N-(4-formylbenzyl)-N-(1-(5-nitropyridin-2-yl)piperidin-4-yl)methanesulfonamide

Base Information

Chemical Name:N-(4-formylbenzyl)-N-(1-(5-nitropyridin-2-yl)piperidin-4-yl)methanesulfonamide
CAS No.:1404097-63-7
Molecular Formula:C₁₉H₂₂N₄O₅S
Molecular Weight:418.473
Hs Code.:

Synonyms:N-(4-formylbenzyl)-N-(1-(5-nitropyridin-2-yl)piperidin-4-yl)methanesulfonamide

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Chemical Property of N-(4-formylbenzyl)-N-(1-(5-nitropyridin-2-yl)piperidin-4-yl)methanesulfonamide

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Technology Process of N-(4-formylbenzyl)-N-(1-(5-nitropyridin-2-yl)piperidin-4-yl)methanesulfonamide

There total 5 articles about N-(4-formylbenzyl)-N-(1-(5-nitropyridin-2-yl)piperidin-4-yl)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: 69.4%

: 1404097-62-6
4-(((1-(5-nitropyridin-2-yl)piperidin-4-yl)amino)methyl)benzaldehyde

: 124-63-0
methanesulfonyl chloride

: 1404097-63-7
N-(4-formylbenzyl)-N-(1-(5-nitropyridin-2-yl)piperidin-4-yl)methanesulfonamide

Guidance literature:: With triethylamine; In dichloromethane; at 20 - 25 ℃;
DOI:10.1021/jm301164y

Reference yield:

: C₁₀H₁₄N₄O₂*C₂HF₃O₂

: 1404097-63-7
N-(4-formylbenzyl)-N-(1-(5-nitropyridin-2-yl)piperidin-4-yl)methanesulfonamide

Guidance literature:: Multi-step reaction with 4 steps

1: potassium carbonate / ethanol; water / 25 - 80 °C

2: sodium tetrahydroborate / methanol / 0.5 h / 0 - 60 °C

3: hydrogenchloride / water; acetone / 0.5 h

4: triethylamine / dichloromethane / 20 - 25 °C

With hydrogenchloride; sodium tetrahydroborate; potassium carbonate; triethylamine; In methanol; ethanol; dichloromethane; water; acetone;
DOI:10.1021/jm301164y

Reference yield:

: 4548-45-2
2-chloro-5-nitropyridine

: 1404097-63-7
N-(4-formylbenzyl)-N-(1-(5-nitropyridin-2-yl)piperidin-4-yl)methanesulfonamide

Guidance literature:: Multi-step reaction with 6 steps

1: potassium carbonate / N,N-dimethyl-formamide / 4 h / 80 °C

2: dichloromethane / 3 h / 0 - 25 °C

3: potassium carbonate / ethanol; water / 25 - 80 °C

4: sodium tetrahydroborate / methanol / 0.5 h / 0 - 60 °C

5: hydrogenchloride / water; acetone / 0.5 h

6: triethylamine / dichloromethane / 20 - 25 °C

With hydrogenchloride; sodium tetrahydroborate; potassium carbonate; triethylamine; In methanol; ethanol; dichloromethane; water; N,N-dimethyl-formamide; acetone;
DOI:10.1021/jm301164y