(E)-N-(3-(2-fluoro-4-methoxyphenyl)-2-methylallyl)-3,4,5-trimethoxy-N-(2-(1-methylpyrrolidin-2-yl)ethyl)benzamide

Base Information

Chemical Name:(E)-N-(3-(2-fluoro-4-methoxyphenyl)-2-methylallyl)-3,4,5-trimethoxy-N-(2-(1-methylpyrrolidin-2-yl)ethyl)benzamide
CAS No.:1375800-59-1
Molecular Formula:C₂₈H₃₇FN₂O₅
Molecular Weight:500.611
Hs Code.:

Synonyms:(E)-N-(3-(2-fluoro-4-methoxyphenyl)-2-methylallyl)-3,4,5-trimethoxy-N-(2-(1-methylpyrrolidin-2-yl)ethyl)benzamide

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Chemical Property of (E)-N-(3-(2-fluoro-4-methoxyphenyl)-2-methylallyl)-3,4,5-trimethoxy-N-(2-(1-methylpyrrolidin-2-yl)ethyl)benzamide

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Technology Process of (E)-N-(3-(2-fluoro-4-methoxyphenyl)-2-methylallyl)-3,4,5-trimethoxy-N-(2-(1-methylpyrrolidin-2-yl)ethyl)benzamide

There total 4 articles about (E)-N-(3-(2-fluoro-4-methoxyphenyl)-2-methylallyl)-3,4,5-trimethoxy-N-(2-(1-methylpyrrolidin-2-yl)ethyl)benzamide 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:

: 1375800-72-8
(E)-3-(2-fluoro-4-methoxyphenyl)-2-methyl-N-(2-(1-methylpyrrolidin-2-yl)ethyl)prop-2-en-1-amine

: 4521-61-3
3,4,5-Trimethoxybenzoyl chloride

: 1375800-59-1
(E)-N-(3-(2-fluoro-4-methoxyphenyl)-2-methylallyl)-3,4,5-trimethoxy-N-(2-(1-methylpyrrolidin-2-yl)ethyl)benzamide

Guidance literature:: With triethylamine; In dichloromethane; at 20 ℃; for 2h; Inert atmosphere;
DOI:10.1016/j.ejmech.2012.02.041

Reference yield:

: 1375800-41-1
(E)-3-(2-fluoro-4-methoxyphenyl)-2-methylacrylaldehyde

: 1375800-59-1
(E)-N-(3-(2-fluoro-4-methoxyphenyl)-2-methylallyl)-3,4,5-trimethoxy-N-(2-(1-methylpyrrolidin-2-yl)ethyl)benzamide

Guidance literature:: Multi-step reaction with 3 steps

1.1: magnesium sulfate / dichloromethane / 96 h / 20 °C / Inert atmosphere

2.1: sodium tetrahydroborate / methanol / 1 h / 0 °C / Inert atmosphere

2.2: 0.17 h / 20 °C

2.3: pH > 10

3.1: triethylamine / dichloromethane / 2 h / 20 °C / Inert atmosphere

With sodium tetrahydroborate; magnesium sulfate; triethylamine; In methanol; dichloromethane;
DOI:10.1016/j.ejmech.2012.02.041

Reference yield:

: 118-41-2
Eudesmic acid

: 1375800-59-1
(E)-N-(3-(2-fluoro-4-methoxyphenyl)-2-methylallyl)-3,4,5-trimethoxy-N-(2-(1-methylpyrrolidin-2-yl)ethyl)benzamide

Guidance literature:: Multi-step reaction with 2 steps

1: thionyl chloride / 2 h / Reflux

2: triethylamine / dichloromethane / 2 h / 20 °C / Inert atmosphere

With thionyl chloride; triethylamine; In dichloromethane;
DOI:10.1016/j.ejmech.2012.02.041