2-((5-chloro-2-((1-(2-oxo-2-(pyrrolidin-1-yl)-ethyl)pyrazol-4-yl)amino)-4-pyridyl)amino)-N-methyl-benzamide

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Chemical Name:2-((5-chloro-2-((1-(2-oxo-2-(pyrrolidin-1-yl)-ethyl)pyrazol-4-yl)amino)-4-pyridyl)amino)-N-methyl-benzamide
CAS No.:1201933-80-3
Molecular Formula:C₂₂H₂₄ClN₇O₂
Molecular Weight:453.931
Hs Code.:

Synonyms:2-((5-chloro-2-((1-(2-oxo-2-(pyrrolidin-1-yl)-ethyl)pyrazol-4-yl)amino)-4-pyridyl)amino)-N-methyl-benzamide

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Chemical Property of 2-((5-chloro-2-((1-(2-oxo-2-(pyrrolidin-1-yl)-ethyl)pyrazol-4-yl)amino)-4-pyridyl)amino)-N-methyl-benzamide

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Technology Process of 2-((5-chloro-2-((1-(2-oxo-2-(pyrrolidin-1-yl)-ethyl)pyrazol-4-yl)amino)-4-pyridyl)amino)-N-methyl-benzamide

There total 4 articles about 2-((5-chloro-2-((1-(2-oxo-2-(pyrrolidin-1-yl)-ethyl)pyrazol-4-yl)amino)-4-pyridyl)amino)-N-methyl-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: 21.0%

: 123-75-1
pyrrolidine

: 1201935-43-4
2-[4-[[5-chloro-4-[[2-(methylcarbamoyl)phenyl]amino]pyridin-2-yl]amino]pyrazol-1-yl]acetic acid

: 1201933-80-3
2-((5-chloro-2-((1-(2-oxo-2-(pyrrolidin-1-yl)-ethyl)pyrazol-4-yl)amino)-4-pyridyl)amino)-N-methyl-benzamide

Guidance literature:: With HATU; In N,N-dimethyl acetamide; at 22 ℃;

Reference yield:

: 16110-09-1
2,5 dichloropyridine

: 1201933-80-3
2-((5-chloro-2-((1-(2-oxo-2-(pyrrolidin-1-yl)-ethyl)pyrazol-4-yl)amino)-4-pyridyl)amino)-N-methyl-benzamide

Guidance literature:: Multi-step reaction with 4 steps

1.1: n-butyllithium; diisopropylamine / tetrahydrofuran; 2-Methylpentane / 1.5 h / -78 °C / Inert atmosphere

1.2: -78 °C / Inert atmosphere

2.1: caesium carbonate / palladium diacetate; 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene / 1,4-dioxane / 18 h / 80 °C / Inert atmosphere

3.1: sodium t-butanolate / tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene / 1,4-dioxane / 1 h / 150 °C / Inert atmosphere; Microwave irradiation

4.1: HATU / N,N-dimethyl acetamide / 22 °C

With n-butyllithium; caesium carbonate; diisopropylamine; HATU; sodium t-butanolate; tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; palladium diacetate; 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene; In tetrahydrofuran; 1,4-dioxane; 2-Methylpentane; N,N-dimethyl acetamide;

Reference yield:

: 1061358-83-5
2-[(2,5-dichloropyridin-4-yl)amino]-N-methylbenzamide

: 1201933-80-3
2-((5-chloro-2-((1-(2-oxo-2-(pyrrolidin-1-yl)-ethyl)pyrazol-4-yl)amino)-4-pyridyl)amino)-N-methyl-benzamide

Guidance literature:: Multi-step reaction with 2 steps

1: sodium t-butanolate / tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene / 1,4-dioxane / 1 h / 150 °C / Inert atmosphere; Microwave irradiation

2: HATU / N,N-dimethyl acetamide / 22 °C

With HATU; sodium t-butanolate; tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene; In 1,4-dioxane; N,N-dimethyl acetamide;