5-chloro-thiophene-2-carboxylic acid [(S)-2-(3-bromo-2-methyl-benzenesulfonyl-amino)-3-(4-methyl-piperazin-1-yl)-3-oxo-propyl]-amide

Base Information

Chemical Name:5-chloro-thiophene-2-carboxylic acid [(S)-2-(3-bromo-2-methyl-benzenesulfonyl-amino)-3-(4-methyl-piperazin-1-yl)-3-oxo-propyl]-amide
CAS No.:1184298-47-2
Molecular Formula:C₂₀H₂₄BrClN₄O₄S₂
Molecular Weight:563.924
Hs Code.:

Synonyms:5-chloro-thiophene-2-carboxylic acid [(S)-2-(3-bromo-2-methyl-benzenesulfonyl-amino)-3-(4-methyl-piperazin-1-yl)-3-oxo-propyl]-amide

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Chemical Property of 5-chloro-thiophene-2-carboxylic acid [(S)-2-(3-bromo-2-methyl-benzenesulfonyl-amino)-3-(4-methyl-piperazin-1-yl)-3-oxo-propyl]-amide

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Technology Process of 5-chloro-thiophene-2-carboxylic acid [(S)-2-(3-bromo-2-methyl-benzenesulfonyl-amino)-3-(4-methyl-piperazin-1-yl)-3-oxo-propyl]-amide

There total 8 articles about 5-chloro-thiophene-2-carboxylic acid [(S)-2-(3-bromo-2-methyl-benzenesulfonyl-amino)-3-(4-methyl-piperazin-1-yl)-3-oxo-propyl]-amide 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: 80.0%

: 886501-61-7
3-bromo-2-methylbenzene-1-sulfonyl chloride

: 5-chloro-thiophene-2-carboxylic acid [(S)-2-amino-3-(4-methyl-piperazin-1-yl)-3-oxo-propyl]-amide dihydrochloride

: 1184298-47-2
5-chloro-thiophene-2-carboxylic acid [(S)-2-(3-bromo-2-methyl-benzenesulfonyl-amino)-3-(4-methyl-piperazin-1-yl)-3-oxo-propyl]-amide

Guidance literature:: With triethylamine; In dichloromethane; at 0 ℃;

Reference yield:

: 69321-60-4
2,6-dibromotoluene

: 1184298-47-2
5-chloro-thiophene-2-carboxylic acid [(S)-2-(3-bromo-2-methyl-benzenesulfonyl-amino)-3-(4-methyl-piperazin-1-yl)-3-oxo-propyl]-amide

Guidance literature:: Multi-step reaction with 3 steps

1: N-ethyl-N,N-diisopropylamine / tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene / 1,4-dioxane / 100 °C / Inert atmosphere

2: sulfuryl dichloride; water; acetic acid / dichloromethane / 0.42 h / 0 - 20 °C

3: triethylamine / dichloromethane / 0 °C

With sulfuryl dichloride; water; acetic acid; triethylamine; N-ethyl-N,N-diisopropylamine; tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene; In 1,4-dioxane; dichloromethane;

Reference yield:

: 42518-98-9
5-chlorothiophene-2-carbonyl chloride

: 1184298-47-2
5-chloro-thiophene-2-carboxylic acid [(S)-2-(3-bromo-2-methyl-benzenesulfonyl-amino)-3-(4-methyl-piperazin-1-yl)-3-oxo-propyl]-amide

Guidance literature:: Multi-step reaction with 4 steps

1: N-ethyl-N,N-diisopropylamine / dichloromethane / 20 °C

2: O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate; N-ethyl-N,N-diisopropylamine / dichloromethane / 16 h / 20 °C

3: hydrogenchloride / diethyl ether; ethyl acetate / 5 h / 20 °C

4: triethylamine / dichloromethane / 0 °C

With hydrogenchloride; O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate; triethylamine; N-ethyl-N,N-diisopropylamine; In diethyl ether; dichloromethane; ethyl acetate;