(E)-N-(2-(2-methyl-3-(piperidin-1-ylmethyl)-1H-indol-1-yl)ethyl)-3-(3,4,5-trimethoxyphenyl)acrylamide

Base Information

Chemical Name:(E)-N-(2-(2-methyl-3-(piperidin-1-ylmethyl)-1H-indol-1-yl)ethyl)-3-(3,4,5-trimethoxyphenyl)acrylamide
CAS No.:1609030-74-1
Molecular Formula:C₂₉H₃₇N₃O₄
Molecular Weight:491.63
Hs Code.:

Synonyms:(E)-N-(2-(2-methyl-3-(piperidin-1-ylmethyl)-1H-indol-1-yl)ethyl)-3-(3,4,5-trimethoxyphenyl)acrylamide

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Chemical Property of (E)-N-(2-(2-methyl-3-(piperidin-1-ylmethyl)-1H-indol-1-yl)ethyl)-3-(3,4,5-trimethoxyphenyl)acrylamide

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Technology Process of (E)-N-(2-(2-methyl-3-(piperidin-1-ylmethyl)-1H-indol-1-yl)ethyl)-3-(3,4,5-trimethoxyphenyl)acrylamide

There total 5 articles about (E)-N-(2-(2-methyl-3-(piperidin-1-ylmethyl)-1H-indol-1-yl)ethyl)-3-(3,4,5-trimethoxyphenyl)acrylamide 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:

: 20329-98-0,20329-99-1,90-50-6
(E)-3,4,5-trimethoxy-cinnamic acid

: 1609031-19-7
2-(2-methyl-3-(piperidin-1-ylmethyl)-1H-indol-1-yl)ethanamine

: 1609030-74-1
(E)-N-(2-(2-methyl-3-(piperidin-1-ylmethyl)-1H-indol-1-yl)ethyl)-3-(3,4,5-trimethoxyphenyl)acrylamide

Guidance literature:: With dmap; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In dichloromethane; at 20 ℃; for 8h;
DOI:10.1021/jm5000672

Reference yield:

: 5416-80-8
2-methyl-1H-indole-3-carbaldehyde

: 1609030-74-1
(E)-N-(2-(2-methyl-3-(piperidin-1-ylmethyl)-1H-indol-1-yl)ethyl)-3-(3,4,5-trimethoxyphenyl)acrylamide

Guidance literature:: Multi-step reaction with 4 steps

1.1: sodium hydride / N,N-dimethyl-formamide / 0.5 h / 0 °C

1.2: 0 - 20 °C

2.1: acetic acid; sodium tris(acetoxy)borohydride / dichloromethane

3.1: lithium aluminium tetrahydride / tetrahydrofuran / 0 - 20 °C

4.1: 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; dmap / dichloromethane / 8 h / 20 °C

With dmap; lithium aluminium tetrahydride; sodium tris(acetoxy)borohydride; sodium hydride; acetic acid; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In tetrahydrofuran; dichloromethane; N,N-dimethyl-formamide;
DOI:10.1021/jm5000672

Reference yield:

: 1279724-51-4
2-(3-formyl-2-methyl-1H-indol-1-yl)acetonitrile

: 1609030-74-1
(E)-N-(2-(2-methyl-3-(piperidin-1-ylmethyl)-1H-indol-1-yl)ethyl)-3-(3,4,5-trimethoxyphenyl)acrylamide

Guidance literature:: Multi-step reaction with 3 steps

1: acetic acid; sodium tris(acetoxy)borohydride / dichloromethane

2: lithium aluminium tetrahydride / tetrahydrofuran / 0 - 20 °C

3: 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; dmap / dichloromethane / 8 h / 20 °C

With dmap; lithium aluminium tetrahydride; sodium tris(acetoxy)borohydride; acetic acid; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In tetrahydrofuran; dichloromethane;
DOI:10.1021/jm5000672