N-(3-chloro-4-methylphenyl)-2-hydrazino-N-methyl-4-phenylthiazole-5-carboxamide

Base Information

Chemical Name:N-(3-chloro-4-methylphenyl)-2-hydrazino-N-methyl-4-phenylthiazole-5-carboxamide
CAS No.:1429312-20-8
Molecular Formula:C₁₈H₁₇ClN₄OS
Molecular Weight:372.878
Hs Code.:

Synonyms:N-(3-chloro-4-methylphenyl)-2-hydrazino-N-methyl-4-phenylthiazole-5-carboxamide

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Chemical Property of N-(3-chloro-4-methylphenyl)-2-hydrazino-N-methyl-4-phenylthiazole-5-carboxamide

Chemical Property:

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Technology Process of N-(3-chloro-4-methylphenyl)-2-hydrazino-N-methyl-4-phenylthiazole-5-carboxamide

There total 6 articles about N-(3-chloro-4-methylphenyl)-2-hydrazino-N-methyl-4-phenylthiazole-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: 80.0%

di-tert-butyl 2-(5-((3-chloro-4-methylphenyl)(methyl)carbamoyl)-4-phenylthiazol-2-yl)hydrazine-1,1-dicarboxylate: 1429312-18-4
di-tert-butyl 2-(5-((3-chloro-4-methylphenyl)(methyl)carbamoyl)-4-phenylthiazol-2-yl)hydrazine-1,1-dicarboxylate

N-(3-chloro-4-methylphenyl)-2-hydrazino-N-methyl-4-phenylthiazole-5-carboxamide: 1429312-20-8
N-(3-chloro-4-methylphenyl)-2-hydrazino-N-methyl-4-phenylthiazole-5-carboxamide

Guidance literature:: With hydrogenchloride; In 1,4-dioxane; at 20 ℃;

Reference yield:

: 1429312-19-5
2-[2,2-bis(tert-butoxycarbonyl)hydrazino]-4-phenylthiazole-5-carboxylic acid

N-(3-chloro-4-methylphenyl)-2-hydrazino-N-methyl-4-phenylthiazole-5-carboxamide: 1429312-20-8
N-(3-chloro-4-methylphenyl)-2-hydrazino-N-methyl-4-phenylthiazole-5-carboxamide

Guidance literature:: Multi-step reaction with 2 steps

1: 2-chloro-1-methyl-pyridinium iodide; triethylamine / dichloromethane / 3 h / 20 °C

2: hydrogenchloride / 1,4-dioxane / 20 °C

With hydrogenchloride; 2-chloro-1-methyl-pyridinium iodide; triethylamine; In 1,4-dioxane; dichloromethane;

Reference yield:

: 1429312-16-2
tert-butyl N-[(4-phenylthiazol-2-yl)amino]carbamate

N-(3-chloro-4-methylphenyl)-2-hydrazino-N-methyl-4-phenylthiazole-5-carboxamide: 1429312-20-8
N-(3-chloro-4-methylphenyl)-2-hydrazino-N-methyl-4-phenylthiazole-5-carboxamide

Guidance literature:: Multi-step reaction with 5 steps

1.1: triethylamine; dmap / tetrahydrofuran / 1 h / 0 - 20 °C

2.1: diisopropylamine; n-butyllithium / tetrahydrofuran; hexane / 1 h / -78 °C / Inert atmosphere

2.2: 1 h / -78 °C

3.1: lithium hydroxide / tetrahydrofuran / 48 h / 20 °C

4.1: 2-chloro-1-methyl-pyridinium iodide; triethylamine / dichloromethane / 3 h / 20 °C

5.1: hydrogenchloride / 1,4-dioxane / 20 °C

With hydrogenchloride; dmap; n-butyllithium; 2-chloro-1-methyl-pyridinium iodide; triethylamine; diisopropylamine; lithium hydroxide; In tetrahydrofuran; 1,4-dioxane; hexane; dichloromethane;