N-[(7-cyano-2-napthyl)methyl]-N-[4-(4-cyanopiperidin-1-yl)phenyl]methanesulfonamide

Base Information

Chemical Name:N-[(7-cyano-2-napthyl)methyl]-N-[4-(4-cyanopiperidin-1-yl)phenyl]methanesulfonamide
CAS No.:714249-03-3
Molecular Formula:C₂₅H₂₄N₄O₂S
Molecular Weight:444.557
Hs Code.:

Synonyms:N-[(7-cyano-2-napthyl)methyl]-N-[4-(4-cyanopiperidin-1-yl)phenyl]methanesulfonamide

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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-[(7-cyano-2-napthyl)methyl]-N-[4-(4-cyanopiperidin-1-yl)phenyl]methanesulfonamide

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Technology Process of N-[(7-cyano-2-napthyl)methyl]-N-[4-(4-cyanopiperidin-1-yl)phenyl]methanesulfonamide

There total 3 articles about N-[(7-cyano-2-napthyl)methyl]-N-[4-(4-cyanopiperidin-1-yl)phenyl]methanesulfonamide 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: 90.0%

: 124-63-0
methanesulfonyl chloride

: 714248-92-7
1-(4-{[(7-cyano-2-naphthyl)methyl]amino}phenyl)piperidine-4-carboxamide

: 714249-03-3
N-[(7-cyano-2-napthyl)methyl]-N-[4-(4-cyanopiperidin-1-yl)phenyl]methanesulfonamide

Guidance literature:: With pyridine; In 1,2-dichloro-ethane; at 20 ℃; for 12h;
DOI:10.1016/j.bmc.2004.02.022

Reference yield:

: 39546-32-2
4-carboxamidopiperidine

: 714249-03-3
N-[(7-cyano-2-napthyl)methyl]-N-[4-(4-cyanopiperidin-1-yl)phenyl]methanesulfonamide

Guidance literature:: Multi-step reaction with 4 steps

1: 87 percent / potassium carbonate / dimethylformamide / 13 h / 90 °C

2: H₂ / Pd/C / ethanol / 16 h / 20 °C

3: acetic acid; sodium triacetoxyborohydride / 1,2-dichloro-ethane / 5 h

4: 90 percent / pyridine / 1,2-dichloro-ethane / 12 h / 20 °C

With pyridine; hydrogen; sodium tris(acetoxy)borohydride; potassium carbonate; acetic acid; palladium on activated charcoal; In ethanol; 1,2-dichloro-ethane; N,N-dimethyl-formamide;
DOI:10.1016/j.bmc.2004.02.022

Reference yield:

: 223786-50-3
1-(4-amino-phenyl)-piperidine-4-carboxylic acid amide

: 714249-03-3
N-[(7-cyano-2-napthyl)methyl]-N-[4-(4-cyanopiperidin-1-yl)phenyl]methanesulfonamide

Guidance literature:: Multi-step reaction with 2 steps

1: acetic acid; sodium triacetoxyborohydride / 1,2-dichloro-ethane / 5 h

2: 90 percent / pyridine / 1,2-dichloro-ethane / 12 h / 20 °C

With pyridine; sodium tris(acetoxy)borohydride; acetic acid; In 1,2-dichloro-ethane;
DOI:10.1016/j.bmc.2004.02.022