(S,E)-1-(3-(4-chlorophenyl)allyl)-1-(1-(3,4-dihydroquinolin-1(2H)-yl)-1-oxopropan-2-yl)piperidin-1-ium bromide

Base Information

Chemical Name:(S,E)-1-(3-(4-chlorophenyl)allyl)-1-(1-(3,4-dihydroquinolin-1(2H)-yl)-1-oxopropan-2-yl)piperidin-1-ium bromide
CAS No.:1613244-44-2
Molecular Formula:Br*C₂₆H₃₂ClN₂O
Molecular Weight:503.91
Hs Code.:

Synonyms:(S,E)-1-(3-(4-chlorophenyl)allyl)-1-(1-(3,4-dihydroquinolin-1(2H)-yl)-1-oxopropan-2-yl)piperidin-1-ium bromide

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Chemical Property of (S,E)-1-(3-(4-chlorophenyl)allyl)-1-(1-(3,4-dihydroquinolin-1(2H)-yl)-1-oxopropan-2-yl)piperidin-1-ium bromide

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Technology Process of (S,E)-1-(3-(4-chlorophenyl)allyl)-1-(1-(3,4-dihydroquinolin-1(2H)-yl)-1-oxopropan-2-yl)piperidin-1-ium bromide

There total 6 articles about (S,E)-1-(3-(4-chlorophenyl)allyl)-1-(1-(3,4-dihydroquinolin-1(2H)-yl)-1-oxopropan-2-yl)piperidin-1-ium bromide 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%

: 1613244-01-1
(S)-1-(3,4-dihydroquinolin-1(2H)-yl)-2-(piperidin-1-yl)propan-1-one

: 42432-30-4,60691-90-9
p-chlorocinnamyl bromide

: 1613244-44-2
(S,E)-1-(3-(4-chlorophenyl)allyl)-1-(1-(3,4-dihydroquinolin-1(2H)-yl)-1-oxopropan-2-yl)piperidin-1-ium bromide

Guidance literature:: In acetonitrile; at 20 ℃; for 60h;
DOI:10.1039/c4cc02536a

Reference yield:

: 24393-52-0
ethyl (E)-3-(4-chlorophenyl)prop-2-enoate

: 1613244-44-2
(S,E)-1-(3-(4-chlorophenyl)allyl)-1-(1-(3,4-dihydroquinolin-1(2H)-yl)-1-oxopropan-2-yl)piperidin-1-ium bromide

Guidance literature:: Multi-step reaction with 3 steps

1: diisobutylaluminium hydride / toluene; hexane / 0.5 h / 0 °C

2: phosphorus tribromide / diethyl ether / 2.5 h / 0 - 20 °C

3: acetonitrile / 60 h / 20 °C

With phosphorus tribromide; diisobutylaluminium hydride; In diethyl ether; hexane; toluene; acetonitrile;
DOI:10.1039/c4cc02536a

Reference yield:

: 1613243-98-3
(S)-benzyl (1-(3,4-dihydroquinolin-1(2H)-yl)-1-oxopropan-2-yl)carbamate

: 1613244-44-2
(S,E)-1-(3-(4-chlorophenyl)allyl)-1-(1-(3,4-dihydroquinolin-1(2H)-yl)-1-oxopropan-2-yl)piperidin-1-ium bromide

Guidance literature:: Multi-step reaction with 3 steps

1: palladium 10% on activated carbon; hydrogen / methanol / 5 h / 20 °C

2: sodium hydrogencarbonate / acetonitrile / 12 h / Reflux

3: acetonitrile / 60 h / 20 °C

With palladium 10% on activated carbon; hydrogen; sodium hydrogencarbonate; In methanol; acetonitrile;
DOI:10.1039/c4cc02536a