methyl 2-chloro-5-{[5-(4-fluorophenyl)-2-trifluoromethyl-3H-imidazole-4-carbonyl]amino}benzoate

Base Information

Chemical Name:methyl 2-chloro-5-{[5-(4-fluorophenyl)-2-trifluoromethyl-3H-imidazole-4-carbonyl]amino}benzoate
CAS No.:1422175-55-0
Molecular Formula:C₁₉H₁₂ClF₄N₃O₃
Molecular Weight:441.769
Hs Code.:

Synonyms:methyl 2-chloro-5-{[5-(4-fluorophenyl)-2-trifluoromethyl-3H-imidazole-4-carbonyl]amino}benzoate

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Chemical Property of methyl 2-chloro-5-{[5-(4-fluorophenyl)-2-trifluoromethyl-3H-imidazole-4-carbonyl]amino}benzoate

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Technology Process of methyl 2-chloro-5-{[5-(4-fluorophenyl)-2-trifluoromethyl-3H-imidazole-4-carbonyl]amino}benzoate

There total 6 articles about methyl 2-chloro-5-{[5-(4-fluorophenyl)-2-trifluoromethyl-3H-imidazole-4-carbonyl]amino}benzoate 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: 33.0%

: 1208114-38-8
5-(4-fluorophenyl)-2-(trifluoromethyl)-1H-imidazole-4-carboxylic acid

: 42122-75-8
methyl 2-chloro-5-aminobenzoate

: 1422175-55-0
methyl 2-chloro-5-{[5-(4-fluorophenyl)-2-trifluoromethyl-3H-imidazole-4-carbonyl]amino}benzoate

Guidance literature:: 5-(4-fluorophenyl)-2-(trifluoromethyl)-1H-imidazole-4-carboxylic acid; With N-ethyl-N,N-diisopropylamine; HATU; In dichloromethane; for 0.25h;

methyl 2-chloro-5-aminobenzoate; In dichloromethane; for 48h; Reflux;

Reference yield:

: 7292-73-1
(2RS)-N-(p-fluorophenyl)glycine

: 1422175-55-0
methyl 2-chloro-5-{[5-(4-fluorophenyl)-2-trifluoromethyl-3H-imidazole-4-carbonyl]amino}benzoate

Guidance literature:: Multi-step reaction with 4 steps

1.1: 2 h / 20 °C

2.1: tributylphosphine / toluene / 12 h / 20 °C

3.1: 5%-palladium/activated carbon; hydrogen / ethanol / 2585.81 Torr

4.1: HATU; N-ethyl-N,N-diisopropylamine / dichloromethane / 0.25 h

4.2: 48 h / Reflux

With tributylphosphine; 5%-palladium/activated carbon; hydrogen; N-ethyl-N,N-diisopropylamine; HATU; In ethanol; dichloromethane; toluene;

Reference yield:

: 6307-82-0
2-chloro-5-nitro-benzoic acid methyl ester

: 1422175-55-0
methyl 2-chloro-5-{[5-(4-fluorophenyl)-2-trifluoromethyl-3H-imidazole-4-carbonyl]amino}benzoate

Guidance literature:: Multi-step reaction with 2 steps

1.1: tin(II) chloride dihdyrate; ethanol / 2 h / Sealed tube; Sonication

2.1: HATU; N-ethyl-N,N-diisopropylamine / dichloromethane / 0.25 h

2.2: 48 h / Reflux

With tin(II) chloride dihdyrate; ethanol; N-ethyl-N,N-diisopropylamine; HATU; In dichloromethane;