2-(4-{[6-nitro-1,3-dioxo-1H-benzo[de]isoquinolin-2(3H)-yl]methyl}piperidin-1-yl)ethyl 4-amino-5-chloro-2-methoxybenzoate

Base Information

Chemical Name:2-(4-{[6-nitro-1,3-dioxo-1H-benzo[de]isoquinolin-2(3H)-yl]methyl}piperidin-1-yl)ethyl 4-amino-5-chloro-2-methoxybenzoate
CAS No.:566906-40-9
Molecular Formula:C₂₈H₂₇ClN₄O₇
Molecular Weight:566.998
Hs Code.:

Synonyms:2-(4-{[6-nitro-1,3-dioxo-1H-benzo[de]isoquinolin-2(3H)-yl]methyl}piperidin-1-yl)ethyl 4-amino-5-chloro-2-methoxybenzoate

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Chemical Property of 2-(4-{[6-nitro-1,3-dioxo-1H-benzo[de]isoquinolin-2(3H)-yl]methyl}piperidin-1-yl)ethyl 4-amino-5-chloro-2-methoxybenzoate

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Technology Process of 2-(4-{[6-nitro-1,3-dioxo-1H-benzo[de]isoquinolin-2(3H)-yl]methyl}piperidin-1-yl)ethyl 4-amino-5-chloro-2-methoxybenzoate

There total 4 articles about 2-(4-{[6-nitro-1,3-dioxo-1H-benzo[de]isoquinolin-2(3H)-yl]methyl}piperidin-1-yl)ethyl 4-amino-5-chloro-2-methoxybenzoate 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: 13.0%

: 172679-60-6
4-amino-5-chloro-2-methoxybenzoic acid 2-bromoethyl ester

: 6-nitro-2-(4-piperidinemethyl)-1H-benzo[de]isoquinoline-1,3(2H)-dione hydrochloride

: 566906-40-9
2-(4-{[6-nitro-1,3-dioxo-1H-benzo[de]isoquinolin-2(3H)-yl]methyl}piperidin-1-yl)ethyl 4-amino-5-chloro-2-methoxybenzoate

Guidance literature:: With N-ethyl-N,N-diisopropylamine; In acetonitrile; for 24h; Heating;
DOI:10.1021/jm0307887

Reference yield:

: 6642-29-1
4-nitronaphthalic-1,8-anhydride

: 566906-40-9
2-(4-{[6-nitro-1,3-dioxo-1H-benzo[de]isoquinolin-2(3H)-yl]methyl}piperidin-1-yl)ethyl 4-amino-5-chloro-2-methoxybenzoate

Guidance literature:: Multi-step reaction with 3 steps

1: 71 percent / ethanol / 24 h / Heating

2: 94 percent / HCl / dioxane / 6 h / 20 °C

3: 13 percent / diisopropylethylamine / acetonitrile / 24 h / Heating

With hydrogenchloride; N-ethyl-N,N-diisopropylamine; In 1,4-dioxane; ethanol; acetonitrile;
DOI:10.1021/jm0307887

Reference yield:

: 144222-22-0
tert-butyl 4-(aminomethyl)piperidine-1-carboxylate

: 566906-40-9
2-(4-{[6-nitro-1,3-dioxo-1H-benzo[de]isoquinolin-2(3H)-yl]methyl}piperidin-1-yl)ethyl 4-amino-5-chloro-2-methoxybenzoate

Guidance literature:: Multi-step reaction with 3 steps

1: 71 percent / ethanol / 24 h / Heating

2: 94 percent / HCl / dioxane / 6 h / 20 °C

3: 13 percent / diisopropylethylamine / acetonitrile / 24 h / Heating

With hydrogenchloride; N-ethyl-N,N-diisopropylamine; In 1,4-dioxane; ethanol; acetonitrile;
DOI:10.1021/jm0307887