2-(2,4-dichlorophenyl)-3-[4-(methylsulfanyl)phenyl]imidazo[2,1-b][1,3]benzothiazole-7-carboxylic acid

Base Information

Chemical Name:2-(2,4-dichlorophenyl)-3-[4-(methylsulfanyl)phenyl]imidazo[2,1-b][1,3]benzothiazole-7-carboxylic acid
CAS No.:1370023-99-6
Molecular Formula:C₂₃H₁₄Cl₂N₂O₂S₂
Molecular Weight:485.414
Hs Code.:

Synonyms:2-(2,4-dichlorophenyl)-3-[4-(methylsulfanyl)phenyl]imidazo[2,1-b][1,3]benzothiazole-7-carboxylic acid

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Chemical Property of 2-(2,4-dichlorophenyl)-3-[4-(methylsulfanyl)phenyl]imidazo[2,1-b][1,3]benzothiazole-7-carboxylic acid

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Technology Process of 2-(2,4-dichlorophenyl)-3-[4-(methylsulfanyl)phenyl]imidazo[2,1-b][1,3]benzothiazole-7-carboxylic acid

There total 6 articles about 2-(2,4-dichlorophenyl)-3-[4-(methylsulfanyl)phenyl]imidazo[2,1-b][1,3]benzothiazole-7-carboxylic acid 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: 85.67%

: 93-85-6
2-aminobenzothiazole-6-carboxylic acid

: 1280582-87-7
C₁₅H₁₁BrCl₂OS

: 1370023-99-6
2-(2,4-dichlorophenyl)-3-[4-(methylsulfanyl)phenyl]imidazo[2,1-b][1,3]benzothiazole-7-carboxylic acid

Guidance literature:: In ethanol; Reflux;

Reference yield:

: 1280582-78-6
C₁₅H₁₂Cl₂OS

: 1370023-99-6
2-(2,4-dichlorophenyl)-3-[4-(methylsulfanyl)phenyl]imidazo[2,1-b][1,3]benzothiazole-7-carboxylic acid

Guidance literature:: Multi-step reaction with 2 steps

1: bromine / chloroform / 0.5 h / 50 °C

2: ethanol / Reflux

With bromine; In ethanol; chloroform;

Reference yield:

: 100-68-5
methyl-phenyl-thioether

: 1370023-99-6
2-(2,4-dichlorophenyl)-3-[4-(methylsulfanyl)phenyl]imidazo[2,1-b][1,3]benzothiazole-7-carboxylic acid

Guidance literature:: Multi-step reaction with 3 steps

1: phosphoric acid; trifluoroacetic anhydride / 0.5 h / 25 °C

2: bromine / chloroform / 0.5 h / 50 °C

3: ethanol / Reflux

With phosphoric acid; bromine; trifluoroacetic anhydride; In ethanol; chloroform;