2-amino-N-methyl-N-[1-(3-chlorophenyl)-3-methyl-1H-pyrazol-5-yl]benzamide

Base Information

Chemical Name:2-amino-N-methyl-N-[1-(3-chlorophenyl)-3-methyl-1H-pyrazol-5-yl]benzamide
CAS No.:1394810-00-4
Molecular Formula:C₁₈H₁₇ClN₄O
Molecular Weight:340.812
Hs Code.:

Synonyms:2-amino-N-methyl-N-[1-(3-chlorophenyl)-3-methyl-1H-pyrazol-5-yl]benzamide

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Chemical Property of 2-amino-N-methyl-N-[1-(3-chlorophenyl)-3-methyl-1H-pyrazol-5-yl]benzamide

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Technology Process of 2-amino-N-methyl-N-[1-(3-chlorophenyl)-3-methyl-1H-pyrazol-5-yl]benzamide

There total 4 articles about 2-amino-N-methyl-N-[1-(3-chlorophenyl)-3-methyl-1H-pyrazol-5-yl]benzamide 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: 82.0%

: 1394809-94-9
N-methyl-N-[3-methyl-1-(3-chlorophenyl)-1H-pyrazol-5-yl]-2-nitrobenzamide

: 1394810-00-4
2-amino-N-methyl-N-[1-(3-chlorophenyl)-3-methyl-1H-pyrazol-5-yl]benzamide

Guidance literature:: With iron; acetic acid; In water; at 100 ℃; for 1.75h;
DOI:10.1016/j.ejmech.2012.06.028

Reference yield:

: 1394809-88-1
C₁₃H₁₄ClN₃O

: 1394810-00-4
2-amino-N-methyl-N-[1-(3-chlorophenyl)-3-methyl-1H-pyrazol-5-yl]benzamide

Guidance literature:: Multi-step reaction with 3 steps

1.1: potassium hydroxide / ethanol; water / 10 h / Reflux

2.1: chloroform / 1 h / Reflux

2.2: 4 h / Reflux

3.1: iron; acetic acid / water / 1.75 h / 100 °C

With iron; acetic acid; potassium hydroxide; In ethanol; chloroform; water;
DOI:10.1016/j.ejmech.2012.06.028

Reference yield:

: 105438-65-1
5-Acetamido-1-(3-chlorophenyl)-3-methylpyrazole

: 1394810-00-4
2-amino-N-methyl-N-[1-(3-chlorophenyl)-3-methyl-1H-pyrazol-5-yl]benzamide

Guidance literature:: Multi-step reaction with 4 steps

1.1: ethanol; sodium hydride / 10 h / 20 °C

2.1: potassium hydroxide / ethanol; water / 10 h / Reflux

3.1: chloroform / 1 h / Reflux

3.2: 4 h / Reflux

4.1: iron; acetic acid / water / 1.75 h / 100 °C

With ethanol; iron; sodium hydride; acetic acid; potassium hydroxide; In ethanol; chloroform; water;
DOI:10.1016/j.ejmech.2012.06.028