1-cyclohexyl-N-(4-(4-(6-nitropyridin-2-yl)piperazin-1-yl)butyl)methane-sulfonamide

Base Information

Chemical Name:1-cyclohexyl-N-(4-(4-(6-nitropyridin-2-yl)piperazin-1-yl)butyl)methane-sulfonamide
CAS No.:1351412-08-2
Molecular Formula:C₂₀H₃₃N₅O₄S
Molecular Weight:439.579
Hs Code.:

Synonyms:1-cyclohexyl-N-(4-(4-(6-nitropyridin-2-yl)piperazin-1-yl)butyl)methane-sulfonamide

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Chemical Property of 1-cyclohexyl-N-(4-(4-(6-nitropyridin-2-yl)piperazin-1-yl)butyl)methane-sulfonamide

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Technology Process of 1-cyclohexyl-N-(4-(4-(6-nitropyridin-2-yl)piperazin-1-yl)butyl)methane-sulfonamide

There total 7 articles about 1-cyclohexyl-N-(4-(4-(6-nitropyridin-2-yl)piperazin-1-yl)butyl)methane-sulfonamide 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: 44.0%

: 1351412-10-6
4-(4-(6-nitropyridin-2-yl)piperazin-1-yl)butan-1-amine

: 4352-30-1
cyclohexylmethylsulfonyl chloride

: 1351412-08-2
1-cyclohexyl-N-(4-(4-(6-nitropyridin-2-yl)piperazin-1-yl)butyl)methane-sulfonamide

Guidance literature:: With triethylamine; In dichloromethane; at 20 ℃; for 4h; Inert atmosphere;

Reference yield: 26.0%

: 1351412-07-1
1-cyclohexyl-N-(4-(piperazin-1-yl)butyl)methanesulfonamide

: 94166-64-0
2-nitro-6-chloro-pyridine

: 1351412-08-2
1-cyclohexyl-N-(4-(4-(6-nitropyridin-2-yl)piperazin-1-yl)butyl)methane-sulfonamide

Guidance literature:: With N-ethyl-N,N-diisopropylamine; In acetonitrile; at 130 ℃; for 0.666667h;

Reference yield:

: 745048-06-0
4-[4-(1,3-dioxo-1,3-dihydroisoindol-2-yl)butyl]piperazine-1-carboxylic acid tert-butyl ester

: 1351412-08-2
1-cyclohexyl-N-(4-(4-(6-nitropyridin-2-yl)piperazin-1-yl)butyl)methane-sulfonamide

Guidance literature:: Multi-step reaction with 4 steps

1: hydrazine hydrate / ethanol / 18 h / 20 - 90 °C / Inert atmosphere

2: N-ethyl-N,N-diisopropylamine / dichloromethane / 18 h / 20 °C

3: trifluoroacetic acid / dichloromethane / 0.25 h

4: N-ethyl-N,N-diisopropylamine / acetonitrile / 0.67 h / 130 °C

With hydrazine hydrate; N-ethyl-N,N-diisopropylamine; trifluoroacetic acid; In ethanol; dichloromethane; acetonitrile;