methyl (3-(((4-(4-amino-2-(ethoxymethyl)-1H-imidazo[4,5-c]quinolin-1-yl)butyl)amino)methyl)phenyl)acetate

Base Information

Chemical Name:methyl (3-(((4-(4-amino-2-(ethoxymethyl)-1H-imidazo[4,5-c]quinolin-1-yl)butyl)amino)methyl)phenyl)acetate
CAS No.:1382350-80-2
Molecular Formula:C₂₇H₃₃N₅O₃
Molecular Weight:475.591
Hs Code.:

Synonyms:methyl (3-(((4-(4-amino-2-(ethoxymethyl)-1H-imidazo[4,5-c]quinolin-1-yl)butyl)amino)methyl)phenyl)acetate

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Chemical Property of methyl (3-(((4-(4-amino-2-(ethoxymethyl)-1H-imidazo[4,5-c]quinolin-1-yl)butyl)amino)methyl)phenyl)acetate

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Technology Process of methyl (3-(((4-(4-amino-2-(ethoxymethyl)-1H-imidazo[4,5-c]quinolin-1-yl)butyl)amino)methyl)phenyl)acetate

There total 5 articles about methyl (3-(((4-(4-amino-2-(ethoxymethyl)-1H-imidazo[4,5-c]quinolin-1-yl)butyl)amino)methyl)phenyl)acetate 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:

: 1-(4-aminobutyl)-2-(ethoxymethyl)-1H-imidazo[4,5-c]quinolin4-amine

: 142327-44-4
methyl 3-formylphenylacetate

: 1382350-80-2
methyl (3-(((4-(4-amino-2-(ethoxymethyl)-1H-imidazo[4,5-c]quinolin-1-yl)butyl)amino)methyl)phenyl)acetate

Guidance literature:: 1-(4-aminobutyl)-2-(ethoxymethyl)-1H-imidazo[4,5-c]quinolin4-amine; methyl 3-formylphenylacetate; With acetic acid; In methanol; at 20 ℃; for 0.333333h;

With sodium cyanoborohydride; In methanol; at 20 ℃; for 3h;

Reference yield:

: 50332-66-6
3-nitro-quinolin-4-ol

: 1382350-80-2
methyl (3-(((4-(4-amino-2-(ethoxymethyl)-1H-imidazo[4,5-c]quinolin-1-yl)butyl)amino)methyl)phenyl)acetate

Guidance literature:: Multi-step reaction with 5 steps

1.1: thionyl chloride / dichloromethane; N,N-dimethyl-formamide / 2 h / 40 °C

1.2: 2 h / 0 - 20 °C

2.1: sodium tetrahydroborate; nickel(II) chloride hexahydrate / methanol / 5 - 23 °C

3.1: triethylamine / dichloromethane / 0 °C / Reflux

4.1: hydrogenchloride / 1,4-dioxane; methanol / 3 h / 20 °C

5.1: acetic acid / methanol / 0.33 h / 20 °C

5.2: 3 h / 20 °C

With hydrogenchloride; sodium tetrahydroborate; thionyl chloride; nickel(II) chloride hexahydrate; acetic acid; triethylamine; In 1,4-dioxane; methanol; dichloromethane; N,N-dimethyl-formamide;

Reference yield:

: 210303-90-5
1,1-dimethylethyl N-{4-[(3-aminoquinolin-4-yl)amino]butyl}carbamate

: 1382350-80-2
methyl (3-(((4-(4-amino-2-(ethoxymethyl)-1H-imidazo[4,5-c]quinolin-1-yl)butyl)amino)methyl)phenyl)acetate

Guidance literature:: Multi-step reaction with 3 steps

1.1: triethylamine / dichloromethane / 0 °C / Reflux

2.1: hydrogenchloride / 1,4-dioxane; methanol / 3 h / 20 °C

3.1: acetic acid / methanol / 0.33 h / 20 °C

3.2: 3 h / 20 °C

With hydrogenchloride; acetic acid; triethylamine; In 1,4-dioxane; methanol; dichloromethane;