8-((4-Amino-1-methylbutyl)amino)-6-methoxy-5-(4-methoxyphenoxy)-4-methyl-quinoline

Base Information

Chemical Name:8-((4-Amino-1-methylbutyl)amino)-6-methoxy-5-(4-methoxyphenoxy)-4-methyl-quinoline
CAS No.:80737-22-0
Molecular Formula:C₂₃H₂₉N₃O₃
Molecular Weight:395.502
Hs Code.:

Synonyms:8-((4-Amino-1-methylbutyl)amino)-6-methoxy-5-(4-methoxyphenoxy)-4-methyl-quinoline

Suppliers and Price of 8-((4-Amino-1-methylbutyl)amino)-6-methoxy-5-(4-methoxyphenoxy)-4-methyl-quinoline

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Chemical Property of 8-((4-Amino-1-methylbutyl)amino)-6-methoxy-5-(4-methoxyphenoxy)-4-methyl-quinoline

Chemical Property:

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Technology Process of 8-((4-Amino-1-methylbutyl)amino)-6-methoxy-5-(4-methoxyphenoxy)-4-methyl-quinoline

There total 7 articles about 8-((4-Amino-1-methylbutyl)amino)-6-methoxy-5-(4-methoxyphenoxy)-4-methyl-quinoline 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:

: 81358-92-1
5-chloro-6-methoxy-4-methyl-8-nitroquinoline

: 80737-22-0
8-((4-Amino-1-methylbutyl)amino)-6-methoxy-5-(4-methoxyphenoxy)-4-methyl-quinoline

Guidance literature:: Multi-step reaction with 4 steps

1: 68 percent / KOH / 2-ethoxy-ethanol / 8 h / Heating

2: 58 percent / H₂ / Raney Ni / ethanol; dioxane / 1.25 h / 2327.2 Torr

3: 71 percent / Et₃N / 2-ethoxy-ethanol / 6.5 h / 105 °C

4: hydrazine hydrate / ethanol / 6 h / Heating

With potassium hydroxide; hydrogen; hydrazine hydrate; triethylamine; nickel; In 1,4-dioxane; 2-ethoxy-ethanol; ethanol;
DOI:10.1021/jm00351a017

Reference yield:

: 81358-81-8
4-methyl-5-hydroxy-6-methoxy-8-nitroquinoline

: 80737-22-0
8-((4-Amino-1-methylbutyl)amino)-6-methoxy-5-(4-methoxyphenoxy)-4-methyl-quinoline

Guidance literature:: Multi-step reaction with 5 steps

1: 69 percent / POCl₃ / 2 h / 80 °C

2: 68 percent / KOH / 2-ethoxy-ethanol / 8 h / Heating

3: 58 percent / H₂ / Raney Ni / ethanol; dioxane / 1.25 h / 2327.2 Torr

4: 71 percent / Et₃N / 2-ethoxy-ethanol / 6.5 h / 105 °C

5: hydrazine hydrate / ethanol / 6 h / Heating

With potassium hydroxide; hydrogen; hydrazine hydrate; triethylamine; trichlorophosphate; nickel; In 1,4-dioxane; 2-ethoxy-ethanol; ethanol;
DOI:10.1021/jm00351a017

Reference yield:

: 82333-40-2
6-Methoxy-5-(4-methoxyphenoxy)-4-methyl-8-nitroquinoline

: 80737-22-0
8-((4-Amino-1-methylbutyl)amino)-6-methoxy-5-(4-methoxyphenoxy)-4-methyl-quinoline

Guidance literature:: Multi-step reaction with 3 steps

1: 58 percent / H₂ / Raney Ni / ethanol; dioxane / 1.25 h / 2327.2 Torr

2: 71 percent / Et₃N / 2-ethoxy-ethanol / 6.5 h / 105 °C

3: hydrazine hydrate / ethanol / 6 h / Heating

With hydrogen; hydrazine hydrate; triethylamine; nickel; In 1,4-dioxane; 2-ethoxy-ethanol; ethanol;
DOI:10.1021/jm00351a017