N-[3-(4-methoxybenzylidene)-2-oxoindolin-6-yl-carbamoyl]4-methoxybenzamide

Base Information

Chemical Name:N-[3-(4-methoxybenzylidene)-2-oxoindolin-6-yl-carbamoyl]4-methoxybenzamide
CAS No.:1621584-54-0
Molecular Formula:C₂₅H₂₁N₃O₅
Molecular Weight:443.459
Hs Code.:

Synonyms:N-[3-(4-methoxybenzylidene)-2-oxoindolin-6-yl-carbamoyl]4-methoxybenzamide

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Chemical Property of N-[3-(4-methoxybenzylidene)-2-oxoindolin-6-yl-carbamoyl]4-methoxybenzamide

Chemical Property:

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Technology Process of N-[3-(4-methoxybenzylidene)-2-oxoindolin-6-yl-carbamoyl]4-methoxybenzamide

There total 6 articles about N-[3-(4-methoxybenzylidene)-2-oxoindolin-6-yl-carbamoyl]4-methoxybenzamide 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:

: 1621584-34-6
N-(2-oxoindolin-6-ylcarbamoyl)-4-methoxybenzamide

: 123-11-5
4-methoxy-benzaldehyde

: 1474049-13-2
(E)-4-methoxy-N-(3-(4-methoxybenzylidene)-2-oxoindolin-6-ylcarbamoyl)benzamide

: 1621584-54-0
N-[3-(4-methoxybenzylidene)-2-oxoindolin-6-yl-carbamoyl]4-methoxybenzamide

Guidance literature:: With pyrrolidine; In ethanol; at 100 ℃; for 0.25h; Overall yield = 68 %; Overall yield = 0.075 g; Microwave irradiation;
DOI:10.1016/j.ejmech.2014.07.108

Reference yield:

: 3424-93-9
4-methoxyphenylacetamide

: 1474049-13-2
(E)-4-methoxy-N-(3-(4-methoxybenzylidene)-2-oxoindolin-6-ylcarbamoyl)benzamide

: 1621584-54-0
N-[3-(4-methoxybenzylidene)-2-oxoindolin-6-yl-carbamoyl]4-methoxybenzamide

Guidance literature:: Multi-step reaction with 3 steps

1: dichloromethane / 40 °C

2: acetonitrile / 70 - 80 °C

3: pyrrolidine / ethanol / 0.25 h / 100 °C / Microwave irradiation

With pyrrolidine; In ethanol; dichloromethane; acetonitrile;
DOI:10.1016/j.ejmech.2014.07.108

Reference yield:

: 643-43-6
(2,4-dinitro-phenyl)-acetic acid

: 1474049-13-2
(E)-4-methoxy-N-(3-(4-methoxybenzylidene)-2-oxoindolin-6-ylcarbamoyl)benzamide

: 1621584-54-0
N-[3-(4-methoxybenzylidene)-2-oxoindolin-6-yl-carbamoyl]4-methoxybenzamide

Guidance literature:: Multi-step reaction with 4 steps

1: hydrogen; palladium on activated charcoal / methanol

2: hydrogenchloride / water / 6 h / Reflux

3: acetonitrile / 70 - 80 °C

4: pyrrolidine / ethanol / 0.25 h / 100 °C / Microwave irradiation

With pyrrolidine; hydrogenchloride; palladium on activated charcoal; hydrogen; In methanol; ethanol; water; acetonitrile;
DOI:10.1016/j.ejmech.2014.07.108