6-(2-fluoroethoxy)-7-methoxy-1-(4-methoxy-3-methylbenzyl)-isoquinoline oxalate

Base Information

Chemical Name:6-(2-fluoroethoxy)-7-methoxy-1-(4-methoxy-3-methylbenzyl)-isoquinoline oxalate
CAS No.:1335093-56-5
Molecular Formula:C₂H₂O₄*C₂₁H₂₂FNO₃
Molecular Weight:445.444
Hs Code.:

Synonyms:6-(2-fluoroethoxy)-7-methoxy-1-(4-methoxy-3-methylbenzyl)-isoquinoline oxalate

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Chemical Property of 6-(2-fluoroethoxy)-7-methoxy-1-(4-methoxy-3-methylbenzyl)-isoquinoline oxalate

Chemical Property:

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Technology Process of 6-(2-fluoroethoxy)-7-methoxy-1-(4-methoxy-3-methylbenzyl)-isoquinoline oxalate

There total 7 articles about 6-(2-fluoroethoxy)-7-methoxy-1-(4-methoxy-3-methylbenzyl)-isoquinoline oxalate 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:

: 1335093-38-3
6-(2-fluoroethoxy)-7-methoxy-1-(4-methoxy-3-methylbenzyl)-isoquinoline

: 144-62-7,97993-78-7
oxalic acid

: 1335093-56-5
6-(2-fluoroethoxy)-7-methoxy-1-(4-methoxy-3-methylbenzyl)-isoquinoline oxalate

Guidance literature:: In methanol; ethyl acetate; at 20 ℃; for 1h; Inert atmosphere;
DOI:10.1016/j.ejmech.2011.05.072

Reference yield:

: 621-59-0
isovanillin

: 1335093-56-5
6-(2-fluoroethoxy)-7-methoxy-1-(4-methoxy-3-methylbenzyl)-isoquinoline oxalate

Guidance literature:: Multi-step reaction with 7 steps

1.1: potassium carbonate / acetone / Reflux; Inert atmosphere

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

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

3.2: Inert atmosphere

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

5.1: 1,1'-carbonyldiimidazole / dichloromethane / 2 h / 20 °C / Inert atmosphere

5.2: Inert atmosphere

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

7.1: methanol; ethyl acetate / 1 h / 20 °C / Inert atmosphere

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

Reference yield:

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

: 1335093-56-5
6-(2-fluoroethoxy)-7-methoxy-1-(4-methoxy-3-methylbenzyl)-isoquinoline oxalate

Guidance literature:: Multi-step reaction with 6 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: methanol; ethyl acetate / 1 h / 20 °C / Inert atmosphere

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