N-[5-(4-(3-chloro-2-(4-chlorophenyl)-4-oxoazetidin-1-yl)-5-mercapto-4H-1,2,4-triazol-3-yl)-4-methylthiazol-2-yl]acetamide

Base Information

Chemical Name:N-[5-(4-(3-chloro-2-(4-chlorophenyl)-4-oxoazetidin-1-yl)-5-mercapto-4H-1,2,4-triazol-3-yl)-4-methylthiazol-2-yl]acetamide
CAS No.:1315460-44-6
Molecular Formula:C₁₇H₁₄Cl₂N₆O₂S₂
Molecular Weight:469.375
Hs Code.:

Synonyms:N-[5-(4-(3-chloro-2-(4-chlorophenyl)-4-oxoazetidin-1-yl)-5-mercapto-4H-1,2,4-triazol-3-yl)-4-methylthiazol-2-yl]acetamide

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Chemical Property of N-[5-(4-(3-chloro-2-(4-chlorophenyl)-4-oxoazetidin-1-yl)-5-mercapto-4H-1,2,4-triazol-3-yl)-4-methylthiazol-2-yl]acetamide

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Technology Process of N-[5-(4-(3-chloro-2-(4-chlorophenyl)-4-oxoazetidin-1-yl)-5-mercapto-4H-1,2,4-triazol-3-yl)-4-methylthiazol-2-yl]acetamide

There total 6 articles about N-[5-(4-(3-chloro-2-(4-chlorophenyl)-4-oxoazetidin-1-yl)-5-mercapto-4H-1,2,4-triazol-3-yl)-4-methylthiazol-2-yl]acetamide 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: 65.0%

: 1315460-36-6
C₁₅H₁₃ClN₆OS₂

: 79-04-9
chloroacetyl chloride

: 1315460-44-6
N-[5-(4-(3-chloro-2-(4-chlorophenyl)-4-oxoazetidin-1-yl)-5-mercapto-4H-1,2,4-triazol-3-yl)-4-methylthiazol-2-yl]acetamide

Guidance literature:: With triethylamine; In 1,4-dioxane; at 0 - 20 ℃; Reflux;

Reference yield:

: 1315460-33-3
potassium dithiocarbazinate

: 1315460-44-6
N-[5-(4-(3-chloro-2-(4-chlorophenyl)-4-oxoazetidin-1-yl)-5-mercapto-4H-1,2,4-triazol-3-yl)-4-methylthiazol-2-yl]acetamide

Guidance literature:: Multi-step reaction with 3 steps

1: hydrazine hydrate / ethanol / Reflux

2: acetic acid / ethanol / 2 h / Reflux

3: triethylamine / 1,4-dioxane / 0 - 20 °C / Reflux

With hydrazine hydrate; acetic acid; triethylamine; In 1,4-dioxane; ethanol;

Reference yield:

: 7210-76-6
ethyl-2-amino-4-methylthiazole-5-carboxylate

: 1315460-44-6
N-[5-(4-(3-chloro-2-(4-chlorophenyl)-4-oxoazetidin-1-yl)-5-mercapto-4H-1,2,4-triazol-3-yl)-4-methylthiazol-2-yl]acetamide

Guidance literature:: Multi-step reaction with 6 steps

1: 1 h / Reflux

2: hydrazine hydrate / ethanol / 6.17 h / Reflux

3: potassium hydroxide / ethanol / 20 °C / Cooling with ice

4: hydrazine hydrate / ethanol / Reflux

5: acetic acid / ethanol / 2 h / Reflux

6: triethylamine / 1,4-dioxane / 0 - 20 °C / Reflux

With hydrazine hydrate; acetic acid; triethylamine; potassium hydroxide; In 1,4-dioxane; ethanol;