tet.2014.05.033

Reference yield:

: 6959-48-4
3-chloromethylpyridinium chloride

: 1616474-18-0
N-(2-(piperidin-1-yl)ethyl)-2-(3-((4-(3-(pyridin-3-ylmethoxy)phenyl)-7-tosyl-7H-pyrrolo[2,3-d]pyrimidin-2-yl)amino)phenyl)acetamide

Guidance literature:: Multi-step reaction with 4 steps

1: caesium carbonate / N,N-dimethyl-formamide / 48 h / 20 - 80 °C

2: (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; potassium acetate / dimethyl sulfoxide / 16 h / 80 °C / Inert atmosphere

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

4: XPhos; tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; potassium carbonate / tert-butyl alcohol / 16 h / Inert atmosphere; Reflux

With (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; tetrakis(triphenylphosphine) palladium⁽⁰⁾; potassium acetate; sodium carbonate; potassium carbonate; caesium carbonate; XPhos; In 1,4-dioxane; water; dimethyl sulfoxide; N,N-dimethyl-formamide; tert-butyl alcohol; 2: |Miyaura Borylation Reaction / 3: |Suzuki Coupling / 4: |Buchwald-Hartwig Coupling;
DOI:10.1016/j.tet.2014.05.033

Reference yield:

: 1616474-10-2
2-(3-nitrophenyl)-N-(2-(piperidin-1-yl)ethyl)acetamide

: 1616474-18-0
N-(2-(piperidin-1-yl)ethyl)-2-(3-((4-(3-(pyridin-3-ylmethoxy)phenyl)-7-tosyl-7H-pyrrolo[2,3-d]pyrimidin-2-yl)amino)phenyl)acetamide

Guidance literature:: Multi-step reaction with 2 steps

1: 5%-palladium/activated carbon; hydrogen / methanol / 4 h / 20 °C / 760.05 Torr

2: XPhos; tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; potassium carbonate / tert-butyl alcohol / 16 h / Inert atmosphere; Reflux

With tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; 5%-palladium/activated carbon; hydrogen; potassium carbonate; XPhos; In methanol; tert-butyl alcohol; 2: |Buchwald-Hartwig Coupling;
DOI:10.1016/j.tet.2014.05.033