4-((4-(3-amino-6-(4-cyano-2,6-dimethylphenoxy)pyridin-2-ylamino)piperidin-1-yl)methyl)benzenesulfonamide

Base Information

Chemical Name:4-((4-(3-amino-6-(4-cyano-2,6-dimethylphenoxy)pyridin-2-ylamino)piperidin-1-yl)methyl)benzenesulfonamide
CAS No.:1421045-02-4
Molecular Formula:C₂₆H₃₀N₆O₃S
Molecular Weight:506.629
Hs Code.:

Synonyms:4-((4-(3-amino-6-(4-cyano-2,6-dimethylphenoxy)pyridin-2-ylamino)piperidin-1-yl)methyl)benzenesulfonamide

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Chemical Property of 4-((4-(3-amino-6-(4-cyano-2,6-dimethylphenoxy)pyridin-2-ylamino)piperidin-1-yl)methyl)benzenesulfonamide

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Technology Process of 4-((4-(3-amino-6-(4-cyano-2,6-dimethylphenoxy)pyridin-2-ylamino)piperidin-1-yl)methyl)benzenesulfonamide

There total 6 articles about 4-((4-(3-amino-6-(4-cyano-2,6-dimethylphenoxy)pyridin-2-ylamino)piperidin-1-yl)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: 46.0%

: 1421045-21-7
6-(4-cyano-2,6-dimethylphenoxy)-N²-(piperidin-4-yl)pyridine-2,3-diamine

: 102153-43-5
4-(chloromethyl)benzenesulfonamide

: 1421045-02-4
4-((4-(3-amino-6-(4-cyano-2,6-dimethylphenoxy)pyridin-2-ylamino)piperidin-1-yl)methyl)benzenesulfonamide

Guidance literature:: With potassium carbonate; In acetone; at 0 - 20 ℃;
DOI:10.1002/cmdc.201300130

Reference yield:

: 1421045-19-3
6-(4-cyano-2,6-dimethylphenoxy)-N²-(1-Boc-piperidin-4-yl)pyridine-2,3-diamine

: 1421045-02-4
4-((4-(3-amino-6-(4-cyano-2,6-dimethylphenoxy)pyridin-2-ylamino)piperidin-1-yl)methyl)benzenesulfonamide

Guidance literature:: Multi-step reaction with 2 steps

1: trifluoroacetic acid / dichloromethane / 20 °C

2: potassium carbonate / acetone / 0 - 20 °C

With potassium carbonate; trifluoroacetic acid; In dichloromethane; acetone;
DOI:10.1002/cmdc.201300130

Reference yield:

: 400801-28-7
(6-chloro-3-nitropyridin-2-yl)-(1-Boc-piperidin-4-yl)amine

: 1421045-02-4
4-((4-(3-amino-6-(4-cyano-2,6-dimethylphenoxy)pyridin-2-ylamino)piperidin-1-yl)methyl)benzenesulfonamide

Guidance literature:: Multi-step reaction with 4 steps

1.1: caesium carbonate / 1,4-dioxane / 0.25 h / 20 °C

1.2: 7 h / Reflux

2.1: palladium 10% on activated carbon; hydrogen / methanol / 20 °C

3.1: trifluoroacetic acid / dichloromethane / 20 °C

4.1: potassium carbonate / acetone / 0 - 20 °C

With palladium 10% on activated carbon; hydrogen; potassium carbonate; caesium carbonate; trifluoroacetic acid; In 1,4-dioxane; methanol; dichloromethane; acetone;
DOI:10.1002/cmdc.201300130