tert-butyl 1-(4-(2-phenyl-1H-pyrrolo[3,2-c]pyridin-1-yl)phenyl)cyclobutylcarbamate

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Chemical Name:tert-butyl 1-(4-(2-phenyl-1H-pyrrolo[3,2-c]pyridin-1-yl)phenyl)cyclobutylcarbamate
CAS No.:1439394-37-2
Molecular Formula:C₂₈H₂₉N₃O₂
Molecular Weight:439.557
Hs Code.:

Synonyms:tert-butyl 1-(4-(2-phenyl-1H-pyrrolo[3,2-c]pyridin-1-yl)phenyl)cyclobutylcarbamate

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Chemical Property of tert-butyl 1-(4-(2-phenyl-1H-pyrrolo[3,2-c]pyridin-1-yl)phenyl)cyclobutylcarbamate

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Technology Process of tert-butyl 1-(4-(2-phenyl-1H-pyrrolo[3,2-c]pyridin-1-yl)phenyl)cyclobutylcarbamate

There total 3 articles about tert-butyl 1-(4-(2-phenyl-1H-pyrrolo[3,2-c]pyridin-1-yl)phenyl)cyclobutylcarbamate 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: 13.0%

: 1020536-57-5
4-chloro-3-(2-phenylethynyl)pyridine

: 1259224-00-4
[1-(4-amino-phenyl)-cyclobutyl]-carbamic acid tert-butyl ester

: 1439394-37-2
tert-butyl 1-(4-(2-phenyl-1H-pyrrolo[3,2-c]pyridin-1-yl)phenyl)cyclobutylcarbamate

Guidance literature:: With tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; caesium carbonate; XPhos; In 1,4-dioxane; at 120 ℃; for 1h; Inert atmosphere; Microwave irradiation;

Reference yield:

: 626-61-9
4-Chloropyridine

: 1439394-37-2
tert-butyl 1-(4-(2-phenyl-1H-pyrrolo[3,2-c]pyridin-1-yl)phenyl)cyclobutylcarbamate

Guidance literature:: Multi-step reaction with 3 steps

1.1: lithium diisopropyl amide / tetrahydrofuran; hexane / 0.5 h / -78 - -70 °C / Inert atmosphere

1.2: 2.67 h / -65 - 20 °C / Inert atmosphere

2.1: bis-triphenylphosphine-palladium(II) chloride; copper(l) iodide; triethylamine / 1 h / Inert atmosphere; Reflux

3.1: caesium carbonate; XPhos; tris-(dibenzylideneacetone)dipalladium⁽⁰⁾ / 1,4-dioxane / 1 h / 120 °C / Inert atmosphere; Microwave irradiation

With bis-triphenylphosphine-palladium(II) chloride; tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; copper(l) iodide; caesium carbonate; triethylamine; lithium diisopropyl amide; XPhos; In tetrahydrofuran; 1,4-dioxane; hexane;

Reference yield:

: 89167-34-0
4-chloro-3-iodopyridine

: 1439394-37-2
tert-butyl 1-(4-(2-phenyl-1H-pyrrolo[3,2-c]pyridin-1-yl)phenyl)cyclobutylcarbamate

Guidance literature:: Multi-step reaction with 2 steps

1: bis-triphenylphosphine-palladium(II) chloride; copper(l) iodide; triethylamine / 1 h / Inert atmosphere; Reflux

2: caesium carbonate; XPhos; tris-(dibenzylideneacetone)dipalladium⁽⁰⁾ / 1,4-dioxane / 1 h / 120 °C / Inert atmosphere; Microwave irradiation

With bis-triphenylphosphine-palladium(II) chloride; tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; copper(l) iodide; caesium carbonate; triethylamine; XPhos; In 1,4-dioxane;