5-hydroxy-2-(4-hydroxyphenyl)-3-methyl-1-<6-(4-nitroimidazol-1-yl)hexyl>indole

Base Information

Chemical Name:5-hydroxy-2-(4-hydroxyphenyl)-3-methyl-1-<6-(4-nitroimidazol-1-yl)hexyl>indole
CAS No.:130781-85-0
Molecular Formula:C₂₄H₂₆N₄O₄
Molecular Weight:434.495
Hs Code.:

Synonyms:5-hydroxy-2-(4-hydroxyphenyl)-3-methyl-1-<6-(4-nitroimidazol-1-yl)hexyl>indole

Suppliers and Price of 5-hydroxy-2-(4-hydroxyphenyl)-3-methyl-1-<6-(4-nitroimidazol-1-yl)hexyl>indole

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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-hydroxy-2-(4-hydroxyphenyl)-3-methyl-1-<6-(4-nitroimidazol-1-yl)hexyl>indole

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Technology Process of 5-hydroxy-2-(4-hydroxyphenyl)-3-methyl-1-<6-(4-nitroimidazol-1-yl)hexyl>indole

There total 5 articles about 5-hydroxy-2-(4-hydroxyphenyl)-3-methyl-1-<6-(4-nitroimidazol-1-yl)hexyl>indole 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: 75.0%

: 3034-38-6
1H-4⁽⁵⁾-nitroimidazole

: 130781-81-6
5-acetoxy-2-(4-acetoxyphenyl)-1-(6-bromohexyl)-3-methylindole

: 130781-85-0
5-hydroxy-2-(4-hydroxyphenyl)-3-methyl-1-<6-(4-nitroimidazol-1-yl)hexyl>indole

Guidance literature:: With sodium ethanolate; sodium iodide; In methanol; N,N-dimethyl-formamide; at 110 - 120 ℃; for 4h;
DOI:10.1002/ardp.19903230907

Reference yield:

: 629-03-8
1 ,6-dibromohexane

: 130781-85-0
5-hydroxy-2-(4-hydroxyphenyl)-3-methyl-1-<6-(4-nitroimidazol-1-yl)hexyl>indole

Guidance literature:: Multi-step reaction with 4 steps

1: 1.) NaH / 1.) DMF, 0 deg C, 45 min, 2.) room temperature, 4 h

2: BBr₃ / CH₂Cl₂ / 1.) 0 deg C, 30 min, 2.) room temp., 2 h

3: 1 h / Heating

4: 75 percent / EtONa, NaI / dimethylformamide; methanol / 4 h / 110 - 120 °C

With sodium ethanolate; boron tribromide; sodium hydride; sodium iodide; In methanol; dichloromethane; N,N-dimethyl-formamide;
DOI:10.1002/ardp.19903230907

Reference yield:

: 91444-18-7
5-methoxy-2-(4-methoxyphenyl)-3-methyl-1H-indole

: 130781-85-0
5-hydroxy-2-(4-hydroxyphenyl)-3-methyl-1-<6-(4-nitroimidazol-1-yl)hexyl>indole

Guidance literature:: Multi-step reaction with 4 steps

1: 1.) NaH / 1.) DMF, 0 deg C, 45 min, 2.) room temperature, 4 h

2: BBr₃ / CH₂Cl₂ / 1.) 0 deg C, 30 min, 2.) room temp., 2 h

3: 1 h / Heating

4: 75 percent / EtONa, NaI / dimethylformamide; methanol / 4 h / 110 - 120 °C

With sodium ethanolate; boron tribromide; sodium hydride; sodium iodide; In methanol; dichloromethane; N,N-dimethyl-formamide;
DOI:10.1002/ardp.19903230907