(E)-1-(4-(3-(5-amino-1-(chloromethyl)-1H-benzo[e]indol-3(2H)-yl)-3-oxoprop-1-enyl)phenyl)-N,N,N-trimethylmethanaminium chloride hydrochloride

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Chemical Name:(E)-1-(4-(3-(5-amino-1-(chloromethyl)-1H-benzo[e]indol-3(2H)-yl)-3-oxoprop-1-enyl)phenyl)-N,N,N-trimethylmethanaminium chloride hydrochloride
CAS No.:1017278-91-9
Molecular Formula:C₂₆H₂₉ClN₃O*ClH*Cl
Molecular Weight:506.903
Hs Code.:

Synonyms:(E)-1-(4-(3-(5-amino-1-(chloromethyl)-1H-benzo[e]indol-3(2H)-yl)-3-oxoprop-1-enyl)phenyl)-N,N,N-trimethylmethanaminium chloride hydrochloride

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Chemical Property of (E)-1-(4-(3-(5-amino-1-(chloromethyl)-1H-benzo[e]indol-3(2H)-yl)-3-oxoprop-1-enyl)phenyl)-N,N,N-trimethylmethanaminium chloride hydrochloride

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Technology Process of (E)-1-(4-(3-(5-amino-1-(chloromethyl)-1H-benzo[e]indol-3(2H)-yl)-3-oxoprop-1-enyl)phenyl)-N,N,N-trimethylmethanaminium chloride hydrochloride

There total 2 articles about (E)-1-(4-(3-(5-amino-1-(chloromethyl)-1H-benzo[e]indol-3(2H)-yl)-3-oxoprop-1-enyl)phenyl)-N,N,N-trimethylmethanaminium chloride hydrochloride 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: 79.0%

: 1017278-90-8
N-4-((E)-3-{5-[bis(tert-butoxycarbonyl)]amino-1-(chloromethyl)-1,2-dihydro-3H-benzo[e]indol-3-yl}-3-oxo-1-propenyl)benzyl-N,N,N-trimethylammonium iodide

: 1017278-91-9
(E)-1-(4-(3-(5-amino-1-(chloromethyl)-1H-benzo[e]indol-3(2H)-yl)-3-oxoprop-1-enyl)phenyl)-N,N,N-trimethylmethanaminium chloride hydrochloride

Guidance literature:: N-4-((E)-3-{5-[bis(tert-butoxycarbonyl)]amino-1-(chloromethyl)-1,2-dihydro-3H-benzo[e]indol-3-yl}-3-oxo-1-propenyl)benzyl-N,N,N-trimethylammonium iodide; With hydrogenchloride; In 1,4-dioxane; at 20 ℃; for 16h;

In methanol;
DOI:10.1016/j.bmc.2011.12.007