[2-(5-chloro-2-fluoro-phenyl)-quinolin-4-yl]-(3-nitro-pyridin-4-yl)-amine

Base Information

Chemical Name:[2-(5-chloro-2-fluoro-phenyl)-quinolin-4-yl]-(3-nitro-pyridin-4-yl)-amine
CAS No.:1303556-78-6
Molecular Formula:C₂₀H₁₂ClFN₄O₂
Molecular Weight:394.792
Hs Code.:

Synonyms:[2-(5-chloro-2-fluoro-phenyl)-quinolin-4-yl]-(3-nitro-pyridin-4-yl)-amine

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Chemical Property of [2-(5-chloro-2-fluoro-phenyl)-quinolin-4-yl]-(3-nitro-pyridin-4-yl)-amine

Chemical Property:

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Technology Process of [2-(5-chloro-2-fluoro-phenyl)-quinolin-4-yl]-(3-nitro-pyridin-4-yl)-amine

There total 5 articles about [2-(5-chloro-2-fluoro-phenyl)-quinolin-4-yl]-(3-nitro-pyridin-4-yl)-amine 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:

: 1303557-96-1
4-bromo-2-(5-chloro-2-fluoro-phenyl)-quinoline

: 1681-37-4
4-amino-3-nitropyridine

: 1303556-78-6
[2-(5-chloro-2-fluoro-phenyl)-quinolin-4-yl]-(3-nitro-pyridin-4-yl)-amine

Guidance literature:: With potassium phosphate; 4a,9a-dihydro-9,9-dimethyl-4,5-bis(diphenylphosphino)-xanthene; tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; In tert-Amyl alcohol; at 100 - 117 ℃; for 6.5h; Inert atmosphere;

Reference yield:

: 1019367-42-0
N-(2-acetyl-phenyl)-5-chloro-2-fluoro-benzamide

: 1303556-78-6
[2-(5-chloro-2-fluoro-phenyl)-quinolin-4-yl]-(3-nitro-pyridin-4-yl)-amine

Guidance literature:: Multi-step reaction with 3 steps

1.1: potassium tert-butylate / tert-butyl alcohol / 20 h / 75 °C

1.2: pH 1 - 2 / Cooling with ice

2.1: phosphorus(V) oxybromide / 1-methyl-pyrrolidin-2-one / 4.5 h / 20 - 95 °C

3.1: potassium phosphate; 4a,9a-dihydro-9,9-dimethyl-4,5-bis(diphenylphosphino)-xanthene / tris-(dibenzylideneacetone)dipalladium⁽⁰⁾ / tert-Amyl alcohol / 6.5 h / 100 - 117 °C / Inert atmosphere

With potassium phosphate; 4a,9a-dihydro-9,9-dimethyl-4,5-bis(diphenylphosphino)-xanthene; potassium tert-butylate; phosphorus(V) oxybromide; tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; In 1-methyl-pyrrolidin-2-one; tert-Amyl alcohol; tert-butyl alcohol;

Reference yield:

: 394-29-6
5-chloro-2-fluoro-benzoyl chloride

: 1303556-78-6
[2-(5-chloro-2-fluoro-phenyl)-quinolin-4-yl]-(3-nitro-pyridin-4-yl)-amine

Guidance literature:: Multi-step reaction with 4 steps

1.1: N-ethyl-N,N-diisopropylamine / tetrahydrofuran / 20 - 34 °C

2.1: potassium tert-butylate / tert-butyl alcohol / 20 h / 75 °C

2.2: pH 1 - 2 / Cooling with ice

3.1: phosphorus(V) oxybromide / 1-methyl-pyrrolidin-2-one / 4.5 h / 20 - 95 °C

4.1: potassium phosphate; 4a,9a-dihydro-9,9-dimethyl-4,5-bis(diphenylphosphino)-xanthene / tris-(dibenzylideneacetone)dipalladium⁽⁰⁾ / tert-Amyl alcohol / 6.5 h / 100 - 117 °C / Inert atmosphere

With potassium phosphate; 4a,9a-dihydro-9,9-dimethyl-4,5-bis(diphenylphosphino)-xanthene; potassium tert-butylate; N-ethyl-N,N-diisopropylamine; phosphorus(V) oxybromide; tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; In tetrahydrofuran; 1-methyl-pyrrolidin-2-one; tert-Amyl alcohol; tert-butyl alcohol;