N-(5-tert-butyl-3-methanesulphonylamino-2-methoxy-phenyl)-4-chloro-3-[2-(1-methyl-piperidin-4-ylamino)-pyridin-4-yloxy]-benzamide

Base Information

Chemical Name:N-(5-tert-butyl-3-methanesulphonylamino-2-methoxy-phenyl)-4-chloro-3-[2-(1-methyl-piperidin-4-ylamino)-pyridin-4-yloxy]-benzamide
CAS No.:1215029-46-1
Molecular Formula:C₃₀H₃₈ClN₅O₅S
Molecular Weight:616.181
Hs Code.:

Synonyms:N-(5-tert-butyl-3-methanesulphonylamino-2-methoxy-phenyl)-4-chloro-3-[2-(1-methyl-piperidin-4-ylamino)-pyridin-4-yloxy]-benzamide

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Chemical Property of N-(5-tert-butyl-3-methanesulphonylamino-2-methoxy-phenyl)-4-chloro-3-[2-(1-methyl-piperidin-4-ylamino)-pyridin-4-yloxy]-benzamide

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Technology Process of N-(5-tert-butyl-3-methanesulphonylamino-2-methoxy-phenyl)-4-chloro-3-[2-(1-methyl-piperidin-4-ylamino)-pyridin-4-yloxy]-benzamide

There total 3 articles about N-(5-tert-butyl-3-methanesulphonylamino-2-methoxy-phenyl)-4-chloro-3-[2-(1-methyl-piperidin-4-ylamino)-pyridin-4-yloxy]-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: 5.0%

: 41838-46-4
4-Amino-1-methylpiperidine

: 1215030-53-7
N-(5-tert-butyl-3-methanesulphonylamino-2-methoxy-phenyl)-4-chloro-3-(2-chloro-pyridin-4-yloxy)-benzamide

: 1215029-46-1
N-(5-tert-butyl-3-methanesulphonylamino-2-methoxy-phenyl)-4-chloro-3-[2-(1-methyl-piperidin-4-ylamino)-pyridin-4-yloxy]-benzamide

Guidance literature:: With potassium tert-butylate; tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; 2,8,9-tris(2-methylpropyl)-2,5,8,9-tetraaza-1-phosphabicyclo[3.3.3]undecane; In toluene; at 105 ℃; Inert atmosphere;

Reference yield:

: 34941-91-8
2-chloro-4-fluoropyridine

: 1215029-46-1
N-(5-tert-butyl-3-methanesulphonylamino-2-methoxy-phenyl)-4-chloro-3-[2-(1-methyl-piperidin-4-ylamino)-pyridin-4-yloxy]-benzamide

Guidance literature:: Multi-step reaction with 2 steps

1: potassium carbonate / dimethyl sulfoxide / 50 °C

2: potassium tert-butylate / tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; 2,8,9-tris(2-methylpropyl)-2,5,8,9-tetraaza-1-phosphabicyclo[3.3.3]undecane / toluene / 105 °C / Inert atmosphere

With potassium tert-butylate; potassium carbonate; tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; 2,8,9-tris(2-methylpropyl)-2,5,8,9-tetraaza-1-phosphabicyclo[3.3.3]undecane; In dimethyl sulfoxide; toluene;

Reference yield:

: 1215030-20-8
N-(5-tert-butyl-3-methanesulphonylamino-2-methoxy-phenyl)-3-hydroxy-4-chloro-benzamide

: 1215029-46-1
N-(5-tert-butyl-3-methanesulphonylamino-2-methoxy-phenyl)-4-chloro-3-[2-(1-methyl-piperidin-4-ylamino)-pyridin-4-yloxy]-benzamide

Guidance literature:: Multi-step reaction with 2 steps

1: potassium carbonate / dimethyl sulfoxide / 50 °C

2: potassium tert-butylate / tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; 2,8,9-tris(2-methylpropyl)-2,5,8,9-tetraaza-1-phosphabicyclo[3.3.3]undecane / toluene / 105 °C / Inert atmosphere

With potassium tert-butylate; potassium carbonate; tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; 2,8,9-tris(2-methylpropyl)-2,5,8,9-tetraaza-1-phosphabicyclo[3.3.3]undecane; In dimethyl sulfoxide; toluene;