N-methyl-4-{2-[(methyloxy)methyl]-1-piperidinyl}-3-nitrobenzenesulfonamide

Base Information

Chemical Name:N-methyl-4-{2-[(methyloxy)methyl]-1-piperidinyl}-3-nitrobenzenesulfonamide
CAS No.:1351094-47-7
Molecular Formula:C₁₄H₂₁N₃O₅S
Molecular Weight:343.404
Hs Code.:

Synonyms:N-methyl-4-{2-[(methyloxy)methyl]-1-piperidinyl}-3-nitrobenzenesulfonamide

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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-methyl-4-{2-[(methyloxy)methyl]-1-piperidinyl}-3-nitrobenzenesulfonamide

Chemical Property:

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Technology Process of N-methyl-4-{2-[(methyloxy)methyl]-1-piperidinyl}-3-nitrobenzenesulfonamide

There total 6 articles about N-methyl-4-{2-[(methyloxy)methyl]-1-piperidinyl}-3-nitrobenzenesulfonamide 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: 74.0%

: 688809-98-5
2-[(methyloxy)methyl]piperidine hydrochloride

: 1041598-53-1
4-fluoro-N-methyl-3-nitrobenzenesulfonamide

: 1351094-47-7
N-methyl-4-{2-[(methyloxy)methyl]-1-piperidinyl}-3-nitrobenzenesulfonamide

Guidance literature:: With triethylamine; at 110 ℃; for 20h; Sealed vessel;

Reference yield:

: 3433-37-2
piperidin-2-ylmethanol

: 1351094-47-7
N-methyl-4-{2-[(methyloxy)methyl]-1-piperidinyl}-3-nitrobenzenesulfonamide

Guidance literature:: Multi-step reaction with 4 steps

1.1: acetonitrile / 20 h / 25 °C

2.1: sodium hydride / tetrahydrofuran; mineral oil / 1 h / 25 °C

2.2: 20 h / 20 °C

3.1: hydrogenchloride / dichloromethane; 1,4-dioxane / 20 h / 25 °C

4.1: triethylamine / 20 h / 110 °C / Sealed vessel

With hydrogenchloride; sodium hydride; triethylamine; In tetrahydrofuran; 1,4-dioxane; dichloromethane; acetonitrile; mineral oil;

Reference yield:

: 6668-56-0
4-fluoro-3-nitrobenzene-1-sulfonyl chloride

: 1351094-47-7
N-methyl-4-{2-[(methyloxy)methyl]-1-piperidinyl}-3-nitrobenzenesulfonamide

Guidance literature:: Multi-step reaction with 2 steps

1: triethylamine / tetrahydrofuran / 1 h / -35 °C

2: triethylamine / 20 h / 110 °C / Sealed vessel

With triethylamine; In tetrahydrofuran;