1-(3-nitrophenyl)-4-[1-(propane-2-sulfonyl)piperidin-4-ylmethyl]-4-piperazine

Base Information

Chemical Name:1-(3-nitrophenyl)-4-[1-(propane-2-sulfonyl)piperidin-4-ylmethyl]-4-piperazine
CAS No.:740873-59-0
Molecular Formula:C₁₉H₃₀N₄O₄S
Molecular Weight:410.538
Hs Code.:

Synonyms:1-(3-nitrophenyl)-4-[1-(propane-2-sulfonyl)piperidin-4-ylmethyl]-4-piperazine

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Chemical Property of 1-(3-nitrophenyl)-4-[1-(propane-2-sulfonyl)piperidin-4-ylmethyl]-4-piperazine

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Technology Process of 1-(3-nitrophenyl)-4-[1-(propane-2-sulfonyl)piperidin-4-ylmethyl]-4-piperazine

There total 7 articles about 1-(3-nitrophenyl)-4-[1-(propane-2-sulfonyl)piperidin-4-ylmethyl]-4-piperazine 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: 96.0%

: 1-(3-nitrophenyl)-4-piperidin-4-ylmethylpiperazine tris-trifluoroacetic acid salt

: 10147-37-2
Isopropylsulfonyl chloride

: 740873-59-0
1-(3-nitrophenyl)-4-[1-(propane-2-sulfonyl)piperidin-4-ylmethyl]-4-piperazine

Guidance literature:: With triethylamine; In dichloromethane; at 20 ℃; for 0.5h;
DOI:10.1021/jm0508641

Reference yield:

: 54054-85-2
1-(3-nitrophenyl)piperazine

: 740873-59-0
1-(3-nitrophenyl)-4-[1-(propane-2-sulfonyl)piperidin-4-ylmethyl]-4-piperazine

Guidance literature:: Multi-step reaction with 3 steps

1: 92 percent / Et₃N / tetrahydrofuran / 48 h / 20 °C

2: CH₂Cl₂ / 2 h / 0 °C

3: 96 percent / Et₃N / CH₂Cl₂ / 0.5 h / 20 °C

With triethylamine; In tetrahydrofuran; dichloromethane;
DOI:10.1021/jm0508641

Reference yield:

: 896125-05-6
4-[4-(3-nitrophenyl)piperazin-1-ylmethyl]piperidine-1-carboxylic acid tert-butyl ester

: 740873-59-0
1-(3-nitrophenyl)-4-[1-(propane-2-sulfonyl)piperidin-4-ylmethyl]-4-piperazine

Guidance literature:: Multi-step reaction with 2 steps

1: CH₂Cl₂ / 2 h / 0 °C

2: 96 percent / Et₃N / CH₂Cl₂ / 0.5 h / 20 °C

With triethylamine; In dichloromethane;
DOI:10.1021/jm0508641