4-{4-[2'-(5-chloro-2-fluoro-phenyl)-[3,4']bipyridinyl-5-yl]-pyrazol-1-yl}-piperidine-1-carboxylic acid tert-butyl ester

Base Information

Chemical Name:4-{4-[2'-(5-chloro-2-fluoro-phenyl)-[3,4']bipyridinyl-5-yl]-pyrazol-1-yl}-piperidine-1-carboxylic acid tert-butyl ester
CAS No.:1354758-84-1
Molecular Formula:C₂₉H₂₉ClFN₅O₂
Molecular Weight:534.033
Hs Code.:

Synonyms:4-{4-[2'-(5-chloro-2-fluoro-phenyl)-[3,4']bipyridinyl-5-yl]-pyrazol-1-yl}-piperidine-1-carboxylic acid tert-butyl ester

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Chemical Property of 4-{4-[2'-(5-chloro-2-fluoro-phenyl)-[3,4']bipyridinyl-5-yl]-pyrazol-1-yl}-piperidine-1-carboxylic acid tert-butyl ester

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Technology Process of 4-{4-[2'-(5-chloro-2-fluoro-phenyl)-[3,4']bipyridinyl-5-yl]-pyrazol-1-yl}-piperidine-1-carboxylic acid tert-butyl ester

There total 8 articles about 4-{4-[2'-(5-chloro-2-fluoro-phenyl)-[3,4']bipyridinyl-5-yl]-pyrazol-1-yl}-piperidine-1-carboxylic acid tert-butyl ester 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:

: 1323919-57-8
4-[4-(5-bromo-pyridin-3-yl)-pyrazol-1-yl]-piperidine-1-carboxylic acid tert-butyl-ester

: 1354758-81-8
2-(5-chloro-2-fluoro-phenyl)-pyridine-4-boronic acid

: 1354758-84-1
4-{4-[2'-(5-chloro-2-fluoro-phenyl)-[3,4']bipyridinyl-5-yl]-pyrazol-1-yl}-piperidine-1-carboxylic acid tert-butyl ester

Guidance literature:: With sodium hydrogencarbonate; bis-triphenylphosphine-palladium(II) chloride; In water; N,N-dimethyl-formamide; at 80 ℃; for 18h; Inert atmosphere;

Reference yield:

: 233770-01-9
3-bromo-5-iodopyridine

: 1354758-84-1
4-{4-[2'-(5-chloro-2-fluoro-phenyl)-[3,4']bipyridinyl-5-yl]-pyrazol-1-yl}-piperidine-1-carboxylic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: potassium phosphate tribasic trihydrate / bis-triphenylphosphine-palladium(II) chloride / 1,2-dimethoxyethane / 16 h / 80 °C / Inert atmosphere

2: sodium hydrogencarbonate / bis-triphenylphosphine-palladium(II) chloride / N,N-dimethyl-formamide; water / 18 h / 80 °C / Inert atmosphere

With potassium phosphate tribasic trihydrate; sodium hydrogencarbonate; bis-triphenylphosphine-palladium(II) chloride; In 1,2-dimethoxyethane; water; N,N-dimethyl-formamide;

Reference yield:

: 352535-83-2
5-chloro-2-fluorophenylboronic acid

: 1354758-84-1
4-{4-[2'-(5-chloro-2-fluoro-phenyl)-[3,4']bipyridinyl-5-yl]-pyrazol-1-yl}-piperidine-1-carboxylic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 5 steps

1.1: sodium hydrogencarbonate / bis-triphenylphosphine-palladium(II) chloride / N,N-dimethyl-formamide; water / 16 h / 80 °C / Inert atmosphere

2.1: hydrogenchloride / 1,4-dioxane; water; tetrahydrofuran

2.2: 24 h / 80 °C

2.3: 20 °C

3.1: potassium acetate / bis-triphenylphosphine-palladium(II) chloride / tetrahydrofuran / 24 h / 80 °C / Inert atmosphere

4.1: hydrogenchloride; water / tetrahydrofuran / 5 h / 20 °C / Inert atmosphere

5.1: sodium hydrogencarbonate / bis-triphenylphosphine-palladium(II) chloride / N,N-dimethyl-formamide; water / 18 h / 80 °C / Inert atmosphere

With hydrogenchloride; water; potassium acetate; sodium hydrogencarbonate; bis-triphenylphosphine-palladium(II) chloride; In tetrahydrofuran; 1,4-dioxane; water; N,N-dimethyl-formamide;