7-(2-fluoroethoxy)-1-(4-(2-fluoroethoxy)-3-methoxybenzyl)-6-methoxyisoquinoline

Base Information

Chemical Name:7-(2-fluoroethoxy)-1-(4-(2-fluoroethoxy)-3-methoxybenzyl)-6-methoxyisoquinoline
CAS No.:1335093-52-1
Molecular Formula:C₂₂H₂₃F₂NO₄
Molecular Weight:403.426
Hs Code.:

Synonyms:7-(2-fluoroethoxy)-1-(4-(2-fluoroethoxy)-3-methoxybenzyl)-6-methoxyisoquinoline

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Chemical Property of 7-(2-fluoroethoxy)-1-(4-(2-fluoroethoxy)-3-methoxybenzyl)-6-methoxyisoquinoline

Chemical Property:

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Technology Process of 7-(2-fluoroethoxy)-1-(4-(2-fluoroethoxy)-3-methoxybenzyl)-6-methoxyisoquinoline

There total 7 articles about 7-(2-fluoroethoxy)-1-(4-(2-fluoroethoxy)-3-methoxybenzyl)-6-methoxyisoquinoline 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:

: 914394-64-2
4-(2-fluoroethoxy)-3-methoxybenzaldehyde

: 1335093-52-1
7-(2-fluoroethoxy)-1-(4-(2-fluoroethoxy)-3-methoxybenzyl)-6-methoxyisoquinoline

Guidance literature:: Multi-step reaction with 7 steps

1.1: ammonium acetate; acetic acid / 0.5 h / Reflux; Inert atmosphere

2.1: tetrahydrofuran; methanol / 20 °C / Inert atmosphere

2.2: Inert atmosphere

3.1: lithium aluminium tetrahydride / tetrahydrofuran / Reflux; Inert atmosphere

4.1: 1,1'-carbonyldiimidazole / dichloromethane / 2 h / 20 °C / Inert atmosphere

4.2: Inert atmosphere

5.1: trichlorophosphate / acetonitrile / 0.5 h / Reflux; Inert atmosphere

6.1: hydrogenchloride / ethanol; water / 2 h / Reflux; Inert atmosphere

7.1: potassium carbonate / acetone / Reflux; Inert atmosphere

With hydrogenchloride; lithium aluminium tetrahydride; ammonium acetate; potassium carbonate; acetic acid; 1,1'-carbonyldiimidazole; trichlorophosphate; In tetrahydrofuran; methanol; ethanol; dichloromethane; water; acetone; acetonitrile;
DOI:10.1016/j.ejmech.2011.05.072

Reference yield:

: 1335093-86-1
2-(4-(benzyloxy)-3-methoxyphenyl)-N-(2-(4-(2-fluoroethoxy)-3-methoxyphenyl)-2-methoxyethyl)acetamide

: 1335093-52-1
7-(2-fluoroethoxy)-1-(4-(2-fluoroethoxy)-3-methoxybenzyl)-6-methoxyisoquinoline

Guidance literature:: Multi-step reaction with 3 steps

1: trichlorophosphate / acetonitrile / 0.5 h / Reflux; Inert atmosphere

2: hydrogenchloride / ethanol; water / 2 h / Reflux; Inert atmosphere

3: potassium carbonate / acetone / Reflux; Inert atmosphere

With hydrogenchloride; potassium carbonate; trichlorophosphate; In ethanol; water; acetone; acetonitrile;
DOI:10.1016/j.ejmech.2011.05.072

Reference yield:

: 1335093-51-0
1-(4-(benzyloxy)-3-methoxybenzyl)-7-(2-fluoroethoxy)-6-methoxyisoquinoline

: 1335093-52-1
7-(2-fluoroethoxy)-1-(4-(2-fluoroethoxy)-3-methoxybenzyl)-6-methoxyisoquinoline

Guidance literature:: Multi-step reaction with 2 steps

1: hydrogenchloride / ethanol; water / 2 h / Reflux; Inert atmosphere

2: potassium carbonate / acetone / Reflux; Inert atmosphere

With hydrogenchloride; potassium carbonate; In ethanol; water; acetone;
DOI:10.1016/j.ejmech.2011.05.072