2-(2,4-dichlorophenyl)-1-(4-(3-fluoropropoxy)phenyl)-5-methyl-1H-imidazole-4-carboxylic acid

Base Information

Chemical Name:2-(2,4-dichlorophenyl)-1-(4-(3-fluoropropoxy)phenyl)-5-methyl-1H-imidazole-4-carboxylic acid
CAS No.:930283-30-0
Molecular Formula:C₂₀H₁₇Cl₂FN₂O₃
Molecular Weight:423.271
Hs Code.:

Synonyms:2-(2,4-dichlorophenyl)-1-(4-(3-fluoropropoxy)phenyl)-5-methyl-1H-imidazole-4-carboxylic acid

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Chemical Property of 2-(2,4-dichlorophenyl)-1-(4-(3-fluoropropoxy)phenyl)-5-methyl-1H-imidazole-4-carboxylic acid

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Technology Process of 2-(2,4-dichlorophenyl)-1-(4-(3-fluoropropoxy)phenyl)-5-methyl-1H-imidazole-4-carboxylic acid

There total 6 articles about 2-(2,4-dichlorophenyl)-1-(4-(3-fluoropropoxy)phenyl)-5-methyl-1H-imidazole-4-carboxylic acid 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: 95.0%

: 930283-29-7
ethyl 2-(2,4-dichlorophenyl)-1-(4-(3-fluoropropoxy)phenyl)-5-methyl-1H-imidazole-4-carboxylate

: 930283-30-0
2-(2,4-dichlorophenyl)-1-(4-(3-fluoropropoxy)phenyl)-5-methyl-1H-imidazole-4-carboxylic acid

Guidance literature:: With water; potassium hydroxide; In tetrahydrofuran; ethanol; at 50 ℃; for 3.5h;
DOI:10.1021/acs.jmedchem.7b00861

Reference yield:

: 6574-98-7
2,4-dichlorobenzylnitrile

: 930283-30-0
2-(2,4-dichlorophenyl)-1-(4-(3-fluoropropoxy)phenyl)-5-methyl-1H-imidazole-4-carboxylic acid

Guidance literature:: Multi-step reaction with 6 steps

1.1: ethylmagnesium bromide / tetrahydrofuran / 0.33 h / Inert atmosphere

1.2: 20 h / 20 °C / Inert atmosphere

2.1: potassium carbonate / tetrahydrofuran / 0.17 h

2.2: 67 h / 20 °C

3.1: acetic acid; hydrogen bromide / 20 °C / Darkness

4.1: hydrogenchloride; magnesium sulfate / 1,4-dioxane / 2.5 h / Reflux

5.1: triphenylphosphine; diethylazodicarboxylate / tetrahydrofuran; toluene / 15 h / 20 °C

6.1: water; potassium hydroxide / tetrahydrofuran; ethanol / 3.5 h / 50 °C

With hydrogenchloride; ethylmagnesium bromide; water; hydrogen bromide; magnesium sulfate; potassium carbonate; acetic acid; triphenylphosphine; potassium hydroxide; diethylazodicarboxylate; In tetrahydrofuran; 1,4-dioxane; ethanol; toluene;
DOI:10.1021/acs.jmedchem.7b00861

Reference yield:

: 866598-55-2
N-(4-(benzyloxy)phenyl)-2,4-dichlorobenzamidine

: 930283-30-0
2-(2,4-dichlorophenyl)-1-(4-(3-fluoropropoxy)phenyl)-5-methyl-1H-imidazole-4-carboxylic acid

Guidance literature:: Multi-step reaction with 5 steps

1.1: potassium carbonate / tetrahydrofuran / 0.17 h

1.2: 67 h / 20 °C

2.1: acetic acid; hydrogen bromide / 20 °C / Darkness

3.1: hydrogenchloride; magnesium sulfate / 1,4-dioxane / 2.5 h / Reflux

4.1: triphenylphosphine; diethylazodicarboxylate / tetrahydrofuran; toluene / 15 h / 20 °C

5.1: water; potassium hydroxide / tetrahydrofuran; ethanol / 3.5 h / 50 °C

With hydrogenchloride; water; hydrogen bromide; magnesium sulfate; potassium carbonate; acetic acid; triphenylphosphine; potassium hydroxide; diethylazodicarboxylate; In tetrahydrofuran; 1,4-dioxane; ethanol; toluene;
DOI:10.1021/acs.jmedchem.7b00861