4-(3-chloro-phenyl)-2-(6-oxiranylmethoxy-benzoimidazol-1-yl)-thiazole-5-carboxylic acid amide

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Chemical Name:4-(3-chloro-phenyl)-2-(6-oxiranylmethoxy-benzoimidazol-1-yl)-thiazole-5-carboxylic acid amide
CAS No.:1232234-88-6
Molecular Formula:C₂₀H₁₅ClN₄O₃S
Molecular Weight:426.883
Hs Code.:

Synonyms:4-(3-chloro-phenyl)-2-(6-oxiranylmethoxy-benzoimidazol-1-yl)-thiazole-5-carboxylic acid amide

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Chemical Property of 4-(3-chloro-phenyl)-2-(6-oxiranylmethoxy-benzoimidazol-1-yl)-thiazole-5-carboxylic acid amide

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Technology Process of 4-(3-chloro-phenyl)-2-(6-oxiranylmethoxy-benzoimidazol-1-yl)-thiazole-5-carboxylic acid amide

There total 7 articles about 4-(3-chloro-phenyl)-2-(6-oxiranylmethoxy-benzoimidazol-1-yl)-thiazole-5-carboxylic acid amide 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:

: 1232234-83-1
2-(6-benzyloxy-benzoimidazol-1-yl)-4-(3-chloro-phenyl)-thiazole-5-carboxylic acid amide

: 1232234-88-6
4-(3-chloro-phenyl)-2-(6-oxiranylmethoxy-benzoimidazol-1-yl)-thiazole-5-carboxylic acid amide

Guidance literature:: Multi-step reaction with 2 steps

1: boron dimethyl-trifluoro sulphide / dichloromethane / 0 - 20 °C

2: potassium carbonate / potassium iodide / N,N-dimethyl-formamide / 3 h / 100 °C

With boron dimethyl-trifluoro sulphide; potassium carbonate; potassium iodide; In dichloromethane; N,N-dimethyl-formamide;

Reference yield:

: 1232234-80-8
2-(2-amino-5-benzyloxy-phenylamino)-4-(3-chloro-phenyl)-thiazole-5-carboxylic acid ethyl ester

: 1232234-88-6
4-(3-chloro-phenyl)-2-(6-oxiranylmethoxy-benzoimidazol-1-yl)-thiazole-5-carboxylic acid amide

Guidance literature:: Multi-step reaction with 5 steps

1.1: acetic acid / 1 h / 50 °C

2.1: water; lithium hydroxide / tetrahydrofuran / 3 h / 60 °C

2.2: pH ~ 3 - 4

3.1: ammonium chloride; N-ethyl-N,N-diisopropylamine; N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate / N,N-dimethyl-formamide / 1 h / 20 °C

4.1: boron dimethyl-trifluoro sulphide / dichloromethane / 0 - 20 °C

5.1: potassium carbonate / potassium iodide / N,N-dimethyl-formamide / 3 h / 100 °C

With boron dimethyl-trifluoro sulphide; water; potassium carbonate; ammonium chloride; acetic acid; N-ethyl-N,N-diisopropylamine; N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate; lithium hydroxide; potassium iodide; In tetrahydrofuran; dichloromethane; N,N-dimethyl-formamide;

Reference yield:

: 1232234-82-0
2-(6-benzyloxy-benzoimidazol-1-yl)-4-(3-chloro-phenyl)-thiazole-5-carboxylic acid

: 1232234-88-6
4-(3-chloro-phenyl)-2-(6-oxiranylmethoxy-benzoimidazol-1-yl)-thiazole-5-carboxylic acid amide

Guidance literature:: Multi-step reaction with 3 steps

1: ammonium chloride; N-ethyl-N,N-diisopropylamine; N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate / N,N-dimethyl-formamide / 1 h / 20 °C

2: boron dimethyl-trifluoro sulphide / dichloromethane / 0 - 20 °C

3: potassium carbonate / potassium iodide / N,N-dimethyl-formamide / 3 h / 100 °C

With boron dimethyl-trifluoro sulphide; potassium carbonate; ammonium chloride; N-ethyl-N,N-diisopropylamine; N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate; potassium iodide; In dichloromethane; N,N-dimethyl-formamide;