6-methoxy-1-methyl-1-[4-(2-piperidin-1-yl-ethoxy)-phenyl]-2-p-tolyl-1,2,3,4-tetrahydro-isoquinoline

Base Information

Chemical Name:6-methoxy-1-methyl-1-[4-(2-piperidin-1-yl-ethoxy)-phenyl]-2-p-tolyl-1,2,3,4-tetrahydro-isoquinoline
CAS No.:645398-55-6
Molecular Formula:C₃₁H₃₈N₂O₂
Molecular Weight:470.655
Hs Code.:

6-methoxy-1-methyl-1-[4-(2-piperidin-1-yl-ethoxy)-phenyl]-2-<i>p</i>-tolyl-1,2,3,4-tetrahydro-isoquinoline

Synonyms:6-methoxy-1-methyl-1-[4-(2-piperidin-1-yl-ethoxy)-phenyl]-2-p-tolyl-1,2,3,4-tetrahydro-isoquinoline

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Chemical Property of 6-methoxy-1-methyl-1-[4-(2-piperidin-1-yl-ethoxy)-phenyl]-2-p-tolyl-1,2,3,4-tetrahydro-isoquinoline

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Technology Process of 6-methoxy-1-methyl-1-[4-(2-piperidin-1-yl-ethoxy)-phenyl]-2-p-tolyl-1,2,3,4-tetrahydro-isoquinoline

There total 7 articles about 6-methoxy-1-methyl-1-[4-(2-piperidin-1-yl-ethoxy)-phenyl]-2-p-tolyl-1,2,3,4-tetrahydro-isoquinoline 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:

: 2008-75-5
N-chloroethylpiperidine hydrochloride

: 645393-66-4
4-(6-methoxy-1-methyl-2-p-tolyl-1,2,3,4-tetrahydro-isoquinolin-1-yl)-phenol

: 645398-55-6
6-methoxy-1-methyl-1-[4-(2-piperidin-1-yl-ethoxy)-phenyl]-2-p-tolyl-1,2,3,4-tetrahydro-isoquinoline

Guidance literature:: 4-(6-methoxy-1-methyl-2-p-tolyl-1,2,3,4-tetrahydro-isoquinolin-1-yl)-phenol; With sodium hydride; In 1,4-dioxane; at 20 ℃;

N-chloroethylpiperidine hydrochloride; With sodium hydride; In 1,4-dioxane; at 80 ℃;
DOI:10.1021/jm030086h

Reference yield:

: 624-31-7
4-tolyl iodide

: 645398-55-6
6-methoxy-1-methyl-1-[4-(2-piperidin-1-yl-ethoxy)-phenyl]-2-p-tolyl-1,2,3,4-tetrahydro-isoquinoline

Guidance literature:: Multi-step reaction with 5 steps

1.1: CuI; K₂CO₃ / dimethylformamide / 150 °C

2.1: hexane; tetrahydrofuran / -78 °C

2.2: aq. HClO₄ / hexane; tetrahydrofuran; ethyl acetate / 0.17 h

3.1: tetrahydrofuran; diethyl ether / 0 - 20 °C

4.1: AlCl₃; Me₂NPh / CH₂Cl₂ / 20 °C

5.1: NaH / dioxane / 20 °C

5.2: NaH / dioxane / 80 °C

With copper(l) iodide; aluminium trichloride; sodium hydride; potassium carbonate; N,N-dimethyl-aniline; In tetrahydrofuran; 1,4-dioxane; diethyl ether; hexane; dichloromethane; N,N-dimethyl-formamide; 1.1: Ullmann reaction;
DOI:10.1021/jm030086h

Reference yield:

: 4-Benzyloxyphenyl lithium

: 645398-55-6
6-methoxy-1-methyl-1-[4-(2-piperidin-1-yl-ethoxy)-phenyl]-2-p-tolyl-1,2,3,4-tetrahydro-isoquinoline

Guidance literature:: Multi-step reaction with 4 steps

1.1: hexane; tetrahydrofuran / -78 °C

1.2: aq. HClO₄ / hexane; tetrahydrofuran; ethyl acetate / 0.17 h

2.1: tetrahydrofuran; diethyl ether / 0 - 20 °C

3.1: AlCl₃; Me₂NPh / CH₂Cl₂ / 20 °C

4.1: NaH / dioxane / 20 °C

4.2: NaH / dioxane / 80 °C

With aluminium trichloride; sodium hydride; N,N-dimethyl-aniline; In tetrahydrofuran; 1,4-dioxane; diethyl ether; hexane; dichloromethane;
DOI:10.1021/jm030086h