methyl N-[[2-chloro-5-[1-(4-methylphenyl)methyl-1H-1,2,3-triazol-4-yl]phenyl]methyl]carbamate

Base Information

Chemical Name:methyl N-[[2-chloro-5-[1-(4-methylphenyl)methyl-1H-1,2,3-triazol-4-yl]phenyl]methyl]carbamate
CAS No.:1067197-12-9
Molecular Formula:C₁₉H₁₉ClN₄O₂
Molecular Weight:370.838
Hs Code.:

Synonyms:methyl N-[[2-chloro-5-[1-(4-methylphenyl)methyl-1H-1,2,3-triazol-4-yl]phenyl]methyl]carbamate

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Chemical Property of methyl N-[[2-chloro-5-[1-(4-methylphenyl)methyl-1H-1,2,3-triazol-4-yl]phenyl]methyl]carbamate

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Technology Process of methyl N-[[2-chloro-5-[1-(4-methylphenyl)methyl-1H-1,2,3-triazol-4-yl]phenyl]methyl]carbamate

There total 6 articles about methyl N-[[2-chloro-5-[1-(4-methylphenyl)methyl-1H-1,2,3-triazol-4-yl]phenyl]methyl]carbamate 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:

: 1067197-08-3
methyl N-[[2-chloro-5-(1H-1,2,3-triazol-5-yl)phenyl]methyl]carbamate

: 104-81-4
4-Methylbenzyl bromide

: 1067197-12-9
methyl N-[[2-chloro-5-[1-(4-methylphenyl)methyl-1H-1,2,3-triazol-4-yl]phenyl]methyl]carbamate

: 1067197-09-4
methyl N-[[2-chloro-5-[2-(4-methylphenyl)methyl-2H-1,2,3-triazol-4-yl]phenyl]methyl]carbamate

Guidance literature:: With potassium carbonate; In N,N-dimethyl-formamide; at 100 ℃; for 24h;

Reference yield:

: 116632-41-8
1-chloro-4-iodo-2-methylbenzene

: 1067197-12-9
methyl N-[[2-chloro-5-[1-(4-methylphenyl)methyl-1H-1,2,3-triazol-4-yl]phenyl]methyl]carbamate

: 1067197-09-4
methyl N-[[2-chloro-5-[2-(4-methylphenyl)methyl-2H-1,2,3-triazol-4-yl]phenyl]methyl]carbamate

Guidance literature:: Multi-step reaction with 6 steps

1: 2,2'-azobis(isobutyronitrile); N-Bromosuccinimide / dichloromethane; water / 2 h / Irradiation

2: potassium carbonate / 1 h / 110 °C

3: triethylamine; triphenylphosphine; copper(l) iodide / bis-triphenylphosphine-palladium(II) chloride / tetrahydrofuran / 0.5 h / 20 °C

4: potassium hydroxide / methanol / 18 h / 20 °C

5: trimethylsilylazide; copper(l) iodide / N,N-dimethyl-formamide; methanol / 8 h / 100 °C / Microwave irradiation

6: potassium carbonate / N,N-dimethyl-formamide / 24 h / 100 °C

With N-Bromosuccinimide; copper(l) iodide; 2,2'-azobis(isobutyronitrile); trimethylsilylazide; potassium carbonate; triethylamine; triphenylphosphine; potassium hydroxide; bis-triphenylphosphine-palladium(II) chloride; In tetrahydrofuran; methanol; dichloromethane; water; N,N-dimethyl-formamide;

Reference yield:

: 1067197-20-9
methyl [(2-chloro-5-iodophenyl)methyl]carbamate

: 1067197-12-9
methyl N-[[2-chloro-5-[1-(4-methylphenyl)methyl-1H-1,2,3-triazol-4-yl]phenyl]methyl]carbamate

: 1067197-09-4
methyl N-[[2-chloro-5-[2-(4-methylphenyl)methyl-2H-1,2,3-triazol-4-yl]phenyl]methyl]carbamate

Guidance literature:: Multi-step reaction with 4 steps

1: triethylamine; triphenylphosphine; copper(l) iodide / bis-triphenylphosphine-palladium(II) chloride / tetrahydrofuran / 0.5 h / 20 °C

2: potassium hydroxide / methanol / 18 h / 20 °C

3: trimethylsilylazide; copper(l) iodide / N,N-dimethyl-formamide; methanol / 8 h / 100 °C / Microwave irradiation

4: potassium carbonate / N,N-dimethyl-formamide / 24 h / 100 °C

With copper(l) iodide; trimethylsilylazide; potassium carbonate; triethylamine; triphenylphosphine; potassium hydroxide; bis-triphenylphosphine-palladium(II) chloride; In tetrahydrofuran; methanol; N,N-dimethyl-formamide;