1-(4-amino-5-(3-fluorophenyl)-3-nitropyridin-2-yl)piperidine-3-carboxamide

Base Information

Chemical Name:1-(4-amino-5-(3-fluorophenyl)-3-nitropyridin-2-yl)piperidine-3-carboxamide
CAS No.:1600524-50-2
Molecular Formula:C₁₇H₁₈FN₅O₃
Molecular Weight:359.36
Hs Code.:

Synonyms:1-(4-amino-5-(3-fluorophenyl)-3-nitropyridin-2-yl)piperidine-3-carboxamide

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Chemical Property of 1-(4-amino-5-(3-fluorophenyl)-3-nitropyridin-2-yl)piperidine-3-carboxamide

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Technology Process of 1-(4-amino-5-(3-fluorophenyl)-3-nitropyridin-2-yl)piperidine-3-carboxamide

There total 5 articles about 1-(4-amino-5-(3-fluorophenyl)-3-nitropyridin-2-yl)piperidine-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: 80.0%

: 1600524-48-8
1-(4-Amino-5-iodo-3-nitropyridin-2-yl)piperidine-3-carboxamide

: 768-35-4
3-fluorophenylboronic acid

: 1600524-50-2
1-(4-amino-5-(3-fluorophenyl)-3-nitropyridin-2-yl)piperidine-3-carboxamide

Guidance literature:: With dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH₂Cl₂; potassium carbonate; In 1,2-dimethoxyethane; water; at 120 ℃; for 3h; Inert atmosphere; Schlenk technique; Sealed tube;
DOI:10.1016/j.ejmech.2014.03.019

Reference yield:

: 800402-12-4
2-chloro-4-amino-5-iodopyridine

: 1600524-50-2
1-(4-amino-5-(3-fluorophenyl)-3-nitropyridin-2-yl)piperidine-3-carboxamide

Guidance literature:: Multi-step reaction with 3 steps

1: sulfuric acid; nitric acid / 4 h / 20 °C / Cooling with ice

2: 1,4-dioxane; water / 6 h / 120 °C / Inert atmosphere; Sealed tube

3: potassium carbonate; dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH₂Cl₂ / water; 1,2-dimethoxyethane / 3 h / 120 °C / Inert atmosphere; Schlenk technique; Sealed tube

With dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH₂Cl₂; sulfuric acid; nitric acid; potassium carbonate; In 1,4-dioxane; 1,2-dimethoxyethane; water; 3: |Suzuki Coupling;
DOI:10.1016/j.ejmech.2014.03.019

Reference yield:

: 1600524-47-7
2-chloro-5-iodo-3-nitropyridin-4-amine

: 1600524-50-2
1-(4-amino-5-(3-fluorophenyl)-3-nitropyridin-2-yl)piperidine-3-carboxamide

Guidance literature:: Multi-step reaction with 2 steps

1: 1,4-dioxane; water / 6 h / 120 °C / Inert atmosphere; Sealed tube

2: potassium carbonate; dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH₂Cl₂ / water; 1,2-dimethoxyethane / 3 h / 120 °C / Inert atmosphere; Schlenk technique; Sealed tube

With dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH₂Cl₂; potassium carbonate; In 1,4-dioxane; 1,2-dimethoxyethane; water; 2: |Suzuki Coupling;
DOI:10.1016/j.ejmech.2014.03.019