N-[3-(2-bromo-4,5-dimethoxyphenyl)propyl]-N-(4-methoxybenzyl)-5-methyl-1-phenylhex-1-yn-3-amine

Base Information

Chemical Name:N-[3-(2-bromo-4,5-dimethoxyphenyl)propyl]-N-(4-methoxybenzyl)-5-methyl-1-phenylhex-1-yn-3-amine
CAS No.:1246965-44-5
Molecular Formula:C₃₂H₃₈BrNO₃
Molecular Weight:564.563
Hs Code.:

Synonyms:N-[3-(2-bromo-4,5-dimethoxyphenyl)propyl]-N-(4-methoxybenzyl)-5-methyl-1-phenylhex-1-yn-3-amine

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Chemical Property of N-[3-(2-bromo-4,5-dimethoxyphenyl)propyl]-N-(4-methoxybenzyl)-5-methyl-1-phenylhex-1-yn-3-amine

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Technology Process of N-[3-(2-bromo-4,5-dimethoxyphenyl)propyl]-N-(4-methoxybenzyl)-5-methyl-1-phenylhex-1-yn-3-amine

There total 1 articles about N-[3-(2-bromo-4,5-dimethoxyphenyl)propyl]-N-(4-methoxybenzyl)-5-methyl-1-phenylhex-1-yn-3-amine 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: 82.0%

: 947530-55-4
3-(2-bromo-4,5-dimethoxyphenyl)-N-(4-methoxybenzyl)propan-1-amine

: 536-74-3
phenylacetylene

: 590-86-3
isovaleraldehyde

: 1246965-44-5
N-[3-(2-bromo-4,5-dimethoxyphenyl)propyl]-N-(4-methoxybenzyl)-5-methyl-1-phenylhex-1-yn-3-amine

Guidance literature:: With copper(l) iodide; at 90 ℃; for 0.5h; Inert atmosphere; Microwave irradiation;
DOI:10.1002/ejoc.201000583

Reference yield: 40.0%

: 1246965-44-5
N-[3-(2-bromo-4,5-dimethoxyphenyl)propyl]-N-(4-methoxybenzyl)-5-methyl-1-phenylhex-1-yn-3-amine

: C₃₂H₃₉NO₃

: 1246965-64-9
(Z)-1-benzylidene-2-isobutyl-8,9-dimethoxy-3-(4-methoxybenzyl)-1,2,3,4,5,6-hexahydrobenzo[d]azocine

Guidance literature:: With tetrakis(triphenylphosphine) palladium⁽⁰⁾; sodium formate; In water; N,N-dimethyl-formamide; at 110 ℃; for 0.25h; stereoselective reaction; Inert atmosphere; Microwave irradiation;
DOI:10.1002/ejoc.201000583