(E)-9-methoxy-6-(4-methoxyphenyl)-11H-indeno[1,2-c]quinolin-11-one O-2-(pyrrolidin-1-yl)ethyl oxime

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Chemical Name:(E)-9-methoxy-6-(4-methoxyphenyl)-11H-indeno[1,2-c]quinolin-11-one O-2-(pyrrolidin-1-yl)ethyl oxime
CAS No.:1352150-46-9
Molecular Formula:C₃₀H₂₉N₃O₃
Molecular Weight:479.579
Hs Code.:

Synonyms:(E)-9-methoxy-6-(4-methoxyphenyl)-11H-indeno[1,2-c]quinolin-11-one O-2-(pyrrolidin-1-yl)ethyl oxime

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Chemical Property of (E)-9-methoxy-6-(4-methoxyphenyl)-11H-indeno[1,2-c]quinolin-11-one O-2-(pyrrolidin-1-yl)ethyl oxime

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Technology Process of (E)-9-methoxy-6-(4-methoxyphenyl)-11H-indeno[1,2-c]quinolin-11-one O-2-(pyrrolidin-1-yl)ethyl oxime

There total 2 articles about (E)-9-methoxy-6-(4-methoxyphenyl)-11H-indeno[1,2-c]quinolin-11-one O-2-(pyrrolidin-1-yl)ethyl oxime 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: 86.0%

: 5050-41-9
N-(2-chloroethyl)-pyrrolidine

: (E)-9-methoxy-6-(4-methoxyphenyl)-11H-indeno[1,2-c]quinolin-11-one oxime hydrochloride

: 1352150-46-9
(E)-9-methoxy-6-(4-methoxyphenyl)-11H-indeno[1,2-c]quinolin-11-one O-2-(pyrrolidin-1-yl)ethyl oxime

Guidance literature:: (E)-9-methoxy-6-(4-methoxyphenyl)-11H-indeno[1,2-c]quinolin-11-one oxime hydrochloride; With sodium hydride; In N,N-dimethyl-formamide; mineral oil; at 0 ℃; for 1h;

N-(2-chloroethyl)-pyrrolidine; In N,N-dimethyl-formamide; mineral oil; at 80 ℃; for 1h;
DOI:10.1016/j.bmc.2011.10.014

Reference yield:

: 1198747-69-1
9-methoxy-6-(4-methoxyphenyl)-11H-indeno[1,2-c]quinolin-11-one

: 1352150-46-9
(E)-9-methoxy-6-(4-methoxyphenyl)-11H-indeno[1,2-c]quinolin-11-one O-2-(pyrrolidin-1-yl)ethyl oxime

Guidance literature:: Multi-step reaction with 2 steps

1.1: hydroxylamine hydrochloride / 2-ethoxy-ethanol / 3 h / Reflux

2.1: sodium hydride / N,N-dimethyl-formamide; mineral oil / 1 h / 0 °C

2.2: 1 h / 80 °C

With hydroxylamine hydrochloride; sodium hydride; In 2-ethoxy-ethanol; N,N-dimethyl-formamide; mineral oil;
DOI:10.1016/j.bmc.2011.10.014