5-(4-fluorophenyl)-2-methanesulfonyl-1H-imidazole-4-carboxylic acid methyl ester

Base Information

Chemical Name:5-(4-fluorophenyl)-2-methanesulfonyl-1H-imidazole-4-carboxylic acid methyl ester
CAS No.:1422175-47-0
Molecular Formula:C₁₂H₁₁FN₂O₄S
Molecular Weight:298.295
Hs Code.:

Synonyms:5-(4-fluorophenyl)-2-methanesulfonyl-1H-imidazole-4-carboxylic acid methyl ester

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Chemical Property of 5-(4-fluorophenyl)-2-methanesulfonyl-1H-imidazole-4-carboxylic acid methyl ester

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Technology Process of 5-(4-fluorophenyl)-2-methanesulfonyl-1H-imidazole-4-carboxylic acid methyl ester

There total 5 articles about 5-(4-fluorophenyl)-2-methanesulfonyl-1H-imidazole-4-carboxylic acid methyl ester 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%

: 1422175-45-8
5-(4-fluorophenyl)-2-methylsulfanyl-1H-imidazole-4-carboxylic acid methyl ester

: 1422175-47-0
5-(4-fluorophenyl)-2-methanesulfonyl-1H-imidazole-4-carboxylic acid methyl ester

Guidance literature:: With potassium peroxymonosulfate; In methanol; water; at 20 ℃; for 5h;

Reference yield:

: 63131-29-3
methyl 4-fluorobenzoyl acetate

: 1422175-47-0
5-(4-fluorophenyl)-2-methanesulfonyl-1H-imidazole-4-carboxylic acid methyl ester

Guidance literature:: Multi-step reaction with 5 steps

1: sodium nitrite; acetic acid / water / 17 h / 10 - 20 °C

2: 5%-palladium/activated carbon; hydrogen; hydrogenchloride / water; methanol / 20 °C

3: N,N-dimethyl-formamide / 3 h / 95 °C

4: potassium carbonate / methanol / 2 h / 20 °C

5: potassium peroxymonosulfate / water; methanol / 5 h / 20 °C

With hydrogenchloride; potassium peroxymonosulfate; 5%-palladium/activated carbon; hydrogen; potassium carbonate; acetic acid; sodium nitrite; In methanol; water; N,N-dimethyl-formamide;

Reference yield:

: 93102-89-7
2-amino-3-(4-fluorophenyl)-3-oxo-propionic acid methyl ester hydrochloride

: 1422175-47-0
5-(4-fluorophenyl)-2-methanesulfonyl-1H-imidazole-4-carboxylic acid methyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: N,N-dimethyl-formamide / 3 h / 95 °C

2: potassium carbonate / methanol / 2 h / 20 °C

3: potassium peroxymonosulfate / water; methanol / 5 h / 20 °C

With potassium peroxymonosulfate; potassium carbonate; In methanol; water; N,N-dimethyl-formamide;