N-(4-(3-chloro-4-fluorophenyl))-7-(8-methyl-8-azabicyclo[3.2.1]octan-3-yloxy)-6-nitroquinazolin-4-amine

Base Information

Chemical Name:N-(4-(3-chloro-4-fluorophenyl))-7-(8-methyl-8-azabicyclo[3.2.1]octan-3-yloxy)-6-nitroquinazolin-4-amine
CAS No.:1363359-61-8
Molecular Formula:C₂₂H₂₁ClFN₅O₃
Molecular Weight:457.892
Hs Code.:

Synonyms:N-(4-(3-chloro-4-fluorophenyl))-7-(8-methyl-8-azabicyclo[3.2.1]octan-3-yloxy)-6-nitroquinazolin-4-amine

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Chemical Property of N-(4-(3-chloro-4-fluorophenyl))-7-(8-methyl-8-azabicyclo[3.2.1]octan-3-yloxy)-6-nitroquinazolin-4-amine

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Technology Process of N-(4-(3-chloro-4-fluorophenyl))-7-(8-methyl-8-azabicyclo[3.2.1]octan-3-yloxy)-6-nitroquinazolin-4-amine

There total 5 articles about N-(4-(3-chloro-4-fluorophenyl))-7-(8-methyl-8-azabicyclo[3.2.1]octan-3-yloxy)-6-nitroquinazolin-4-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: 37.0%

: 7432-10-2,911648-75-4
Tropanol

: 162012-67-1
N-(3-chloro-4-fluorophenyl)-7-fluoro-6-nitroquinazolin-4-amine

: 1363359-61-8
N-(4-(3-chloro-4-fluorophenyl))-7-(8-methyl-8-azabicyclo[3.2.1]octan-3-yloxy)-6-nitroquinazolin-4-amine

Guidance literature:: Tropanol; With sodium hydride; In N,N-dimethyl-formamide; mineral oil; at 20 ℃; for 1h; Inert atmosphere; Cooling with ice;

N-(3-chloro-4-fluorophenyl)-7-fluoro-6-nitroquinazolin-4-amine; In N,N-dimethyl-formamide; at 50 ℃;

Reference yield:

: 446-32-2
4-fluoroanthranilic acid

: 1363359-61-8
N-(4-(3-chloro-4-fluorophenyl))-7-(8-methyl-8-azabicyclo[3.2.1]octan-3-yloxy)-6-nitroquinazolin-4-amine

Guidance literature:: Multi-step reaction with 5 steps

1.1: acetic acid / 2-methoxy-ethanol / Reflux

2.1: nitric acid; sulfuric acid

3.1: thionyl chloride

4.1: isopropyl alcohol

5.1: sodium hydride / N,N-dimethyl-formamide; mineral oil / 1 h / 20 °C / Inert atmosphere; Cooling with ice

5.2: 50 °C

With thionyl chloride; sulfuric acid; nitric acid; sodium hydride; acetic acid; In 2-methoxy-ethanol; N,N-dimethyl-formamide; isopropyl alcohol; mineral oil;

Reference yield:

: 16499-57-3
7-fluoro-3H-quinazolin-4-one

: 1363359-61-8
N-(4-(3-chloro-4-fluorophenyl))-7-(8-methyl-8-azabicyclo[3.2.1]octan-3-yloxy)-6-nitroquinazolin-4-amine

Guidance literature:: Multi-step reaction with 4 steps

1.1: nitric acid; sulfuric acid

2.1: thionyl chloride

3.1: isopropyl alcohol

4.1: sodium hydride / N,N-dimethyl-formamide; mineral oil / 1 h / 20 °C / Inert atmosphere; Cooling with ice

4.2: 50 °C

With thionyl chloride; sulfuric acid; nitric acid; sodium hydride; In N,N-dimethyl-formamide; isopropyl alcohol; mineral oil;