6,7-dimethoxy-1-(4-((6-(piperidin-1-yl)hexyl)oxy)benzyl)-1,2,3,4-tetrahydroisoquinoline

Base Information

Chemical Name:6,7-dimethoxy-1-(4-((6-(piperidin-1-yl)hexyl)oxy)benzyl)-1,2,3,4-tetrahydroisoquinoline
CAS No.:1609169-46-1
Molecular Formula:C₂₉H₄₂N₂O₃
Molecular Weight:466.664
Hs Code.:

Synonyms:6,7-dimethoxy-1-(4-((6-(piperidin-1-yl)hexyl)oxy)benzyl)-1,2,3,4-tetrahydroisoquinoline

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Chemical Property of 6,7-dimethoxy-1-(4-((6-(piperidin-1-yl)hexyl)oxy)benzyl)-1,2,3,4-tetrahydroisoquinoline

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Technology Process of 6,7-dimethoxy-1-(4-((6-(piperidin-1-yl)hexyl)oxy)benzyl)-1,2,3,4-tetrahydroisoquinoline

There total 10 articles about 6,7-dimethoxy-1-(4-((6-(piperidin-1-yl)hexyl)oxy)benzyl)-1,2,3,4-tetrahydroisoquinoline 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: 84.5%

: 1609169-78-9
tert-butyl 6,7-dimethoxy-1-(4-((6-(piperidin-1-yl)hexyl)oxy)benzyl)-3,4-dihydroisoquinoline-2(1H)-carboxylate

: 1609169-46-1
6,7-dimethoxy-1-(4-((6-(piperidin-1-yl)hexyl)oxy)benzyl)-1,2,3,4-tetrahydroisoquinoline

Guidance literature:: With hydrogenchloride; In diethyl ether; at 20 ℃; for 3h;
DOI:10.1016/j.bmcl.2014.03.058

Reference yield:

: 1609169-64-3
tert-butyl 1-(4-((6-bromohexyl)oxy)benzyl)-6,7-dimethoxy-3,4-dihydroisoquinoline-2(1H)-carboxylate

: 1609169-46-1
6,7-dimethoxy-1-(4-((6-(piperidin-1-yl)hexyl)oxy)benzyl)-1,2,3,4-tetrahydroisoquinoline

Guidance literature:: Multi-step reaction with 2 steps

1: sodium hydrogencarbonate / N,N-dimethyl-formamide / 24 h / 60 °C

2: hydrogenchloride / diethyl ether / 3 h / 20 °C

With hydrogenchloride; sodium hydrogencarbonate; In diethyl ether; N,N-dimethyl-formamide;
DOI:10.1016/j.bmcl.2014.03.058

Reference yield:

: 10214-84-3
N-[2-(3,4-dimethoxyphenyl)ethyl]-2-(4-hydroxyphenyl)acetamide

: 1609169-46-1
6,7-dimethoxy-1-(4-((6-(piperidin-1-yl)hexyl)oxy)benzyl)-1,2,3,4-tetrahydroisoquinoline

Guidance literature:: Multi-step reaction with 8 steps

1: potassium carbonate / ethanol / 12 h / Reflux

2: trichlorophosphate / toluene / 4 h / 20 °C / Reflux

3: sodium tetrahydroborate / methanol / 6 h / 0 - 20 °C

4: dichloromethane / 2 h / 20 °C

5: palladium 10% on activated carbon; hydrogen / methanol / 48 h

6: potassium carbonate / butanone / 6 h / Reflux

7: sodium hydrogencarbonate / N,N-dimethyl-formamide / 24 h / 60 °C

8: hydrogenchloride / diethyl ether / 3 h / 20 °C

With hydrogenchloride; sodium tetrahydroborate; palladium 10% on activated carbon; hydrogen; sodium hydrogencarbonate; potassium carbonate; trichlorophosphate; In methanol; diethyl ether; ethanol; dichloromethane; N,N-dimethyl-formamide; toluene; butanone; 2: |Bischler-Napieralski Reaction;
DOI:10.1016/j.bmcl.2014.03.058