4-{[4-[[[N′-[(2-hydroxy-3-propylphenyl)methylene]-hydrazine]carbonyl]methyl ]-1-piperazinyl]methyl}-benzenesulfonamide

Base Information

Chemical Name:4-{[4-[[[N′-[(2-hydroxy-3-propylphenyl)methylene]-hydrazine]carbonyl]methyl ]-1-piperazinyl]methyl}-benzenesulfonamide
CAS No.:1554475-68-1
Molecular Formula:C₂₃H₃₁N₅O₄S
Molecular Weight:473.596
Hs Code.:

Synonyms:4-{[4-[[[N′-[(2-hydroxy-3-propylphenyl)methylene]-hydrazine]carbonyl]methyl ]-1-piperazinyl]methyl}-benzenesulfonamide

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Chemical Property of 4-{[4-[[[N′-[(2-hydroxy-3-propylphenyl)methylene]-hydrazine]carbonyl]methyl ]-1-piperazinyl]methyl}-benzenesulfonamide

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Technology Process of 4-{[4-[[[N′-[(2-hydroxy-3-propylphenyl)methylene]-hydrazine]carbonyl]methyl ]-1-piperazinyl]methyl}-benzenesulfonamide

There total 4 articles about 4-{[4-[[[N′-[(2-hydroxy-3-propylphenyl)methylene]-hydrazine]carbonyl]methyl ]-1-piperazinyl]methyl}-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: 89.0%

: 1239204-50-2
4-((4-(2-hydrazinyl-2-oxoethyl)piperazin-1-yl)methyl)benzenesulfonamide

: 83816-53-9
3-propyl-2-hydroxybenzaldehyde

: 1554475-68-1
4-{[4-[[[N′-[(2-hydroxy-3-propylphenyl)methylene]-hydrazine]carbonyl]methyl ]-1-piperazinyl]methyl}-benzenesulfonamide

Guidance literature:: With hydrogenchloride; In methanol; acetonitrile; Reflux;

Reference yield:

: 24019-66-7
3-allylsalicylaldehyde

: 1554475-68-1
4-{[4-[[[N′-[(2-hydroxy-3-propylphenyl)methylene]-hydrazine]carbonyl]methyl ]-1-piperazinyl]methyl}-benzenesulfonamide

Guidance literature:: Multi-step reaction with 2 steps

1: 5%-palladium/activated carbon; diphenyl sulfide; hydrogen / ethyl acetate / 20 °C

2: hydrogenchloride / methanol; acetonitrile / Reflux

With hydrogenchloride; diphenyl sulfide; 5%-palladium/activated carbon; hydrogen; In methanol; ethyl acetate; acetonitrile;

Reference yield:

: 90-02-8
salicylaldehyde

: 1554475-68-1
4-{[4-[[[N′-[(2-hydroxy-3-propylphenyl)methylene]-hydrazine]carbonyl]methyl ]-1-piperazinyl]methyl}-benzenesulfonamide

Guidance literature:: Multi-step reaction with 4 steps

1: potassium carbonate / N,N-dimethyl-formamide

2: neat (no solvent) / 200 °C

3: hydrogen; 5%-palladium/activated carbon; diphenyl sulfide / ethyl acetate / 20 °C

4: hydrogenchloride / water; methanol; acetonitrile / Reflux

With hydrogenchloride; diphenyl sulfide; 5%-palladium/activated carbon; hydrogen; potassium carbonate; In methanol; water; ethyl acetate; N,N-dimethyl-formamide; acetonitrile; 2: |Claisen Rearrangement;
DOI:10.1021/acs.jmedchem.5b00413