methyl {4-[3-(2-chlorophenyl)-4-(4H-1,2,4-triazol-3-yl)-1H-pyrazol-1-yl]-5-methylpyridin-2-yl}carbamate

Base Information

Chemical Name:methyl {4-[3-(2-chlorophenyl)-4-(4H-1,2,4-triazol-3-yl)-1H-pyrazol-1-yl]-5-methylpyridin-2-yl}carbamate
CAS No.:1445888-95-8
Molecular Formula:C₁₉H₁₆ClN₇O₂
Molecular Weight:409.835
Hs Code.:

Synonyms:methyl {4-[3-(2-chlorophenyl)-4-(4H-1,2,4-triazol-3-yl)-1H-pyrazol-1-yl]-5-methylpyridin-2-yl}carbamate

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Chemical Property of methyl {4-[3-(2-chlorophenyl)-4-(4H-1,2,4-triazol-3-yl)-1H-pyrazol-1-yl]-5-methylpyridin-2-yl}carbamate

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Technology Process of methyl {4-[3-(2-chlorophenyl)-4-(4H-1,2,4-triazol-3-yl)-1H-pyrazol-1-yl]-5-methylpyridin-2-yl}carbamate

There total 4 articles about methyl {4-[3-(2-chlorophenyl)-4-(4H-1,2,4-triazol-3-yl)-1H-pyrazol-1-yl]-5-methylpyridin-2-yl}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: 41.0%

: 1445890-44-7
methyl {4-[3-(2-chlorophenyl)-4-(4-{[2-(trimethylsilyl)ethoxy]methyl}-4H-1,2,4-triazol-3-yl)-1H-pyrazol-1-yl]-5-methylpyridin-2-yl}carbamate

: 1445888-95-8
methyl {4-[3-(2-chlorophenyl)-4-(4H-1,2,4-triazol-3-yl)-1H-pyrazol-1-yl]-5-methylpyridin-2-yl}carbamate

Guidance literature:: With trifluoroacetic acid; In dichloromethane; at 20 ℃;

Reference yield:

: 1445888-28-7
N-{4-[3-(2-chlorophenyl)-4-(4H-1,2,4-triazol-3-yl)-1H-pyrazol-1-yl]-5-methylpyridin-2-yl}acetamide

: 1445888-95-8
methyl {4-[3-(2-chlorophenyl)-4-(4H-1,2,4-triazol-3-yl)-1H-pyrazol-1-yl]-5-methylpyridin-2-yl}carbamate

Guidance literature:: Multi-step reaction with 4 steps

1.1: sodium hydride / N,N-dimethyl-formamide; mineral oil / 0.08 h / 0 - 20 °C / Inert atmosphere

1.2: 24 h / 0 °C

2.1: sodium hydroxide; water / ethanol / 2 h / Reflux

3.1: triethylamine / dichloromethane / 6 h / 20 °C

4.1: trifluoroacetic acid / dichloromethane / 20 °C

With water; sodium hydride; triethylamine; trifluoroacetic acid; sodium hydroxide; In ethanol; dichloromethane; N,N-dimethyl-formamide; mineral oil;

Reference yield:

: 1445890-40-3
N-{4-[3-(2-chlorophenyl)-4-(4-{[2-(trimethylsilyl)ethoxy]methyl}-4H-1,2,4-triazol-3-yl)-1H-pyrazol-1-yl]-5-methylpyridin-2-yl}-N-{[2-(trimethylsilyl)ethoxy]methyl}acetamide

: 1445888-95-8
methyl {4-[3-(2-chlorophenyl)-4-(4H-1,2,4-triazol-3-yl)-1H-pyrazol-1-yl]-5-methylpyridin-2-yl}carbamate

Guidance literature:: Multi-step reaction with 3 steps

1: sodium hydroxide; water / ethanol / 2 h / Reflux

2: triethylamine / dichloromethane / 6 h / 20 °C

3: trifluoroacetic acid / dichloromethane / 20 °C

With water; triethylamine; trifluoroacetic acid; sodium hydroxide; In ethanol; dichloromethane;