(Z)-5-((6-(3-(4-methoxyphenylamino)-3-oxopropanamido)-2-oxoindolin-3-ylidene)methyl)-2,4-dimethyl-1H-pyrrole-3-carboxylic acid

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Chemical Name:(Z)-5-((6-(3-(4-methoxyphenylamino)-3-oxopropanamido)-2-oxoindolin-3-ylidene)methyl)-2,4-dimethyl-1H-pyrrole-3-carboxylic acid
CAS No.:1621689-59-5
Molecular Formula:C₂₆H₂₄N₄O₆
Molecular Weight:488.5
Hs Code.:

Synonyms:(Z)-5-((6-(3-(4-methoxyphenylamino)-3-oxopropanamido)-2-oxoindolin-3-ylidene)methyl)-2,4-dimethyl-1H-pyrrole-3-carboxylic acid

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Chemical Property of (Z)-5-((6-(3-(4-methoxyphenylamino)-3-oxopropanamido)-2-oxoindolin-3-ylidene)methyl)-2,4-dimethyl-1H-pyrrole-3-carboxylic acid

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Technology Process of (Z)-5-((6-(3-(4-methoxyphenylamino)-3-oxopropanamido)-2-oxoindolin-3-ylidene)methyl)-2,4-dimethyl-1H-pyrrole-3-carboxylic acid

There total 4 articles about (Z)-5-((6-(3-(4-methoxyphenylamino)-3-oxopropanamido)-2-oxoindolin-3-ylidene)methyl)-2,4-dimethyl-1H-pyrrole-3-carboxylic acid 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:

: 253870-02-9
5-formyl-2,4-dimethyl-1H-pyrrole-3-carboxylic acid

: 1621689-23-3
N¹-(4-methoxyphenyl)-N³-(2-oxoindolin-6-yl)malonamide

: 1621689-59-5
(Z)-5-((6-(3-(4-methoxyphenylamino)-3-oxopropanamido)-2-oxoindolin-3-ylidene)methyl)-2,4-dimethyl-1H-pyrrole-3-carboxylic acid

Guidance literature:: With pyrrolidine; In ethanol; at 100 ℃; Microwave irradiation;
DOI:10.1016/j.ejmech.2014.07.033

Reference yield:

: 61916-60-7
3-((4-methoxyphenyl)amino)-3-oxopropanoic acid

: 1621689-59-5
(Z)-5-((6-(3-(4-methoxyphenylamino)-3-oxopropanamido)-2-oxoindolin-3-ylidene)methyl)-2,4-dimethyl-1H-pyrrole-3-carboxylic acid

Guidance literature:: Multi-step reaction with 2 steps

1: triethylamine; O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate / N,N-dimethyl-formamide; acetonitrile / 3 h / 20 °C

2: pyrrolidine / ethanol / 100 °C / Microwave irradiation

With pyrrolidine; O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate; triethylamine; In ethanol; N,N-dimethyl-formamide; acetonitrile; 2: |Aldol Condensation;
DOI:10.1016/j.ejmech.2014.07.033

Reference yield:

: 104-94-9
4-methoxy-aniline

: 1621689-59-5
(Z)-5-((6-(3-(4-methoxyphenylamino)-3-oxopropanamido)-2-oxoindolin-3-ylidene)methyl)-2,4-dimethyl-1H-pyrrole-3-carboxylic acid

Guidance literature:: Multi-step reaction with 4 steps

1: triethylamine / dichloromethane / 4 h / 0 °C

2: sodium hydroxide; water / ethanol / 1.5 h / Reflux

3: triethylamine; O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate / N,N-dimethyl-formamide; acetonitrile / 3 h / 20 °C

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

With pyrrolidine; water; O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate; triethylamine; sodium hydroxide; In ethanol; dichloromethane; N,N-dimethyl-formamide; acetonitrile; 4: |Aldol Condensation;
DOI:10.1016/j.ejmech.2014.07.033