3-(2-[4-iodoacetamidophenyl]ethenyl)-6,7-dimethoxy-1-methyl-2(1H)-quinoxaline

Base Information

Chemical Name:3-(2-[4-iodoacetamidophenyl]ethenyl)-6,7-dimethoxy-1-methyl-2(1H)-quinoxaline
CAS No.:281674-36-0
Molecular Formula:C₂₁H₂₀IN₃O₄
Molecular Weight:505.312
Hs Code.:

Synonyms:3-(2-[4-iodoacetamidophenyl]ethenyl)-6,7-dimethoxy-1-methyl-2(1H)-quinoxaline

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Chemical Property of 3-(2-[4-iodoacetamidophenyl]ethenyl)-6,7-dimethoxy-1-methyl-2(1H)-quinoxaline

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Technology Process of 3-(2-[4-iodoacetamidophenyl]ethenyl)-6,7-dimethoxy-1-methyl-2(1H)-quinoxaline

There total 5 articles about 3-(2-[4-iodoacetamidophenyl]ethenyl)-6,7-dimethoxy-1-methyl-2(1H)-quinoxaline 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: 29.0%

: 281674-34-8
3-(2-[4-chloroacetamidophenyl]ethenyl)-6,7-dimethoxy-1-methyl-2(1H)-quinoxaline

: 281674-36-0
3-(2-[4-iodoacetamidophenyl]ethenyl)-6,7-dimethoxy-1-methyl-2(1H)-quinoxaline

Guidance literature:: With sodium iodide; In acetone; for 24h; Heating;

Reference yield:

: 122-85-0
para-acetamidobenzaldehyde

: 281674-36-0
3-(2-[4-iodoacetamidophenyl]ethenyl)-6,7-dimethoxy-1-methyl-2(1H)-quinoxaline

Guidance literature:: Multi-step reaction with 4 steps

1: 42 percent / piperidine; glacial AcOH / methanol / 24 h / Heating

2: 79 percent / aq. KOH / methanol / 24 h / Heating

3: 65 percent / N,N-diisopropylethylamine / dimethylformamide; tetrahydrofuran / -40 - 20 °C

4: 29 percent / NaI / acetone / 24 h / Heating

With piperidine; potassium hydroxide; acetic acid; N-ethyl-N,N-diisopropylamine; sodium iodide; In tetrahydrofuran; methanol; N,N-dimethyl-formamide; acetone; 1: Condensation / 2: Deacetylation / 3: Condensation / 4: Iodination;

Reference yield:

: 5761-60-4
6,7-dimethoxy-1,3-dimethyl-2(1H)-oxoquinoxaline

: 281674-36-0
3-(2-[4-iodoacetamidophenyl]ethenyl)-6,7-dimethoxy-1-methyl-2(1H)-quinoxaline

Guidance literature:: Multi-step reaction with 4 steps

1: 42 percent / piperidine; glacial AcOH / methanol / 24 h / Heating

2: 79 percent / aq. KOH / methanol / 24 h / Heating

3: 65 percent / N,N-diisopropylethylamine / dimethylformamide; tetrahydrofuran / -40 - 20 °C

4: 29 percent / NaI / acetone / 24 h / Heating

With piperidine; potassium hydroxide; acetic acid; N-ethyl-N,N-diisopropylamine; sodium iodide; In tetrahydrofuran; methanol; N,N-dimethyl-formamide; acetone; 1: Condensation / 2: Deacetylation / 3: Condensation / 4: Iodination;