5-{5-amino-2-[4-(ethylsulfonyl)phenoxy]-4-iodophenyl}-1-methylpyrrolidin-2-one

Base Information

Chemical Name:5-{5-amino-2-[4-(ethylsulfonyl)phenoxy]-4-iodophenyl}-1-methylpyrrolidin-2-one
CAS No.:1616280-07-9
Molecular Formula:C₁₉H₂₁IN₂O₄S
Molecular Weight:500.357
Hs Code.:

Synonyms:5-{5-amino-2-[4-(ethylsulfonyl)phenoxy]-4-iodophenyl}-1-methylpyrrolidin-2-one

Suppliers and Price of 5-{5-amino-2-[4-(ethylsulfonyl)phenoxy]-4-iodophenyl}-1-methylpyrrolidin-2-one

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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 5-{5-amino-2-[4-(ethylsulfonyl)phenoxy]-4-iodophenyl}-1-methylpyrrolidin-2-one

Chemical Property:

Purity/Quality:: 99% ^*data from raw suppliers

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Technology Process of 5-{5-amino-2-[4-(ethylsulfonyl)phenoxy]-4-iodophenyl}-1-methylpyrrolidin-2-one

There total 13 articles about 5-{5-amino-2-[4-(ethylsulfonyl)phenoxy]-4-iodophenyl}-1-methylpyrrolidin-2-one 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: 92.0%

: 1616280-10-4
5-{5-amino-2-[4-(ethylsulfonyl)phenoxy]phenyl}-1-methylpyrrolidin-2-one

: 1616280-07-9
5-{5-amino-2-[4-(ethylsulfonyl)phenoxy]-4-iodophenyl}-1-methylpyrrolidin-2-one

Guidance literature:: With hydrogenchloride; potassium iodate; potassium iodide; In 1,4-dioxane; methanol; water; at 50 ℃; for 1.5h; Inert atmosphere;

Reference yield:

: 1616279-53-8
methyl 4-azido-4-(2-chloro-5-nitrophenyl)butanoate

: 1616280-07-9
5-{5-amino-2-[4-(ethylsulfonyl)phenoxy]-4-iodophenyl}-1-methylpyrrolidin-2-one

Guidance literature:: Multi-step reaction with 5 steps

1.1: triphenylphosphine / N,N-dimethyl-formamide / 2 h / 90 °C

1.2: 16 h / 90 °C

2.1: sodium hydride / tetrahydrofuran; N,N-dimethyl-formamide / 0.17 h / 0 °C

2.2: 1 h / 20 °C

3.1: potassium carbonate / N,N-dimethyl-formamide / 6 h / 120 °C

4.1: ammonium chloride; iron / methanol; tetrahydrofuran; water / 1 h / 100 °C

5.1: potassium iodide; potassium iodate; hydrogenchloride / methanol; water; 1,4-dioxane / 1.5 h / 50 °C / Inert atmosphere

With hydrogenchloride; potassium iodate; iron; sodium hydride; potassium carbonate; ammonium chloride; triphenylphosphine; potassium iodide; In tetrahydrofuran; 1,4-dioxane; methanol; water; N,N-dimethyl-formamide;

Reference yield:

: 1616281-06-1
methyl 4-(2-chloro-5-nitrophenyl)-4-hydroxybutanoate

: 1616280-07-9
5-{5-amino-2-[4-(ethylsulfonyl)phenoxy]-4-iodophenyl}-1-methylpyrrolidin-2-one

Guidance literature:: Multi-step reaction with 6 steps

1.1: diethylazodicarboxylate; diphenyl phosphoryl azide; triphenylphosphine / tetrahydrofuran / 0 - 20 °C

2.1: triphenylphosphine / N,N-dimethyl-formamide / 2 h / 90 °C

2.2: 16 h / 90 °C

3.1: sodium hydride / tetrahydrofuran; N,N-dimethyl-formamide / 0.17 h / 0 °C

3.2: 1 h / 20 °C

4.1: potassium carbonate / N,N-dimethyl-formamide / 6 h / 120 °C

5.1: ammonium chloride; iron / methanol; tetrahydrofuran; water / 1 h / 100 °C

6.1: potassium iodide; potassium iodate; hydrogenchloride / methanol; water; 1,4-dioxane / 1.5 h / 50 °C / Inert atmosphere

With hydrogenchloride; potassium iodate; diphenyl phosphoryl azide; iron; sodium hydride; potassium carbonate; ammonium chloride; triphenylphosphine; potassium iodide; diethylazodicarboxylate; In tetrahydrofuran; 1,4-dioxane; methanol; water; N,N-dimethyl-formamide;