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

Base Information

Chemical Name:(4-chlorophenyl)(1-methyl-1H-imidazol-5-yl)(3-phenyl-2,4-bis(trifluoromethyl)quinolin-6-yl)methanol
CAS No.:1600565-83-0
Molecular Formula:C₂₈H₁₈ClF₆N₃O
Molecular Weight:561.914
Hs Code.:

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

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

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

There total 7 articles about (4-chlorophenyl)(1-methyl-1H-imidazol-5-yl)(3-phenyl-2,4-bis(trifluoromethyl)quinolin-6-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:

: (4-chlorophenyl)(1-methyl-1H-imidazol-5-yl)-methanone

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

: 1600565-83-0
(4-chlorophenyl)(1-methyl-1H-imidazol-5-yl)(3-phenyl-2,4-bis(trifluoromethyl)quinolin-6-yl)methanol

Guidance literature:: 6-iodo-3-phenyl-2,4-bis(trifluoromethyl)quinoline; With isopropylmagnesium chloride; In tetrahydrofuran; at -78 ℃; for 0.333333h; Inert atmosphere;

(4-chlorophenyl)(1-methyl-1H-imidazol-5-yl)-methanone; In tetrahydrofuran; at 20 ℃; Inert atmosphere;

With water; ammonium chloride; In tetrahydrofuran; Inert atmosphere;

Reference yield:

: 122-01-0
4-chloro-benzoyl chloride

: 1600565-83-0
(4-chlorophenyl)(1-methyl-1H-imidazol-5-yl)(3-phenyl-2,4-bis(trifluoromethyl)quinolin-6-yl)methanol

Guidance literature:: Multi-step reaction with 3 steps

1.1: pyridine / dichloromethane / 72 h / 20 °C

2.1: ethylmagnesium bromide / tetrahydrofuran; diethyl ether / 0.33 h / Inert atmosphere; Cooling with ice

2.2: 20 °C / Inert atmosphere

3.1: isopropylmagnesium chloride / tetrahydrofuran / 0.33 h / -78 °C / Inert atmosphere

3.2: 20 °C / Inert atmosphere

3.3: Inert atmosphere

With pyridine; ethylmagnesium bromide; isopropylmagnesium chloride; In tetrahydrofuran; diethyl ether; dichloromethane;

Reference yield:

: 122334-37-6
4-chloro-N-methoxy-N-methylbenzamide

: 1600565-83-0
(4-chlorophenyl)(1-methyl-1H-imidazol-5-yl)(3-phenyl-2,4-bis(trifluoromethyl)quinolin-6-yl)methanol

Guidance literature:: Multi-step reaction with 2 steps

1.1: ethylmagnesium bromide / tetrahydrofuran; diethyl ether / 0.33 h / Inert atmosphere; Cooling with ice

1.2: 20 °C / Inert atmosphere

2.1: isopropylmagnesium chloride / tetrahydrofuran / 0.33 h / -78 °C / Inert atmosphere

2.2: 20 °C / Inert atmosphere

2.3: Inert atmosphere

With ethylmagnesium bromide; isopropylmagnesium chloride; In tetrahydrofuran; diethyl ether;