3-amino-4-[2-(hydroxymethyl)-1-piperidinyl]-N-methylbenzenesulfonamide

Base Information

Chemical Name:3-amino-4-[2-(hydroxymethyl)-1-piperidinyl]-N-methylbenzenesulfonamide
CAS No.:1304981-00-7
Molecular Formula:C₁₃H₂₁N₃O₃S
Molecular Weight:299.394
Hs Code.:

Synonyms:3-amino-4-[2-(hydroxymethyl)-1-piperidinyl]-N-methylbenzenesulfonamide

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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 3-amino-4-[2-(hydroxymethyl)-1-piperidinyl]-N-methylbenzenesulfonamide

Chemical Property:

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Technology Process of 3-amino-4-[2-(hydroxymethyl)-1-piperidinyl]-N-methylbenzenesulfonamide

There total 4 articles about 3-amino-4-[2-(hydroxymethyl)-1-piperidinyl]-N-methylbenzenesulfonamide 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: 85.0%

: 1351094-19-3
4-[2-(hydroxymethyl)-1-piperidinyl]-N-methyl-3-nitrobenzenesulfonamide

: 1304981-00-7
3-amino-4-[2-(hydroxymethyl)-1-piperidinyl]-N-methylbenzenesulfonamide

Guidance literature:: With hydrogen; palladium on activated charcoal; In ethanol; at 20 ℃; for 0.666667h; under 1810.07 Torr;

Reference yield:

: 1493-27-2,127723-77-7
ortho-nitrofluorobenzene

: 1304981-00-7
3-amino-4-[2-(hydroxymethyl)-1-piperidinyl]-N-methylbenzenesulfonamide

Guidance literature:: Multi-step reaction with 4 steps

1: chlorosulfonic acid / 18 h / 100 °C

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

3: 1,4-dioxane / 20 h / 100 °C

4: hydrogen / palladium on activated charcoal / ethanol / 0.67 h / 20 °C / 1810.07 Torr

With chlorosulfonic acid; hydrogen; triethylamine; palladium on activated charcoal; In tetrahydrofuran; 1,4-dioxane; ethanol;

Reference yield:

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

: 1304981-00-7
3-amino-4-[2-(hydroxymethyl)-1-piperidinyl]-N-methylbenzenesulfonamide

Guidance literature:: Multi-step reaction with 3 steps

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

2: 1,4-dioxane / 20 h / 100 °C

3: hydrogen / palladium on activated charcoal / ethanol / 0.67 h / 20 °C / 1810.07 Torr

With hydrogen; triethylamine; palladium on activated charcoal; In tetrahydrofuran; 1,4-dioxane; ethanol;