N-(3-(5-chloro-2-((3-morpholinophenyl)amino)-7-((2-(trimethylsilyl)ethoxy)methyl)-7H-pyrrolo[2,3-d]pyrimidin-4-yl)phenyl)acrylamide

Base Information

Chemical Name:N-(3-(5-chloro-2-((3-morpholinophenyl)amino)-7-((2-(trimethylsilyl)ethoxy)methyl)-7H-pyrrolo[2,3-d]pyrimidin-4-yl)phenyl)acrylamide
CAS No.:1594134-03-8
Molecular Formula:C₃₁H₃₇ClN₆O₃Si
Molecular Weight:605.212
Hs Code.:

Synonyms:N-(3-(5-chloro-2-((3-morpholinophenyl)amino)-7-((2-(trimethylsilyl)ethoxy)methyl)-7H-pyrrolo[2,3-d]pyrimidin-4-yl)phenyl)acrylamide

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Chemical Property of N-(3-(5-chloro-2-((3-morpholinophenyl)amino)-7-((2-(trimethylsilyl)ethoxy)methyl)-7H-pyrrolo[2,3-d]pyrimidin-4-yl)phenyl)acrylamide

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Technology Process of N-(3-(5-chloro-2-((3-morpholinophenyl)amino)-7-((2-(trimethylsilyl)ethoxy)methyl)-7H-pyrrolo[2,3-d]pyrimidin-4-yl)phenyl)acrylamide

There total 5 articles about N-(3-(5-chloro-2-((3-morpholinophenyl)amino)-7-((2-(trimethylsilyl)ethoxy)methyl)-7H-pyrrolo[2,3-d]pyrimidin-4-yl)phenyl)acrylamide 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: 17.92%

: 1594134-02-7
N-(3-(2-((3-morpholinophenyl)amino)-7-((2-(trimethylsilyl)ethoxy)methyl)-7H-pyrrolo[2,3-d]pyrimidin-4-yl)phenyl)acrylamide

: 1594134-03-8
N-(3-(5-chloro-2-((3-morpholinophenyl)amino)-7-((2-(trimethylsilyl)ethoxy)methyl)-7H-pyrrolo[2,3-d]pyrimidin-4-yl)phenyl)acrylamide

Guidance literature:: With N-chloro-succinimide; In dichloromethane; at 20 ℃;

Reference yield:

: 1594134-01-6
N-(3-(2-chloro-7-((2-(trimethylsilyl)ethoxy)methyl)-7H-pyrrolo[2,3-d]pyramidin-4-yl)phenyl)acrylamide

: 1594134-03-8
N-(3-(5-chloro-2-((3-morpholinophenyl)amino)-7-((2-(trimethylsilyl)ethoxy)methyl)-7H-pyrrolo[2,3-d]pyrimidin-4-yl)phenyl)acrylamide

Guidance literature:: Multi-step reaction with 2 steps

1: potassium carbonate; tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene / tert-butyl alcohol / 160 °C / Microwave irradiation

2: N-chloro-succinimide / dichloromethane / 20 °C

With tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; N-chloro-succinimide; potassium carbonate; 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene; In dichloromethane; tert-butyl alcohol;

Reference yield:

: 90213-66-4
2,4-dichloro-7H-pyrrolo[2,3-d]pyrimidine

: 1594134-03-8
N-(3-(5-chloro-2-((3-morpholinophenyl)amino)-7-((2-(trimethylsilyl)ethoxy)methyl)-7H-pyrrolo[2,3-d]pyrimidin-4-yl)phenyl)acrylamide

Guidance literature:: Multi-step reaction with 4 steps

1.1: sodium hydride / N,N-dimethyl-formamide / 0 - 20 °C

1.2: 20 °C

2.1: sodium carbonate; palladium diacetate; triphenylphosphine / tetrahydrofuran; water / 2 h / 150 °C / Microwave irradiation

3.1: potassium carbonate; tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene / tert-butyl alcohol / 160 °C / Microwave irradiation

4.1: N-chloro-succinimide / dichloromethane / 20 °C

With tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; N-chloro-succinimide; palladium diacetate; sodium hydride; sodium carbonate; potassium carbonate; triphenylphosphine; 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene; In tetrahydrofuran; dichloromethane; water; N,N-dimethyl-formamide; tert-butyl alcohol;