N-(4-((2-amino-3-chloropyridin-4-yl)oxy)-3-fluorophenyl)-1-(4-fluorophenyl)-2-oxopiperidine-3-carboxamide

Base Information

Chemical Name:N-(4-((2-amino-3-chloropyridin-4-yl)oxy)-3-fluorophenyl)-1-(4-fluorophenyl)-2-oxopiperidine-3-carboxamide
CAS No.:1612842-46-2
Molecular Formula:C₂₃H₁₉ClF₂N₄O₃
Molecular Weight:472.879
Hs Code.:

Synonyms:N-(4-((2-amino-3-chloropyridin-4-yl)oxy)-3-fluorophenyl)-1-(4-fluorophenyl)-2-oxopiperidine-3-carboxamide

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Chemical Property of N-(4-((2-amino-3-chloropyridin-4-yl)oxy)-3-fluorophenyl)-1-(4-fluorophenyl)-2-oxopiperidine-3-carboxamide

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Technology Process of N-(4-((2-amino-3-chloropyridin-4-yl)oxy)-3-fluorophenyl)-1-(4-fluorophenyl)-2-oxopiperidine-3-carboxamide

There total 9 articles about N-(4-((2-amino-3-chloropyridin-4-yl)oxy)-3-fluorophenyl)-1-(4-fluorophenyl)-2-oxopiperidine-3-carboxamide 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: 72.0%

: 1612842-41-7
3-chloro-4-(2-fluoro-4-(1-(4-fluorophenyl)-2-oxopiperidine-3-carboxamido)phenoxy)picolinamide

: 1612842-46-2
N-(4-((2-amino-3-chloropyridin-4-yl)oxy)-3-fluorophenyl)-1-(4-fluorophenyl)-2-oxopiperidine-3-carboxamide

Guidance literature:: With [bis(acetoxy)iodo]benzene; In water; ethyl acetate; acetonitrile; at 0 - 20 ℃; for 2h;
DOI:10.3390/molecules19022655

Reference yield:

: 675-20-7
piperidin-2-one

: 1612842-46-2
N-(4-((2-amino-3-chloropyridin-4-yl)oxy)-3-fluorophenyl)-1-(4-fluorophenyl)-2-oxopiperidine-3-carboxamide

Guidance literature:: Multi-step reaction with 5 steps

1.1: potassium phosphate; copper(l) iodide / N,N-dimethyl-formamide / 12 h / 100 °C / Inert atmosphere

2.1: tert.-butyl lithium / tetrahydrofuran / 4 h / -78 °C / Inert atmosphere

2.2: 0.17 h / Inert atmosphere

3.1: lithium hydroxide monohydrate / tetrahydrofuran; methanol; water / 5 h / 0 - 20 °C / Inert atmosphere

4.1: 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; dmap / tetrahydrofuran / 0 - 20 °C / Inert atmosphere

5.1: [bis(acetoxy)iodo]benzene / water; ethyl acetate; acetonitrile / 2 h / 0 - 20 °C

With dmap; potassium phosphate; copper(l) iodide; lithium hydroxide monohydrate; [bis(acetoxy)iodo]benzene; tert.-butyl lithium; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In tetrahydrofuran; methanol; water; ethyl acetate; N,N-dimethyl-formamide; acetonitrile;
DOI:10.3390/molecules19022655

Reference yield:

: 352-34-1
4-fluoro-1-iodobenzene

: 1612842-46-2
N-(4-((2-amino-3-chloropyridin-4-yl)oxy)-3-fluorophenyl)-1-(4-fluorophenyl)-2-oxopiperidine-3-carboxamide

Guidance literature:: Multi-step reaction with 5 steps

1.1: potassium phosphate; copper(l) iodide / N,N-dimethyl-formamide / 12 h / 100 °C / Inert atmosphere

2.1: tert.-butyl lithium / tetrahydrofuran / 4 h / -78 °C / Inert atmosphere

2.2: 0.17 h / Inert atmosphere

3.1: lithium hydroxide monohydrate / tetrahydrofuran; methanol; water / 5 h / 0 - 20 °C / Inert atmosphere

4.1: 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; dmap / tetrahydrofuran / 0 - 20 °C / Inert atmosphere

5.1: [bis(acetoxy)iodo]benzene / water; ethyl acetate; acetonitrile / 2 h / 0 - 20 °C

With dmap; potassium phosphate; copper(l) iodide; lithium hydroxide monohydrate; [bis(acetoxy)iodo]benzene; tert.-butyl lithium; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In tetrahydrofuran; methanol; water; ethyl acetate; N,N-dimethyl-formamide; acetonitrile;
DOI:10.3390/molecules19022655