Tert-butyl 4-{4-[5-(5-tert-butyl-3-methanesulphonylamino-2-methoxy-phenylcarbamoyl)-2-chloro-phenoxy]-pyridin-2-ylamino}-piperidine-1-carboxylate

Base Information

Chemical Name:Tert-butyl 4-{4-[5-(5-tert-butyl-3-methanesulphonylamino-2-methoxy-phenylcarbamoyl)-2-chloro-phenoxy]-pyridin-2-ylamino}-piperidine-1-carboxylate
CAS No.:1215031-52-9
Molecular Formula:C₃₄H₄₄ClN₅O₇S
Molecular Weight:702.272
Hs Code.:

Tert-butyl 4-{4-[5-(5-tert-butyl-3-methanesulphonylamino-2-methoxy-phenylcarbamoyl)-2-chloro-phenoxy]-pyridin-2-ylamino}-piperidine-1-carboxylate

Synonyms:Tert-butyl 4-{4-[5-(5-tert-butyl-3-methanesulphonylamino-2-methoxy-phenylcarbamoyl)-2-chloro-phenoxy]-pyridin-2-ylamino}-piperidine-1-carboxylate

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Chemical Property of Tert-butyl 4-{4-[5-(5-tert-butyl-3-methanesulphonylamino-2-methoxy-phenylcarbamoyl)-2-chloro-phenoxy]-pyridin-2-ylamino}-piperidine-1-carboxylate

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Technology Process of Tert-butyl 4-{4-[5-(5-tert-butyl-3-methanesulphonylamino-2-methoxy-phenylcarbamoyl)-2-chloro-phenoxy]-pyridin-2-ylamino}-piperidine-1-carboxylate

There total 3 articles about Tert-butyl 4-{4-[5-(5-tert-butyl-3-methanesulphonylamino-2-methoxy-phenylcarbamoyl)-2-chloro-phenoxy]-pyridin-2-ylamino}-piperidine-1-carboxylate 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: 8.0%

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

: 87120-72-7
1-(tert-butoxycarbonyl)-4-aminopiperidine

: 1215031-52-9
Tert-butyl 4-{4-[5-(5-tert-butyl-3-methanesulphonylamino-2-methoxy-phenylcarbamoyl)-2-chloro-phenoxy]-pyridin-2-ylamino}-piperidine-1-carboxylate

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 150 ℃; for 40h; Inert atmosphere;

Reference yield:

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

: 1215031-52-9
Tert-butyl 4-{4-[5-(5-tert-butyl-3-methanesulphonylamino-2-methoxy-phenylcarbamoyl)-2-chloro-phenoxy]-pyridin-2-ylamino}-piperidine-1-carboxylate

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 / 40 h / 150 °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

: 1215031-52-9
Tert-butyl 4-{4-[5-(5-tert-butyl-3-methanesulphonylamino-2-methoxy-phenylcarbamoyl)-2-chloro-phenoxy]-pyridin-2-ylamino}-piperidine-1-carboxylate

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 / 40 h / 150 °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;