4-(3,5-dimethoxy-4-propoxybenzyl)-7-ethoxyisoquinolin-8-yl trifluoromethanesulfonate

Base Information

Chemical Name:4-(3,5-dimethoxy-4-propoxybenzyl)-7-ethoxyisoquinolin-8-yl trifluoromethanesulfonate
CAS No.:1351593-44-6
Molecular Formula:C₂₄H₂₆F₃NO₇S
Molecular Weight:529.534
Hs Code.:

Synonyms:4-(3,5-dimethoxy-4-propoxybenzyl)-7-ethoxyisoquinolin-8-yl trifluoromethanesulfonate

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Chemical Property of 4-(3,5-dimethoxy-4-propoxybenzyl)-7-ethoxyisoquinolin-8-yl trifluoromethanesulfonate

Chemical Property:

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Technology Process of 4-(3,5-dimethoxy-4-propoxybenzyl)-7-ethoxyisoquinolin-8-yl trifluoromethanesulfonate

There total 6 articles about 4-(3,5-dimethoxy-4-propoxybenzyl)-7-ethoxyisoquinolin-8-yl trifluoromethanesulfonate 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: 60.0%

: 37595-74-7
N,N-phenylbistrifluoromethane-sulfonimide

: 1351592-44-3
4-(3,5-dimethoxy-4-propoxybenzyl)-7-ethoxyisoquinolin-8-ol

: 1351593-44-6
4-(3,5-dimethoxy-4-propoxybenzyl)-7-ethoxyisoquinolin-8-yl trifluoromethanesulfonate

Guidance literature:: With triethylamine; In dichloromethane; at 20 ℃;

Reference yield:

: 492-88-6
3-ethoxysalicylaldehyde

: 1351593-44-6
4-(3,5-dimethoxy-4-propoxybenzyl)-7-ethoxyisoquinolin-8-yl trifluoromethanesulfonate

Guidance literature:: Multi-step reaction with 4 steps

1: toluene / 4 h / 150 °C / Inert atmosphere

2: ethanol; sodium tetrahydroborate / 1 h / 100 °C / Inert atmosphere

3: hydrogenchloride / ethanol; water / 0.42 h / 90 °C

4: triethylamine / dichloromethane / 20 °C

With hydrogenchloride; sodium tetrahydroborate; ethanol; triethylamine; In ethanol; dichloromethane; water; toluene;

Reference yield:

: 134-96-3
syringic aldehyde

: 1351593-44-6
4-(3,5-dimethoxy-4-propoxybenzyl)-7-ethoxyisoquinolin-8-yl trifluoromethanesulfonate

Guidance literature:: Multi-step reaction with 3 steps

1: caesium carbonate / N,N-dimethyl-formamide / 10 h / 40 °C / Inert atmosphere

2: hydrogenchloride / ethanol; water / 0.42 h / 90 °C

3: triethylamine / dichloromethane / 20 °C

With hydrogenchloride; caesium carbonate; triethylamine; In ethanol; dichloromethane; water; N,N-dimethyl-formamide;