(E)-N',N'-diethyl-3-[N-(2-iodo-4,5-dimethoxybenzyl)-1H-pyrrol-2-yl]acrylamide

Base Information

Chemical Name:(E)-N',N'-diethyl-3-[N-(2-iodo-4,5-dimethoxybenzyl)-1H-pyrrol-2-yl]acrylamide
CAS No.:1213766-87-0
Molecular Formula:C₂₀H₂₅IN₂O₃
Molecular Weight:468.335
Hs Code.:

Synonyms:(E)-N',N'-diethyl-3-[N-(2-iodo-4,5-dimethoxybenzyl)-1H-pyrrol-2-yl]acrylamide

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Chemical Property of (E)-N',N'-diethyl-3-[N-(2-iodo-4,5-dimethoxybenzyl)-1H-pyrrol-2-yl]acrylamide

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Technology Process of (E)-N',N'-diethyl-3-[N-(2-iodo-4,5-dimethoxybenzyl)-1H-pyrrol-2-yl]acrylamide

There total 3 articles about (E)-N',N'-diethyl-3-[N-(2-iodo-4,5-dimethoxybenzyl)-1H-pyrrol-2-yl]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: 97.0%

: 1133436-77-7
1-(2-iodo-4,5-dimethoxybenzyl)-1H-pyrrole-2-carbaldehyde

: 6080-83-7
<(N,N-Diethylcarbamoyl)methylidene>triphenylphosphorane

: 1213766-87-0
(E)-N',N'-diethyl-3-[N-(2-iodo-4,5-dimethoxybenzyl)-1H-pyrrol-2-yl]acrylamide

Guidance literature:: In dichloromethane; for 96h; Reflux; Inert atmosphere;
DOI:10.1002/adsc.200900368

Reference yield:

: 293732-19-1
(4,5-dimethoxy-2-iodophenyl)methyl bromide

: 1213766-87-0
(E)-N',N'-diethyl-3-[N-(2-iodo-4,5-dimethoxybenzyl)-1H-pyrrol-2-yl]acrylamide

Guidance literature:: Multi-step reaction with 2 steps

1.1: potassium hydroxide / dimethyl sulfoxide / 2 h / 20 °C

1.2: 4 h

2.1: dichloromethane / 96 h / Reflux

With potassium hydroxide; In dichloromethane; dimethyl sulfoxide; 2.1: |Wittig Olefination;
DOI:10.1002/ejoc.201200994

Reference yield:

: 1003-29-8,254729-95-8
2-pyrrole aldehyde

: 1213766-87-0
(E)-N',N'-diethyl-3-[N-(2-iodo-4,5-dimethoxybenzyl)-1H-pyrrol-2-yl]acrylamide

Guidance literature:: Multi-step reaction with 2 steps

1.1: potassium hydroxide / dimethyl sulfoxide / 2 h / 20 °C

1.2: 4 h

2.1: dichloromethane / 96 h / Reflux

With potassium hydroxide; In dichloromethane; dimethyl sulfoxide; 2.1: |Wittig Olefination;
DOI:10.1002/ejoc.201200994