N-[1-(3-Cyano-benzyl)-2-oxo-2-piperidin-1-yl-ethyl]-4-methyl-benzenesulfonamide

Base Information

Chemical Name:N-[1-(3-Cyano-benzyl)-2-oxo-2-piperidin-1-yl-ethyl]-4-methyl-benzenesulfonamide
CAS No.:80852-53-5
Molecular Formula:C₂₂H₂₅N₃O₃S
Molecular Weight:411.525
Hs Code.:

Synonyms:N-[1-(3-Cyano-benzyl)-2-oxo-2-piperidin-1-yl-ethyl]-4-methyl-benzenesulfonamide

Suppliers and Price of N-[1-(3-Cyano-benzyl)-2-oxo-2-piperidin-1-yl-ethyl]-4-methyl-benzenesulfonamide

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of N-[1-(3-Cyano-benzyl)-2-oxo-2-piperidin-1-yl-ethyl]-4-methyl-benzenesulfonamide

Chemical Property:

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Technology Process of N-[1-(3-Cyano-benzyl)-2-oxo-2-piperidin-1-yl-ethyl]-4-methyl-benzenesulfonamide

There total 5 articles about N-[1-(3-Cyano-benzyl)-2-oxo-2-piperidin-1-yl-ethyl]-4-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: 42.0%

: 110-89-4
piperidine

: 80852-49-9
3-(3-Cyano-phenyl)-2-(toluene-4-sulfonylamino)-propionyl chloride

: 80852-53-5
N-[1-(3-Cyano-benzyl)-2-oxo-2-piperidin-1-yl-ethyl]-4-methyl-benzenesulfonamide

Guidance literature:: In benzene; for 1.5h; Ambient temperature;

Reference yield:

: 52117-00-7
2-Acetylamino-2-[(3-cyanophenyl)-methyl]-malonic acid diethyl ester

: 80852-53-5
N-[1-(3-Cyano-benzyl)-2-oxo-2-piperidin-1-yl-ethyl]-4-methyl-benzenesulfonamide

Guidance literature:: Multi-step reaction with 3 steps

1: 1.) 3 M HCl, 2.) 1 M KOH / 1.) acetic acid, 6 h, reflux, 2.) ether, 12 h, r.t.

2: SOCl₂ / 1 h / Heating

3: 42 percent / benzene / 1.5 h / Ambient temperature

With hydrogenchloride; potassium hydroxide; thionyl chloride; In benzene;

Reference yield:

: 98-59-9
p-toluenesulfonyl chloride

: 80852-53-5
N-[1-(3-Cyano-benzyl)-2-oxo-2-piperidin-1-yl-ethyl]-4-methyl-benzenesulfonamide

Guidance literature:: Multi-step reaction with 3 steps

1: 1.) 3 M HCl, 2.) 1 M KOH / 1.) acetic acid, 6 h, reflux, 2.) ether, 12 h, r.t.

2: SOCl₂ / 1 h / Heating

3: 42 percent / benzene / 1.5 h / Ambient temperature

With hydrogenchloride; potassium hydroxide; thionyl chloride; In benzene;