2-(4-(1-aminocyclobutyl)phenyl)-3-phenylbenzofuran-7-carbonitrile

Base Information

Chemical Name:2-(4-(1-aminocyclobutyl)phenyl)-3-phenylbenzofuran-7-carbonitrile
CAS No.:1301608-82-1
Molecular Formula:C₂₅H₂₀N₂O
Molecular Weight:364.447
Hs Code.:

Synonyms:2-(4-(1-aminocyclobutyl)phenyl)-3-phenylbenzofuran-7-carbonitrile

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Chemical Property of 2-(4-(1-aminocyclobutyl)phenyl)-3-phenylbenzofuran-7-carbonitrile

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Technology Process of 2-(4-(1-aminocyclobutyl)phenyl)-3-phenylbenzofuran-7-carbonitrile

There total 6 articles about 2-(4-(1-aminocyclobutyl)phenyl)-3-phenylbenzofuran-7-carbonitrile 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: 45.0%

: 1301610-52-5
tert-butyl (1-(4-(7-cyano-3-phenylbenzofuran-2-yl)phenyl)cyclobutyl)carbamate

: 1301608-82-1
2-(4-(1-aminocyclobutyl)phenyl)-3-phenylbenzofuran-7-carbonitrile

Guidance literature:: tert-butyl (1-(4-(7-cyano-3-phenylbenzofuran-2-yl)phenyl)cyclobutyl)carbamate; With hydrogenchloride; In tetrahydrofuran; 1,4-dioxane; at 20 ℃; for 16h;

With sodium hydrogencarbonate; In tetrahydrofuran; 1,4-dioxane; ethyl acetate;

Reference yield:

: 1032350-06-3
tert-butyl (1-(4-bromophenyl)cyclobutyl)carbamate

: 1301608-82-1
2-(4-(1-aminocyclobutyl)phenyl)-3-phenylbenzofuran-7-carbonitrile

Guidance literature:: Multi-step reaction with 6 steps

1: diisopropylamine / copper(l) iodide; bis(tri-t-butylphosphine)palladium⁽⁰⁾ / 1,4-dioxane / 20 h / 20 - 80 °C / Inert atmosphere

2: potassium carbonate; methanol / 1 h

3: triethylamine / copper(l) iodide; bis(tri-t-butylphosphine)palladium⁽⁰⁾ / 16 h / 0 - 20 °C

4: Iodine monochloride / dichloromethane / 3.08 h / 0 - 20 °C

5: cesium fluoride / triphenylphosphine; palladium diacetate / 1,2-dimethoxyethane / 16 h / 75 °C

6: hydrogenchloride / 1,4-dioxane; tetrahydrofuran / 16 h / 20 °C

With hydrogenchloride; methanol; Iodine monochloride; potassium carbonate; triethylamine; diisopropylamine; cesium fluoride; copper(l) iodide; bis(tri-t-butylphosphine)palladium⁽⁰⁾; palladium diacetate; triphenylphosphine; In tetrahydrofuran; 1,4-dioxane; 1,2-dimethoxyethane; dichloromethane;

Reference yield:

: 1301610-33-2
tert-butyl 1-(4-ethynylphenyl)cyclobutylcarbamate

: 1301608-82-1
2-(4-(1-aminocyclobutyl)phenyl)-3-phenylbenzofuran-7-carbonitrile

Guidance literature:: Multi-step reaction with 4 steps

1: triethylamine / copper(l) iodide; bis(tri-t-butylphosphine)palladium⁽⁰⁾ / 16 h / 0 - 20 °C

2: Iodine monochloride / dichloromethane / 3.08 h / 0 - 20 °C

3: cesium fluoride / triphenylphosphine; palladium diacetate / 1,2-dimethoxyethane / 16 h / 75 °C

4: hydrogenchloride / 1,4-dioxane; tetrahydrofuran / 16 h / 20 °C

With hydrogenchloride; Iodine monochloride; triethylamine; cesium fluoride; copper(l) iodide; bis(tri-t-butylphosphine)palladium⁽⁰⁾; palladium diacetate; triphenylphosphine; In tetrahydrofuran; 1,4-dioxane; 1,2-dimethoxyethane; dichloromethane;