5-[3-chloro-5-((R)-2,2,2-trifluoro-1-methylethoxymethyl)phenyl]-1-(4-fluorophenyl)-1H-pyrazol-3-ylamine

Base Information

Chemical Name:5-[3-chloro-5-((R)-2,2,2-trifluoro-1-methylethoxymethyl)phenyl]-1-(4-fluorophenyl)-1H-pyrazol-3-ylamine
CAS No.:1426408-88-9
Molecular Formula:C₁₉H₁₆ClF₄N₃O
Molecular Weight:413.802
Hs Code.:

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

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Chemical Property of 5-[3-chloro-5-((R)-2,2,2-trifluoro-1-methylethoxymethyl)phenyl]-1-(4-fluorophenyl)-1H-pyrazol-3-ylamine

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Technology Process of 5-[3-chloro-5-((R)-2,2,2-trifluoro-1-methylethoxymethyl)phenyl]-1-(4-fluorophenyl)-1H-pyrazol-3-ylamine

There total 5 articles about 5-[3-chloro-5-((R)-2,2,2-trifluoro-1-methylethoxymethyl)phenyl]-1-(4-fluorophenyl)-1H-pyrazol-3-ylamine 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:

: 1426408-81-2
1-(4-fluorophenyl)-5-iodo-1H-pyrazol-3-ylamine

: 1426408-86-7
2-[3-chloro-5-((R)-2,2,2-trifluoro-1-methylethoxymethyl)phenyl]-4,4,5,5-tetramethyl[1,3,2]dioxaborolane

: 1426408-88-9
5-[3-chloro-5-((R)-2,2,2-trifluoro-1-methylethoxymethyl)phenyl]-1-(4-fluorophenyl)-1H-pyrazol-3-ylamine

Guidance literature:: With palladium diacetate; sodium carbonate; tricyclohexylphosphine; In 1,2-dimethoxyethane; water; at 100 ℃; for 2h;

Reference yield:

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

: 1426408-88-9
5-[3-chloro-5-((R)-2,2,2-trifluoro-1-methylethoxymethyl)phenyl]-1-(4-fluorophenyl)-1H-pyrazol-3-ylamine

Guidance literature:: Multi-step reaction with 3 steps

1.1: n-butyllithium / tetrahydrofuran; hexane / 0.5 h / -78 °C / Inert atmosphere

1.2: 0.5 h / Inert atmosphere

2.1: hydroxylamine hydrochloride; triethylamine / water; ethanol / 15 h / 95 °C

3.1: sodium carbonate; tricyclohexylphosphine; palladium diacetate / water; 1,2-dimethoxyethane / 2 h / 100 °C

With n-butyllithium; hydroxylamine hydrochloride; palladium diacetate; sodium carbonate; triethylamine; tricyclohexylphosphine; In tetrahydrofuran; 1,2-dimethoxyethane; ethanol; hexane; water; 3.1: |Suzuki Coupling;

Reference yield:

: 1426408-85-6
1-chloro-3-((R)-2,2,2-trifluoro-1-methylethoxymethyl)benzene

: 1426408-88-9
5-[3-chloro-5-((R)-2,2,2-trifluoro-1-methylethoxymethyl)phenyl]-1-(4-fluorophenyl)-1H-pyrazol-3-ylamine

Guidance literature:: Multi-step reaction with 2 steps

1: 4,4'-di-tert-butyl-2,2'-bipyridine; (1,5-cyclooctadiene)(methoxy)iridium(I) dimer / tetrahydrofuran / 13 h / Inert atmosphere; Reflux

2: sodium carbonate; tricyclohexylphosphine; palladium diacetate / water; 1,2-dimethoxyethane / 2 h / 100 °C

With (1,5-cyclooctadiene)(methoxy)iridium(I) dimer; palladium diacetate; sodium carbonate; 4,4'-di-tert-butyl-2,2'-bipyridine; tricyclohexylphosphine; In tetrahydrofuran; 1,2-dimethoxyethane; water; 1: |Suzuki Coupling / 2: |Suzuki Coupling;