N-(1-indanyl)-4-{N-methyl-N-[(E)-3-(3,4-dihydroxyphenyl)-2-propenoyl]amino}benzenesulfonamide

Base Information

Chemical Name:N-(1-indanyl)-4-{N-methyl-N-[(E)-3-(3,4-dihydroxyphenyl)-2-propenoyl]amino}benzenesulfonamide
CAS No.:134907-28-1
Molecular Formula:C₂₅H₂₄N₂O₅S
Molecular Weight:464.542
Hs Code.:

Synonyms:N-(1-indanyl)-4-{N-methyl-N-[(E)-3-(3,4-dihydroxyphenyl)-2-propenoyl]amino}benzenesulfonamide

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Chemical Property of N-(1-indanyl)-4-{N-methyl-N-[(E)-3-(3,4-dihydroxyphenyl)-2-propenoyl]amino}benzenesulfonamide

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Technology Process of N-(1-indanyl)-4-{N-methyl-N-[(E)-3-(3,4-dihydroxyphenyl)-2-propenoyl]amino}benzenesulfonamide

There total 6 articles about N-(1-indanyl)-4-{N-methyl-N-[(E)-3-(3,4-dihydroxyphenyl)-2-propenoyl]amino}benzenesulfonamide 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:

: 77201-71-9
(E)-3-(3,4-dihydroxyphenyl)acryloyl chloride

: 134907-53-2
N-(1-Indanyl)-4-(methylamino)benzenesulfonamide

: 134907-28-1
N-(1-indanyl)-4-{N-methyl-N-[(E)-3-(3,4-dihydroxyphenyl)-2-propenoyl]amino}benzenesulfonamide

Guidance literature:: In pyridine; dichloromethane; at 0 - 20 ℃; for 2h;

Reference yield:

: Acetic acid 2-acetoxy-5-((E)-2-{[4-(indan-1-ylsulfamoyl)-phenyl]-methyl-carbamoyl}-vinyl)-phenyl ester

: 134907-28-1
N-(1-indanyl)-4-{N-methyl-N-[(E)-3-(3,4-dihydroxyphenyl)-2-propenoyl]amino}benzenesulfonamide

Guidance literature:: With hydrogenchloride; In tetrahydrofuran; at 60 ℃; for 0.333333h; Yield given;
DOI:10.1021/jm00111a048

Reference yield:

: 34698-41-4
2,3-dihydro-1H-inden-1-amine

: 134907-28-1
N-(1-indanyl)-4-{N-methyl-N-[(E)-3-(3,4-dihydroxyphenyl)-2-propenoyl]amino}benzenesulfonamide

Guidance literature:: Multi-step reaction with 4 steps

1: CH₃COONa / ethanol / 4 h / Ambient temperature

2: 1 N aq. NaOH / ethanol / Heating

3: pyridine / CH₂Cl₂ / 2 h / Ambient temperature

4: methanolic 2 N HCl / tetrahydrofuran / 0.33 h / 60 °C

With pyridine; hydrogenchloride; sodium hydroxide; sodium acetate; In tetrahydrofuran; ethanol; dichloromethane;
DOI:10.1021/jm00111a048