(S)-3-(benzyloxy)-6-((6-(benzyloxy)-7-methoxy-1,2,3,4-tetrahydroisoquinolin-1-yl)methyl)-2-methoxybenzyl acetate

Base Information

Chemical Name:(S)-3-(benzyloxy)-6-((6-(benzyloxy)-7-methoxy-1,2,3,4-tetrahydroisoquinolin-1-yl)methyl)-2-methoxybenzyl acetate
CAS No.:1422431-50-2
Molecular Formula:C₃₅H₃₇NO₆
Molecular Weight:567.682
Hs Code.:

Synonyms:(S)-3-(benzyloxy)-6-((6-(benzyloxy)-7-methoxy-1,2,3,4-tetrahydroisoquinolin-1-yl)methyl)-2-methoxybenzyl acetate

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Chemical Property of (S)-3-(benzyloxy)-6-((6-(benzyloxy)-7-methoxy-1,2,3,4-tetrahydroisoquinolin-1-yl)methyl)-2-methoxybenzyl acetate

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Technology Process of (S)-3-(benzyloxy)-6-((6-(benzyloxy)-7-methoxy-1,2,3,4-tetrahydroisoquinolin-1-yl)methyl)-2-methoxybenzyl acetate

There total 12 articles about (S)-3-(benzyloxy)-6-((6-(benzyloxy)-7-methoxy-1,2,3,4-tetrahydroisoquinolin-1-yl)methyl)-2-methoxybenzyl acetate 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:

: 1422431-42-2
3-(benzyloxy)-6-((6-(benzyloxy)-7-methoxy-3,4-dihydroisoquinolin-1-yl)methyl)-2-methoxybenzyl acetate

: 1422431-50-2
(S)-3-(benzyloxy)-6-((6-(benzyloxy)-7-methoxy-1,2,3,4-tetrahydroisoquinolin-1-yl)methyl)-2-methoxybenzyl acetate

Guidance literature:: With (1S,2S)-(+)-N-tosyl-1,2-diphenylethane-1,2-diamine[η6-1-isopropyl-4-methylbenzene]-ruthenium(II); formic acid; triethylamine; In N,N-dimethyl-formamide; at 20 ℃;
DOI:10.1016/j.bmc.2012.12.016

Reference yield:

: 1422431-35-3
3-(benzyloxy)-6-(2-(3-(benzyloxy)-4-methoxyphenethylamino)-2-oxoethyl)-2-methoxybenzyl acetate

: 1422431-50-2
(S)-3-(benzyloxy)-6-((6-(benzyloxy)-7-methoxy-1,2,3,4-tetrahydroisoquinolin-1-yl)methyl)-2-methoxybenzyl acetate

Guidance literature:: Multi-step reaction with 2 steps

1: trichlorophosphate / acetonitrile / 1 h / Reflux; Inert atmosphere

2: (1S,2S)-(+)-N-tosyl-1,2-diphenylethane-1,2-diamine[η6-1-isopropyl-4-methylbenzene]-ruthenium(II); formic acid; triethylamine / N,N-dimethyl-formamide / 20 °C

With (1S,2S)-(+)-N-tosyl-1,2-diphenylethane-1,2-diamine[η6-1-isopropyl-4-methylbenzene]-ruthenium(II); formic acid; triethylamine; trichlorophosphate; In N,N-dimethyl-formamide; acetonitrile; 1: |Bischler-Napieralski Reaction;
DOI:10.1016/j.bmc.2012.12.016

Reference yield:

: 63909-29-5,55507-05-6
3-benzyloxy-4-methoxy-β-nitrostyrene

: 1422431-50-2
(S)-3-(benzyloxy)-6-((6-(benzyloxy)-7-methoxy-1,2,3,4-tetrahydroisoquinolin-1-yl)methyl)-2-methoxybenzyl acetate

Guidance literature:: Multi-step reaction with 5 steps

1: lithium aluminium tetrahydride / tetrahydrofuran / 2 h / Reflux

2: ethanol / 14 h / Reflux

3: pyridine / dichloromethane / 1.5 h / 0 - 20 °C

4: trichlorophosphate / acetonitrile / 1 h / Reflux; Inert atmosphere

5: (1S,2S)-(+)-N-tosyl-1,2-diphenylethane-1,2-diamine[η6-1-isopropyl-4-methylbenzene]-ruthenium(II); formic acid; triethylamine / N,N-dimethyl-formamide / 20 °C

With pyridine; lithium aluminium tetrahydride; (1S,2S)-(+)-N-tosyl-1,2-diphenylethane-1,2-diamine[η6-1-isopropyl-4-methylbenzene]-ruthenium(II); formic acid; triethylamine; trichlorophosphate; In tetrahydrofuran; ethanol; dichloromethane; N,N-dimethyl-formamide; acetonitrile; 4: |Bischler-Napieralski Reaction;
DOI:10.1016/j.bmc.2012.12.016