(1-methyl-1H-imidazol-5-yl)(3-phenyl-2,4-bis(trifluoromethyl)quinolin-6-yl)(pyridin-2-yl)methanol

Base Information

Chemical Name:(1-methyl-1H-imidazol-5-yl)(3-phenyl-2,4-bis(trifluoromethyl)quinolin-6-yl)(pyridin-2-yl)methanol
CAS No.:1600566-89-9
Molecular Formula:C₂₇H₁₈F₆N₄O
Molecular Weight:528.457
Hs Code.:

Synonyms:(1-methyl-1H-imidazol-5-yl)(3-phenyl-2,4-bis(trifluoromethyl)quinolin-6-yl)(pyridin-2-yl)methanol

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Chemical Property of (1-methyl-1H-imidazol-5-yl)(3-phenyl-2,4-bis(trifluoromethyl)quinolin-6-yl)(pyridin-2-yl)methanol

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Technology Process of (1-methyl-1H-imidazol-5-yl)(3-phenyl-2,4-bis(trifluoromethyl)quinolin-6-yl)(pyridin-2-yl)methanol

There total 5 articles about (1-methyl-1H-imidazol-5-yl)(3-phenyl-2,4-bis(trifluoromethyl)quinolin-6-yl)(pyridin-2-yl)methanol 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:

: 1600562-93-3
6-iodo-3-phenyl-2,4-bis(trifluoromethyl)quinoline

: 1599529-17-5
(1-methyl-1H-imidazol-5-yl)(pyridin-2-yl)methanone

: 1600566-89-9
(1-methyl-1H-imidazol-5-yl)(3-phenyl-2,4-bis(trifluoromethyl)quinolin-6-yl)(pyridin-2-yl)methanol

Guidance literature:: 6-iodo-3-phenyl-2,4-bis(trifluoromethyl)quinoline; With n-butyllithium; In tetrahydrofuran; hexane; for 0.0333333h; Cooling with acetone-dry ice;

(1-methyl-1H-imidazol-5-yl)(pyridin-2-yl)methanone; In tetrahydrofuran; hexane; for 0.166667h; Cooling with acetone-dry ice;

With water; In tetrahydrofuran; methanol; hexane;

Reference yield:

: 460-00-4
1-Bromo-4-fluorobenzene

: 1600566-89-9
(1-methyl-1H-imidazol-5-yl)(3-phenyl-2,4-bis(trifluoromethyl)quinolin-6-yl)(pyridin-2-yl)methanol

Guidance literature:: Multi-step reaction with 5 steps

1.1: diisopropylamine; n-butyllithium / tetrahydrofuran; hexane / 0.1 h / -68 °C / Inert atmosphere; Cooling with acetone-dry ice

1.2: Inert atmosphere

2.1: sodium azide / dimethyl sulfoxide / 1 h / 95 °C

2.2: 0.5 h / 20 °C

3.1: tributyl-amine / N,N-dimethyl-formamide / 2 h / 130 °C

4.1: copper(l) iodide; N,N`-dimethylethylenediamine; sodium iodide / tert-butyl alcohol / 0.5 h / 150 °C / Microwave irradiation

5.1: n-butyllithium / tetrahydrofuran; hexane / 0.03 h / Cooling with acetone-dry ice

5.2: 0.17 h / Cooling with acetone-dry ice

With copper(l) iodide; n-butyllithium; sodium azide; tributyl-amine; diisopropylamine; sodium iodide; N,N`-dimethylethylenediamine; In tetrahydrofuran; hexane; dimethyl sulfoxide; N,N-dimethyl-formamide; tert-butyl alcohol;

Reference yield:

: 617706-15-7
1-(5-bromo-2-fluorophenyl)-2,2,2-trifluoro-ethanone

: 1600566-89-9
(1-methyl-1H-imidazol-5-yl)(3-phenyl-2,4-bis(trifluoromethyl)quinolin-6-yl)(pyridin-2-yl)methanol

Guidance literature:: Multi-step reaction with 4 steps

1.1: sodium azide / dimethyl sulfoxide / 1 h / 95 °C

1.2: 0.5 h / 20 °C

2.1: tributyl-amine / N,N-dimethyl-formamide / 2 h / 130 °C

3.1: copper(l) iodide; N,N`-dimethylethylenediamine; sodium iodide / tert-butyl alcohol / 0.5 h / 150 °C / Microwave irradiation

4.1: n-butyllithium / tetrahydrofuran; hexane / 0.03 h / Cooling with acetone-dry ice

4.2: 0.17 h / Cooling with acetone-dry ice

With copper(l) iodide; n-butyllithium; sodium azide; tributyl-amine; sodium iodide; N,N`-dimethylethylenediamine; In tetrahydrofuran; hexane; dimethyl sulfoxide; N,N-dimethyl-formamide; tert-butyl alcohol;