1-(4-acryloylamino-benzenesulfonyl)-piperidine-4-carboxylic acid dimethylamide

Base Information

Chemical Name:1-(4-acryloylamino-benzenesulfonyl)-piperidine-4-carboxylic acid dimethylamide
CAS No.:1306722-18-8
Molecular Formula:C₁₇H₂₃N₃O₄S
Molecular Weight:365.453
Hs Code.:

Synonyms:1-(4-acryloylamino-benzenesulfonyl)-piperidine-4-carboxylic acid dimethylamide

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Chemical Property of 1-(4-acryloylamino-benzenesulfonyl)-piperidine-4-carboxylic acid dimethylamide

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Technology Process of 1-(4-acryloylamino-benzenesulfonyl)-piperidine-4-carboxylic acid dimethylamide

There total 7 articles about 1-(4-acryloylamino-benzenesulfonyl)-piperidine-4-carboxylic acid dimethylamide 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: 15.0%

: 1306723-13-6
1-(4-amino-benzenesulfonyl)-piperidine-4-carboxylic acid dimethylamide

: 814-68-6,25189-84-8
acryloyl chloride

: 1306722-18-8
1-(4-acryloylamino-benzenesulfonyl)-piperidine-4-carboxylic acid dimethylamide

Guidance literature:: With N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; at 20 ℃; for 1h; Inert atmosphere;

Reference yield:

: 98-74-8
4-Nitrobenzenesulfonyl chloride

: 1306722-18-8
1-(4-acryloylamino-benzenesulfonyl)-piperidine-4-carboxylic acid dimethylamide

Guidance literature:: Multi-step reaction with 6 steps

1: N-ethyl-N,N-diisopropylamine / tetrahydrofuran / 18 h / 20 °C / Inert atmosphere

2: water; lithium hydroxide / tetrahydrofuran / 2 h / 20 °C

3: thionyl chloride / toluene / 2 h / 80 °C

4: N-ethyl-N,N-diisopropylamine / dichloromethane / 18 h / 20 °C / Inert atmosphere

5: ammonium chloride; iron / ethanol; water / 18 h / 20 °C

6: N-ethyl-N,N-diisopropylamine / tetrahydrofuran / 1 h / 20 °C / Inert atmosphere

With thionyl chloride; water; iron; ammonium chloride; N-ethyl-N,N-diisopropylamine; lithium hydroxide; In tetrahydrofuran; ethanol; dichloromethane; water; toluene;

Reference yield:

: 2971-79-1
isonipecotic acid methyl ester

: 1306722-18-8
1-(4-acryloylamino-benzenesulfonyl)-piperidine-4-carboxylic acid dimethylamide

Guidance literature:: Multi-step reaction with 6 steps

1: N-ethyl-N,N-diisopropylamine / tetrahydrofuran / 18 h / 20 °C / Inert atmosphere

2: water; lithium hydroxide / tetrahydrofuran / 2 h / 20 °C

3: thionyl chloride / toluene / 2 h / 80 °C

4: N-ethyl-N,N-diisopropylamine / dichloromethane / 18 h / 20 °C / Inert atmosphere

5: ammonium chloride; iron / ethanol; water / 18 h / 20 °C

6: N-ethyl-N,N-diisopropylamine / tetrahydrofuran / 1 h / 20 °C / Inert atmosphere

With thionyl chloride; water; iron; ammonium chloride; N-ethyl-N,N-diisopropylamine; lithium hydroxide; In tetrahydrofuran; ethanol; dichloromethane; water; toluene;