2-((2-((5-acrylamido-2-methoxyphenyl)amino)-5-chloro-7-((2-(trimethylsilyl)ethoxy)methyl)-7H-pyrrolo[2,3-d]pyrimidin-4-yl)amino)-N-methylbenzamide

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Chemical Name:2-((2-((5-acrylamido-2-methoxyphenyl)amino)-5-chloro-7-((2-(trimethylsilyl)ethoxy)methyl)-7H-pyrrolo[2,3-d]pyrimidin-4-yl)amino)-N-methylbenzamide
CAS No.:1346448-10-9
Molecular Formula:C₃₀H₃₆ClN₇O₄Si
Molecular Weight:622.199
Hs Code.:

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

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

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

There total 8 articles about 2-((2-((5-acrylamido-2-methoxyphenyl)amino)-5-chloro-7-((2-(trimethylsilyl)ethoxy)methyl)-7H-pyrrolo[2,3-d]pyrimidin-4-yl)amino)-N-methylbenzamide 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: 86.0%

: 1346448-09-6
2-((2-((5-amino-2-methoxyphenyl)amino)-5-chloro-7-((2-(trimethyl-silyl)ethoxy)methyl)-7H-pyrrolo[2,3-d]pyrimidin-4-yl)amino)-N-methylbenzamide

: 814-68-6,25189-84-8
acryloyl chloride

: 1346448-10-9
2-((2-((5-acrylamido-2-methoxyphenyl)amino)-5-chloro-7-((2-(trimethylsilyl)ethoxy)methyl)-7H-pyrrolo[2,3-d]pyrimidin-4-yl)amino)-N-methylbenzamide

Guidance literature:: With N-ethyl-N,N-diisopropylamine; In dichloromethane; at 0 ℃; for 0.0333333h;

Reference yield:

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

: 1346448-10-9
2-((2-((5-acrylamido-2-methoxyphenyl)amino)-5-chloro-7-((2-(trimethylsilyl)ethoxy)methyl)-7H-pyrrolo[2,3-d]pyrimidin-4-yl)amino)-N-methylbenzamide

Guidance literature:: Multi-step reaction with 6 steps

1.1: N-chloro-succinimide / N,N-dimethyl-formamide / 48 h / 20 °C

2.1: sodium hydride / N,N-dimethyl-formamide

2.2: 1 h / 0 - 20 °C

3.1: potassium tert-butylate / N,N-dimethyl-formamide / 1.5 h / 20 °C

4.1: potassium carbonate / tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; XPhos / tert-butyl alcohol / 14 h / 85 °C

5.1: ammonium chloride; iron / ethanol; water / 0.5 h / 90 °C

6.1: N-ethyl-N,N-diisopropylamine / dichloromethane / 0.03 h / 0 °C

With N-chloro-succinimide; potassium tert-butylate; iron; sodium hydride; potassium carbonate; ammonium chloride; N-ethyl-N,N-diisopropylamine; tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; XPhos; In ethanol; dichloromethane; water; N,N-dimethyl-formamide; tert-butyl alcohol;

Reference yield:

: 118-48-9
isatoic anhydride

: 1346448-10-9
2-((2-((5-acrylamido-2-methoxyphenyl)amino)-5-chloro-7-((2-(trimethylsilyl)ethoxy)methyl)-7H-pyrrolo[2,3-d]pyrimidin-4-yl)amino)-N-methylbenzamide

Guidance literature:: Multi-step reaction with 5 steps

1: 1,4-dioxane / 0.33 h

2: potassium tert-butylate / N,N-dimethyl-formamide / 1.5 h / 20 °C

3: potassium carbonate / tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; XPhos / tert-butyl alcohol / 14 h / 85 °C

4: ammonium chloride; iron / ethanol; water / 0.5 h / 90 °C

5: N-ethyl-N,N-diisopropylamine / dichloromethane / 0.03 h / 0 °C

With potassium tert-butylate; iron; potassium carbonate; ammonium chloride; N-ethyl-N,N-diisopropylamine; tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; XPhos; In 1,4-dioxane; ethanol; dichloromethane; water; N,N-dimethyl-formamide; tert-butyl alcohol;