(E)-2-sec-butyl-6-((2-(7-chloroquinolin-4-ylamino)ethylamino)methylene)-4-((E)-3-oxo-3-(thiophen-2-yl)prop-1-enyl)cyclohexa-2,4-dienone

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Chemical Name:(E)-2-sec-butyl-6-((2-(7-chloroquinolin-4-ylamino)ethylamino)methylene)-4-((E)-3-oxo-3-(thiophen-2-yl)prop-1-enyl)cyclohexa-2,4-dienone
CAS No.:1375171-29-1
Molecular Formula:C₂₉H₂₈ClN₃O₂S
Molecular Weight:518.079
Hs Code.:

Synonyms:(E)-2-sec-butyl-6-((2-(7-chloroquinolin-4-ylamino)ethylamino)methylene)-4-((E)-3-oxo-3-(thiophen-2-yl)prop-1-enyl)cyclohexa-2,4-dienone

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Chemical Property of (E)-2-sec-butyl-6-((2-(7-chloroquinolin-4-ylamino)ethylamino)methylene)-4-((E)-3-oxo-3-(thiophen-2-yl)prop-1-enyl)cyclohexa-2,4-dienone

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Technology Process of (E)-2-sec-butyl-6-((2-(7-chloroquinolin-4-ylamino)ethylamino)methylene)-4-((E)-3-oxo-3-(thiophen-2-yl)prop-1-enyl)cyclohexa-2,4-dienone

There total 4 articles about (E)-2-sec-butyl-6-((2-(7-chloroquinolin-4-ylamino)ethylamino)methylene)-4-((E)-3-oxo-3-(thiophen-2-yl)prop-1-enyl)cyclohexa-2,4-dienone 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: 91.0%

: 5407-57-8
N-(7-chloroquinolin-4-yl)ethylenediamine

: 1375171-68-8
C₁₈H₁₈O₃S

: 1375171-29-1
(E)-2-sec-butyl-6-((2-(7-chloroquinolin-4-ylamino)ethylamino)methylene)-4-((E)-3-oxo-3-(thiophen-2-yl)prop-1-enyl)cyclohexa-2,4-dienone

Guidance literature:: In ethanol; at 20 ℃; for 0.166667h;
DOI:10.1016/j.bmc.2012.03.011

Reference yield:

: 89-72-5
2-sec-butylphenol

: 1375171-29-1
(E)-2-sec-butyl-6-((2-(7-chloroquinolin-4-ylamino)ethylamino)methylene)-4-((E)-3-oxo-3-(thiophen-2-yl)prop-1-enyl)cyclohexa-2,4-dienone

Guidance literature:: Multi-step reaction with 3 steps

1.1: trifluoroacetic acid / 3 h / 120 °C

1.2: 2 h / 90 - 100 °C

2.1: hydrogenchloride / 1,4-dioxane; water / 80 - 90 °C

3.1: ethanol / 0.17 h / 20 °C

With hydrogenchloride; trifluoroacetic acid; In 1,4-dioxane; ethanol; water; 1.1: Duff reaction;
DOI:10.1016/j.bmc.2012.03.011

Reference yield:

: 88-15-3,97511-16-5
2-Acetylthiophene

: 1257865-15-8
5-(sec-butyl)-4-hydroxybenzene-1,3-dicarbaldehyde

: 1375171-29-1
(E)-2-sec-butyl-6-((2-(7-chloroquinolin-4-ylamino)ethylamino)methylene)-4-((E)-3-oxo-3-(thiophen-2-yl)prop-1-enyl)cyclohexa-2,4-dienone

Guidance literature:: Multi-step reaction with 2 steps

1: hydrogenchloride / 1,4-dioxane; water / 80 - 90 °C

2: ethanol / 0.17 h / 20 °C

With hydrogenchloride; In 1,4-dioxane; ethanol; water;
DOI:10.1016/j.bmc.2012.03.011