3-amino-4'-(7-chloroquinolin-4-ylamino)-4-nitrodiphenyl ether hydrochloride

Base Information

Chemical Name:3-amino-4'-(7-chloroquinolin-4-ylamino)-4-nitrodiphenyl ether hydrochloride
CAS No.:103248-67-5
Molecular Formula:C₂₁H₁₅ClN₄O₃*ClH
Molecular Weight:443.289
Hs Code.:

Synonyms:3-amino-4'-(7-chloroquinolin-4-ylamino)-4-nitrodiphenyl ether hydrochloride

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Chemical Property of 3-amino-4'-(7-chloroquinolin-4-ylamino)-4-nitrodiphenyl ether hydrochloride

Chemical Property:

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Technology Process of 3-amino-4'-(7-chloroquinolin-4-ylamino)-4-nitrodiphenyl ether hydrochloride

There total 3 articles about 3-amino-4'-(7-chloroquinolin-4-ylamino)-4-nitrodiphenyl ether hydrochloride 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:

: 1635-61-6
5-chloro-2-nitroaniline

: 103248-67-5
3-amino-4'-(7-chloroquinolin-4-ylamino)-4-nitrodiphenyl ether hydrochloride

Guidance literature:: Multi-step reaction with 3 steps

1: 44 percent / dimethylformamide / 24 h / Heating

2: 85 percent / conc. HCl / 2 h / Heating

3: 80 percent / ethanol / 5 h / Heating

With hydrogenchloride; In ethanol; N,N-dimethyl-formamide;

Reference yield:

: 29178-59-4
4-(4-acetylaminophenoxy)-2-amino-nitrobenzene

: 103248-67-5
3-amino-4'-(7-chloroquinolin-4-ylamino)-4-nitrodiphenyl ether hydrochloride

Guidance literature:: Multi-step reaction with 2 steps

1: 85 percent / conc. HCl / 2 h / Heating

2: 80 percent / ethanol / 5 h / Heating

With hydrogenchloride; In ethanol;

Reference yield:

: 35719-43-8
potassium salt of 4-acetamidophenol

: 103248-67-5
3-amino-4'-(7-chloroquinolin-4-ylamino)-4-nitrodiphenyl ether hydrochloride

Guidance literature:: Multi-step reaction with 3 steps

1: 44 percent / dimethylformamide / 24 h / Heating

2: 85 percent / conc. HCl / 2 h / Heating

3: 80 percent / ethanol / 5 h / Heating

With hydrogenchloride; In ethanol; N,N-dimethyl-formamide;