3-cyclohexyl-2-(4-fluorophenyl)-1-methyl-1H-imidazo[1,2-b]pyrazole-7-carboxylic acid

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Chemical Name:3-cyclohexyl-2-(4-fluorophenyl)-1-methyl-1H-imidazo[1,2-b]pyrazole-7-carboxylic acid
CAS No.:1427549-95-8
Molecular Formula:C₁₉H₂₀FN₃O₂
Molecular Weight:341.385
Hs Code.:

Synonyms:3-cyclohexyl-2-(4-fluorophenyl)-1-methyl-1H-imidazo[1,2-b]pyrazole-7-carboxylic acid

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Chemical Property of 3-cyclohexyl-2-(4-fluorophenyl)-1-methyl-1H-imidazo[1,2-b]pyrazole-7-carboxylic acid

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Technology Process of 3-cyclohexyl-2-(4-fluorophenyl)-1-methyl-1H-imidazo[1,2-b]pyrazole-7-carboxylic acid

There total 7 articles about 3-cyclohexyl-2-(4-fluorophenyl)-1-methyl-1H-imidazo[1,2-b]pyrazole-7-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:

: 1427549-93-6
ethyl 3-cyclohexyl-2-(4-fluorophenyl)-1-methyl-imidazo[1,2-b]pyrazole-7-carboxylate

: 1427549-95-8
3-cyclohexyl-2-(4-fluorophenyl)-1-methyl-1H-imidazo[1,2-b]pyrazole-7-carboxylic acid

: 1427549-97-0
3-cyclohexyl-2-(4-fluorophenyl)-1-methyl-1H-imidazo[1,2-b]pyrazole

Guidance literature:: With water; lithium hydroxide; In tetrahydrofuran; methanol; at 60 ℃; for 6h;

Reference yield:

: 403-42-9
1-(4-fluorophenyl)ethanone

: 1427549-95-8
3-cyclohexyl-2-(4-fluorophenyl)-1-methyl-1H-imidazo[1,2-b]pyrazole-7-carboxylic acid

: 1427549-97-0
3-cyclohexyl-2-(4-fluorophenyl)-1-methyl-1H-imidazo[1,2-b]pyrazole

Guidance literature:: Multi-step reaction with 6 steps

1.1: lithium hexamethyldisilazane / tetrahydrofuran / 0.5 h / -78 °C

1.2: 0.5 h / -78 °C

2.1: triethylsilane; trifluoroacetic acid / dichloromethane / 16 h / 20 °C

3.1: bromine / 1,4-dioxane; diethyl ether / 2 h / 20 °C

4.1: potassium carbonate / N,N-dimethyl-formamide / 4 h / 20 °C

4.2: 2 h / 65 °C

5.1: potassium carbonate / N,N-dimethyl-formamide / 16 h

6.1: water; lithium hydroxide / tetrahydrofuran; methanol / 6 h / 60 °C

With triethylsilane; water; bromine; potassium carbonate; trifluoroacetic acid; lithium hydroxide; lithium hexamethyldisilazane; In tetrahydrofuran; 1,4-dioxane; methanol; diethyl ether; dichloromethane; N,N-dimethyl-formamide;

Reference yield:

: 71666-48-3
2-cyclohexyl-1-(4-fluorophenyl)ethanone

: 1427549-95-8
3-cyclohexyl-2-(4-fluorophenyl)-1-methyl-1H-imidazo[1,2-b]pyrazole-7-carboxylic acid

: 1427549-97-0
3-cyclohexyl-2-(4-fluorophenyl)-1-methyl-1H-imidazo[1,2-b]pyrazole

Guidance literature:: Multi-step reaction with 4 steps

1.1: bromine / 1,4-dioxane; diethyl ether / 2 h / 20 °C

2.1: potassium carbonate / N,N-dimethyl-formamide / 4 h / 20 °C

2.2: 2 h / 65 °C

3.1: potassium carbonate / N,N-dimethyl-formamide / 16 h

4.1: water; lithium hydroxide / tetrahydrofuran; methanol / 6 h / 60 °C

With water; bromine; potassium carbonate; lithium hydroxide; In tetrahydrofuran; 1,4-dioxane; methanol; diethyl ether; N,N-dimethyl-formamide;