(2,4-dichloro-8-methyl-3-phenylquinolin-6-yl)(1-methyl-1H-imidazol-5-yl)methanol

Base Information

Chemical Name:(2,4-dichloro-8-methyl-3-phenylquinolin-6-yl)(1-methyl-1H-imidazol-5-yl)methanol
CAS No.:1600563-22-1
Molecular Formula:C₂₁H₁₇Cl₂N₃O
Molecular Weight:398.291
Hs Code.:

Synonyms:(2,4-dichloro-8-methyl-3-phenylquinolin-6-yl)(1-methyl-1H-imidazol-5-yl)methanol

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Chemical Property of (2,4-dichloro-8-methyl-3-phenylquinolin-6-yl)(1-methyl-1H-imidazol-5-yl)methanol

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Technology Process of (2,4-dichloro-8-methyl-3-phenylquinolin-6-yl)(1-methyl-1H-imidazol-5-yl)methanol

There total 4 articles about (2,4-dichloro-8-methyl-3-phenylquinolin-6-yl)(1-methyl-1H-imidazol-5-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:

: 1003-21-0
5-bromo-N-methylimidazole

: 1600563-20-9
2,4-dichloro-8-methyl-3-phenylquinoline-6-carbaldehyde

: 1600563-22-1
(2,4-dichloro-8-methyl-3-phenylquinolin-6-yl)(1-methyl-1H-imidazol-5-yl)methanol

Guidance literature:: 5-bromo-N-methylimidazole; With TurboGrignard; In tetrahydrofuran; dichloromethane; at 20 ℃; for 0.166667h; Cooling with ice; Inert atmosphere;

2,4-dichloro-8-methyl-3-phenylquinoline-6-carbaldehyde; With lanthanium (III) chloride bis(lithium chloride) complex; In tetrahydrofuran; dichloromethane; at 20 ℃; for 0.75h; Inert atmosphere; Cooling with ice;

Reference yield:

: 2613-89-0
phenylmalonic acid

: 1600563-22-1
(2,4-dichloro-8-methyl-3-phenylquinolin-6-yl)(1-methyl-1H-imidazol-5-yl)methanol

Guidance literature:: Multi-step reaction with 4 steps

1.1: trichlorophosphate / 0.17 h / 130 °C

2.1: 2 h / Reflux

3.1: n-butyllithium / tetrahydrofuran; hexane; N,N-dimethyl-formamide / 0.5 h / -72 - -71 °C / Inert atmosphere

4.1: TurboGrignard / dichloromethane; tetrahydrofuran / 0.17 h / 20 °C / Cooling with ice; Inert atmosphere

4.2: 0.75 h / 20 °C / Inert atmosphere; Cooling with ice

With TurboGrignard; n-butyllithium; trichlorophosphate; In tetrahydrofuran; hexane; dichloromethane; N,N-dimethyl-formamide;

Reference yield:

: 1600563-19-6
6-bromo-2,4-dichloro-8-methyl-3-phenylquinoline

: 1600563-22-1
(2,4-dichloro-8-methyl-3-phenylquinolin-6-yl)(1-methyl-1H-imidazol-5-yl)methanol

Guidance literature:: Multi-step reaction with 2 steps

1.1: n-butyllithium / tetrahydrofuran; hexane; N,N-dimethyl-formamide / 0.5 h / -72 - -71 °C / Inert atmosphere

2.1: TurboGrignard / dichloromethane; tetrahydrofuran / 0.17 h / 20 °C / Cooling with ice; Inert atmosphere

2.2: 0.75 h / 20 °C / Inert atmosphere; Cooling with ice

With TurboGrignard; n-butyllithium; In tetrahydrofuran; hexane; dichloromethane; N,N-dimethyl-formamide;