N-(3-phenyl-3-[4-methanesulphonylpiperazin-1-yl]propyl)-4-[2-(4-methanesulphonylphenylsulphonyl)ethyl]-piperidine

Base Information

Chemical Name:N-(3-phenyl-3-[4-methanesulphonylpiperazin-1-yl]propyl)-4-[2-(4-methanesulphonylphenylsulphonyl)ethyl]-piperidine
CAS No.:718610-14-1
Molecular Formula:C₂₈H₄₁N₃O₆S₃
Molecular Weight:611.848
Hs Code.:

Synonyms:N-(3-phenyl-3-[4-methanesulphonylpiperazin-1-yl]propyl)-4-[2-(4-methanesulphonylphenylsulphonyl)ethyl]-piperidine

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Chemical Property of N-(3-phenyl-3-[4-methanesulphonylpiperazin-1-yl]propyl)-4-[2-(4-methanesulphonylphenylsulphonyl)ethyl]-piperidine

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Technology Process of N-(3-phenyl-3-[4-methanesulphonylpiperazin-1-yl]propyl)-4-[2-(4-methanesulphonylphenylsulphonyl)ethyl]-piperidine

There total 7 articles about N-(3-phenyl-3-[4-methanesulphonylpiperazin-1-yl]propyl)-4-[2-(4-methanesulphonylphenylsulphonyl)ethyl]-piperidine 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:

: 55276-43-2
4-methanesulfonylpiperazine

: 718610-15-2
N-(3-phenyl-3-chloropropyl)-4-[2-(4-methanesulphonylphenylsulphonyl)ethyl]-piperidine

: 718610-14-1
N-(3-phenyl-3-[4-methanesulphonylpiperazin-1-yl]propyl)-4-[2-(4-methanesulphonylphenylsulphonyl)ethyl]-piperidine

Guidance literature:: With triethylamine; In dichloromethane; at 20 ℃; for 16h;

Reference yield:

: 1122-97-0
4-methylsulfanyl-thiophenol

: 718610-14-1
N-(3-phenyl-3-[4-methanesulphonylpiperazin-1-yl]propyl)-4-[2-(4-methanesulphonylphenylsulphonyl)ethyl]-piperidine

Guidance literature:: Multi-step reaction with 7 steps

1.1: sodium hydride / DMF (N,N-dimethyl-formamide) / 0.5 h / 0 °C

1.2: 16 h / 20 °C

2.1: 3-chloro-benzenecarboperoxoic acid / dichloromethane / 16 h / 0 - 20 °C

3.1: trifluoroacetic acid / dichloromethane / 1 h / 20 °C

4.1: potassium carbonate / DMF (N,N-dimethyl-formamide) / 1 h / 20 °C

5.1: sodium tetrahydroborate / ethanol / 18 h / 20 °C

6.1: methanesulfonyl chloride; triethylamine / dichloromethane / 18 h / 20 °C

7.1: triethylamine / dichloromethane / 16 h / 20 °C

With sodium tetrahydroborate; sodium hydride; potassium carbonate; methanesulfonyl chloride; triethylamine; 3-chloro-benzenecarboperoxoic acid; trifluoroacetic acid; In DMF (N,N-dimethyl-formamide); ethanol; dichloromethane;

Reference yield:

: 718610-26-5
4-(2-[4-methanesulphonylphenylsulphonyl]ethyl)piperidine

: 718610-14-1
N-(3-phenyl-3-[4-methanesulphonylpiperazin-1-yl]propyl)-4-[2-(4-methanesulphonylphenylsulphonyl)ethyl]-piperidine

Guidance literature:: Multi-step reaction with 4 steps

1: potassium carbonate / DMF (N,N-dimethyl-formamide) / 1 h / 20 °C

2: sodium tetrahydroborate / ethanol / 18 h / 20 °C

3: methanesulfonyl chloride; triethylamine / dichloromethane / 18 h / 20 °C

4: triethylamine / dichloromethane / 16 h / 20 °C

With sodium tetrahydroborate; potassium carbonate; methanesulfonyl chloride; triethylamine; In DMF (N,N-dimethyl-formamide); ethanol; dichloromethane;