(R)-2-oxoimidazolidine-4-carboxylic acid {1-(4-fluorophenyl)-5-[3-fluoro-5-((R)-2,2,2-trifluoro-1-methylethoxymethyl)phenyl]-1H-pyrazol-3-yl}amide

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Chemical Name:(R)-2-oxoimidazolidine-4-carboxylic acid {1-(4-fluorophenyl)-5-[3-fluoro-5-((R)-2,2,2-trifluoro-1-methylethoxymethyl)phenyl]-1H-pyrazol-3-yl}amide
CAS No.:1426404-47-8
Molecular Formula:C₂₃H₂₀F₅N₅O₃
Molecular Weight:509.436
Hs Code.:

Synonyms:(R)-2-oxoimidazolidine-4-carboxylic acid {1-(4-fluorophenyl)-5-[3-fluoro-5-((R)-2,2,2-trifluoro-1-methylethoxymethyl)phenyl]-1H-pyrazol-3-yl}amide

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Chemical Property of (R)-2-oxoimidazolidine-4-carboxylic acid {1-(4-fluorophenyl)-5-[3-fluoro-5-((R)-2,2,2-trifluoro-1-methylethoxymethyl)phenyl]-1H-pyrazol-3-yl}amide

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Technology Process of (R)-2-oxoimidazolidine-4-carboxylic acid {1-(4-fluorophenyl)-5-[3-fluoro-5-((R)-2,2,2-trifluoro-1-methylethoxymethyl)phenyl]-1H-pyrazol-3-yl}amide

There total 6 articles about (R)-2-oxoimidazolidine-4-carboxylic acid {1-(4-fluorophenyl)-5-[3-fluoro-5-((R)-2,2,2-trifluoro-1-methylethoxymethyl)phenyl]-1H-pyrazol-3-yl}amide 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:

: 1426408-84-5
1-(4-fluorophenyl)-5-[3-fluoro-5-((R)-2,2,2-trifluoro-1-methylethoxymethyl)phenyl]-1H-pyrazol-3-ylamine

: 214767-15-4
(R)-2-oxoimidazolidine-4-carboxylic acid

: 1426404-47-8
(R)-2-oxoimidazolidine-4-carboxylic acid {1-(4-fluorophenyl)-5-[3-fluoro-5-((R)-2,2,2-trifluoro-1-methylethoxymethyl)phenyl]-1H-pyrazol-3-yl}amide

Guidance literature:: With 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In chloroform; at 20 ℃; for 3h;

Reference yield:

: 1426408-79-8
3-(2,5-dimethylpyrrol-1-yl)-1-(4-fluorophenyl)-1H-pyrazole

: 1426404-47-8
(R)-2-oxoimidazolidine-4-carboxylic acid {1-(4-fluorophenyl)-5-[3-fluoro-5-((R)-2,2,2-trifluoro-1-methylethoxymethyl)phenyl]-1H-pyrazol-3-yl}amide

Guidance literature:: Multi-step reaction with 2 steps

1: tricyclohexylphosphine; palladium diacetate; potassium carbonate / water; 1,4-dioxane / 2 h / 105 °C

2: 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / chloroform / 3 h / 20 °C

With palladium diacetate; potassium carbonate; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; tricyclohexylphosphine; In 1,4-dioxane; chloroform; water; 1: |Suzuki Coupling;

Reference yield:

: 456-41-7
1-(Bromomethyl)-3-fluorobenzene

: 1426404-47-8
(R)-2-oxoimidazolidine-4-carboxylic acid {1-(4-fluorophenyl)-5-[3-fluoro-5-((R)-2,2,2-trifluoro-1-methylethoxymethyl)phenyl]-1H-pyrazol-3-yl}amide

Guidance literature:: Multi-step reaction with 4 steps

1.1: sodium hydride / N,N-dimethyl-formamide; mineral oil / 0.42 h / 0 °C / Inert atmosphere

1.2: 2 h / Inert atmosphere

2.1: 4,4'-di-tert-butyl-2,2'-bipyridine; (1,5-cyclooctadiene)(methoxy)iridium(I) dimer / tetrahydrofuran / 16 h / Inert atmosphere; Reflux

3.1: tricyclohexylphosphine; palladium diacetate; potassium carbonate / water; 1,4-dioxane / 2 h / 105 °C

4.1: 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / chloroform / 3 h / 20 °C

With (1,5-cyclooctadiene)(methoxy)iridium(I) dimer; palladium diacetate; sodium hydride; potassium carbonate; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; 4,4'-di-tert-butyl-2,2'-bipyridine; tricyclohexylphosphine; In tetrahydrofuran; 1,4-dioxane; chloroform; water; N,N-dimethyl-formamide; mineral oil; 2.1: |Suzuki Coupling / 3.1: |Suzuki Coupling;