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

Base Information

Chemical Name:6,7-dimethoxy-1-(4-((6-(4-phenylpiperidin-1-yl)hexyl)oxy)benzyl)-1,2,3,4-tetrahydroisoquinoline
CAS No.:1609169-53-0
Molecular Formula:C₃₅H₄₆N₂O₃
Molecular Weight:542.762
Hs Code.:

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

Suppliers and Price of 6,7-dimethoxy-1-(4-((6-(4-phenylpiperidin-1-yl)hexyl)oxy)benzyl)-1,2,3,4-tetrahydroisoquinoline

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 0 raw suppliers

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

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

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

There total 10 articles about 6,7-dimethoxy-1-(4-((6-(4-phenylpiperidin-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: 84.3%

: 1609169-85-8
tert-butyl 6,7-dimethoxy-1-(4-((6-(4-phenylpiperidin-1-yl)hexyl)oxy)benzyl)-3,4-dihydroisoquinoline-2(1H)-carboxylate

: 1609169-53-0
6,7-dimethoxy-1-(4-((6-(4-phenylpiperidin-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

: 1609169-53-0
6,7-dimethoxy-1-(4-((6-(4-phenylpiperidin-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

: 1609169-53-0
6,7-dimethoxy-1-(4-((6-(4-phenylpiperidin-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