1-(2-(4-((3,4-dichlorobenzyl)amino)piperidin-1-yl)ethyl)-7-methoxy-1,5-naphthyridin-2(1H)-one

Base Information

Chemical Name:1-(2-(4-((3,4-dichlorobenzyl)amino)piperidin-1-yl)ethyl)-7-methoxy-1,5-naphthyridin-2(1H)-one
CAS No.:1173896-46-2
Molecular Formula:C₂₃H₂₆Cl₂N₄O₂
Molecular Weight:461.391
Hs Code.:

Synonyms:1-(2-(4-((3,4-dichlorobenzyl)amino)piperidin-1-yl)ethyl)-7-methoxy-1,5-naphthyridin-2(1H)-one

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Chemical Property of 1-(2-(4-((3,4-dichlorobenzyl)amino)piperidin-1-yl)ethyl)-7-methoxy-1,5-naphthyridin-2(1H)-one

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Technology Process of 1-(2-(4-((3,4-dichlorobenzyl)amino)piperidin-1-yl)ethyl)-7-methoxy-1,5-naphthyridin-2(1H)-one

There total 9 articles about 1-(2-(4-((3,4-dichlorobenzyl)amino)piperidin-1-yl)ethyl)-7-methoxy-1,5-naphthyridin-2(1H)-one 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:

: 959615-59-9
7-methoxy-1,5-naphthyridin-2(1H)-one

: 1173896-46-2
1-(2-(4-((3,4-dichlorobenzyl)amino)piperidin-1-yl)ethyl)-7-methoxy-1,5-naphthyridin-2(1H)-one

Guidance literature:: Multi-step reaction with 6 steps

1.1: sodium hydride / 1,2-dimethoxyethane; N,N-dimethyl-formamide; mineral oil / 0.75 h / 0 °C / Inert atmosphere

1.2: 0.5 h / 20 °C / Inert atmosphere

1.3: 75 °C / Inert atmosphere

2.1: sodium periodate; osmium(VIII) oxide / water; 1,4-dioxane / 6 h / 20 °C

3.1: methanol; dichloromethane / 1 h

3.2: 1 h

4.1: hydrogenchloride / dichloromethane; 1,4-dioxane

5.1: triethylamine / methanol; dichloromethane / 0.25 h / 20 °C

5.2: 0.5 h / 20 °C

6.1: sodium tris(acetoxy)borohydride / methanol; dichloromethane

With hydrogenchloride; sodium periodate; osmium(VIII) oxide; sodium tris(acetoxy)borohydride; sodium hydride; triethylamine; In 1,4-dioxane; methanol; 1,2-dimethoxyethane; dichloromethane; water; N,N-dimethyl-formamide; mineral oil;
DOI:10.1128/AAC.03913-14

Reference yield:

: 1-(2-(4-aminopiperidin-1-yl)ethyl)-7-methoxy-1,5-naphthyridin-2(1H)-one dihydrochloride

: 1173896-46-2
1-(2-(4-((3,4-dichlorobenzyl)amino)piperidin-1-yl)ethyl)-7-methoxy-1,5-naphthyridin-2(1H)-one

Guidance literature:: Multi-step reaction with 2 steps

1.1: triethylamine / methanol; dichloromethane / 0.25 h / 20 °C

1.2: 0.5 h / 20 °C

2.1: sodium tris(acetoxy)borohydride / methanol; dichloromethane

With sodium tris(acetoxy)borohydride; triethylamine; In methanol; dichloromethane;
DOI:10.1128/AAC.03913-14

Reference yield:

: 959615-61-3
2-(7-methoxy-2-oxo-1,2-dihydro-1,5-naphthyridin-1-yl)acetaldehyde

: 1173896-46-2
1-(2-(4-((3,4-dichlorobenzyl)amino)piperidin-1-yl)ethyl)-7-methoxy-1,5-naphthyridin-2(1H)-one

Guidance literature:: Multi-step reaction with 4 steps

1.1: methanol; dichloromethane / 1 h

1.2: 1 h

2.1: hydrogenchloride / dichloromethane; 1,4-dioxane

3.1: triethylamine / methanol; dichloromethane / 0.25 h / 20 °C

3.2: 0.5 h / 20 °C

4.1: sodium tris(acetoxy)borohydride / methanol; dichloromethane

With hydrogenchloride; sodium tris(acetoxy)borohydride; triethylamine; In 1,4-dioxane; methanol; dichloromethane;
DOI:10.1128/AAC.03913-14