4-(((3-amino-2-methylphenyl)(4-(3-((tetrahydrofuran-3-yl)methoxy)phenoxy)benzyl)amino)methyl)benzonitrile

Base Information

Chemical Name:4-(((3-amino-2-methylphenyl)(4-(3-((tetrahydrofuran-3-yl)methoxy)phenoxy)benzyl)amino)methyl)benzonitrile
CAS No.:1264836-21-6
Molecular Formula:C₃₃H₃₃N₃O₃
Molecular Weight:519.643
Hs Code.:

Synonyms:4-(((3-amino-2-methylphenyl)(4-(3-((tetrahydrofuran-3-yl)methoxy)phenoxy)benzyl)amino)methyl)benzonitrile

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Chemical Property of 4-(((3-amino-2-methylphenyl)(4-(3-((tetrahydrofuran-3-yl)methoxy)phenoxy)benzyl)amino)methyl)benzonitrile

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Technology Process of 4-(((3-amino-2-methylphenyl)(4-(3-((tetrahydrofuran-3-yl)methoxy)phenoxy)benzyl)amino)methyl)benzonitrile

There total 5 articles about 4-(((3-amino-2-methylphenyl)(4-(3-((tetrahydrofuran-3-yl)methoxy)phenoxy)benzyl)amino)methyl)benzonitrile 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: 70.0%

: 1264836-20-5
4-(((2-methyl-3-nitrophenyl)(4-(3-((tetrahydrofuran-3-yl)methoxy)phenoxy)benzyl)amino)methyl)benzonitrile

: 1264836-21-6
4-(((3-amino-2-methylphenyl)(4-(3-((tetrahydrofuran-3-yl)methoxy)phenoxy)benzyl)amino)methyl)benzonitrile

Guidance literature:: With iron; ammonium chloride; In ethanol; water; for 2h; Reflux;

Reference yield:

: 17201-43-3
4-cyanobenzyl bromide

: 1264836-21-6
4-(((3-amino-2-methylphenyl)(4-(3-((tetrahydrofuran-3-yl)methoxy)phenoxy)benzyl)amino)methyl)benzonitrile

Guidance literature:: Multi-step reaction with 4 steps

1: N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide / 40 h / 90 - 100 °C / Inert atmosphere

2: potassium carbonate; methanol / tetrakis(triphenylphosphine) palladium⁽⁰⁾ / 3 h / 50 - 60 °C / Inert atmosphere

3: caesium carbonate / tetrabutylammomium bromide / N,N-dimethyl-formamide / 2 h / 100 - 110 °C

4: ammonium chloride; iron / ethanol; water / 2 h / Reflux

With methanol; iron; potassium carbonate; ammonium chloride; caesium carbonate; N-ethyl-N,N-diisopropylamine; tetrakis(triphenylphosphine) palladium⁽⁰⁾; tetrabutylammomium bromide; In ethanol; water; N,N-dimethyl-formamide;

Reference yield:

: N-{4-[3-(allyloxy)phenoxy]benzyl}-N-(2-methyl-3-nitrophenyl)amine

: 1264836-21-6
4-(((3-amino-2-methylphenyl)(4-(3-((tetrahydrofuran-3-yl)methoxy)phenoxy)benzyl)amino)methyl)benzonitrile

Guidance literature:: Multi-step reaction with 4 steps

1: N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide / 40 h / 90 - 100 °C / Inert atmosphere

2: potassium carbonate; methanol / tetrakis(triphenylphosphine) palladium⁽⁰⁾ / 3 h / 50 - 60 °C / Inert atmosphere

3: caesium carbonate / tetrabutylammomium bromide / N,N-dimethyl-formamide / 2 h / 100 - 110 °C

4: ammonium chloride; iron / ethanol; water / 2 h / Reflux

With methanol; iron; potassium carbonate; ammonium chloride; caesium carbonate; N-ethyl-N,N-diisopropylamine; tetrakis(triphenylphosphine) palladium⁽⁰⁾; tetrabutylammomium bromide; In ethanol; water; N,N-dimethyl-formamide;