2-[4-({(E)-[ethyl(methyl)amino]methylidene}amino)-2,5-dimethylbenzyl]-4-(4-methylphenyl)-1,3-thiazole-5-carboxamide

Base Information

Chemical Name:2-[4-({(E)-[ethyl(methyl)amino]methylidene}amino)-2,5-dimethylbenzyl]-4-(4-methylphenyl)-1,3-thiazole-5-carboxamide
CAS No.:1421921-06-3
Molecular Formula:C₂₄H₂₈N₄OS
Molecular Weight:420.579
Hs Code.:

Synonyms:2-[4-({(E)-[ethyl(methyl)amino]methylidene}amino)-2,5-dimethylbenzyl]-4-(4-methylphenyl)-1,3-thiazole-5-carboxamide

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Chemical Property of 2-[4-({(E)-[ethyl(methyl)amino]methylidene}amino)-2,5-dimethylbenzyl]-4-(4-methylphenyl)-1,3-thiazole-5-carboxamide

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Technology Process of 2-[4-({(E)-[ethyl(methyl)amino]methylidene}amino)-2,5-dimethylbenzyl]-4-(4-methylphenyl)-1,3-thiazole-5-carboxamide

There total 8 articles about 2-[4-({(E)-[ethyl(methyl)amino]methylidene}amino)-2,5-dimethylbenzyl]-4-(4-methylphenyl)-1,3-thiazole-5-carboxamide 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:

: 28860-25-5
N-methyl-N-ethylformamide

: 1421922-26-0
2-(4-amino-2,5-dimethylbenzyl)-4-(4-methylphenyl)-1,3-thiazole-5-carboxamide

: 1421921-06-3
2-[4-({(E)-[ethyl(methyl)amino]methylidene}amino)-2,5-dimethylbenzyl]-4-(4-methylphenyl)-1,3-thiazole-5-carboxamide

Guidance literature:: N-methyl-N-ethylformamide; With oxalyl dichloride; In chloroform; at 20 ℃; for 0.166667h; Inert atmosphere;

2-(4-amino-2,5-dimethylbenzyl)-4-(4-methylphenyl)-1,3-thiazole-5-carboxamide; In chloroform; at 20 ℃; for 1h; Inert atmosphere;

Reference yield:

: 1421922-22-6
2-(2,5-dimethyl-4-nitrobenzyl)-4-(4-methylphenyl)-1,3-thiazole-5-carboxylic acid

: 1421921-06-3
2-[4-({(E)-[ethyl(methyl)amino]methylidene}amino)-2,5-dimethylbenzyl]-4-(4-methylphenyl)-1,3-thiazole-5-carboxamide

Guidance literature:: Multi-step reaction with 3 steps

1.1: ammonium chloride; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; benzotriazol-1-ol; triethylamine / N,N-dimethyl-formamide / 24 h / 20 °C

2.1: ammonium chloride; iron; water / ethanol / 2 h / Reflux

3.1: oxalyl dichloride / chloroform / 0.17 h / 20 °C / Inert atmosphere

3.2: 1 h / 20 °C / Inert atmosphere

With oxalyl dichloride; water; iron; ammonium chloride; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; In ethanol; chloroform; N,N-dimethyl-formamide;

Reference yield:

: 16213-85-7
(2,5-dimethylphenyl)acetonitrile

: 1421921-06-3
2-[4-({(E)-[ethyl(methyl)amino]methylidene}amino)-2,5-dimethylbenzyl]-4-(4-methylphenyl)-1,3-thiazole-5-carboxamide

Guidance literature:: Multi-step reaction with 7 steps

1.1: nitric acid / 0.5 h / Cooling with ice

2.1: hydrogenchloride; O,O-Diethyl hydrogen phosphorodithioate / ethyl acetate / 24 h / 20 °C

3.1: isopropyl alcohol / 2 h / 80 °C

4.1: sodium hydroxide; water / methanol / 4 h / 20 °C

5.1: ammonium chloride; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; benzotriazol-1-ol; triethylamine / N,N-dimethyl-formamide / 24 h / 20 °C

6.1: ammonium chloride; iron; water / ethanol / 2 h / Reflux

7.1: oxalyl dichloride / chloroform / 0.17 h / 20 °C / Inert atmosphere

7.2: 1 h / 20 °C / Inert atmosphere

With hydrogenchloride; oxalyl dichloride; water; nitric acid; iron; ammonium chloride; benzotriazol-1-ol; O,O-Diethyl hydrogen phosphorodithioate; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; sodium hydroxide; In methanol; ethanol; chloroform; ethyl acetate; N,N-dimethyl-formamide; isopropyl alcohol;