2-(2-chlorophenyl)-3-[4-(methylsulfanyl) phenyl]-5-nitroimidazo[2,1-b][1,3] benzothiazole

Base Information

Chemical Name:2-(2-chlorophenyl)-3-[4-(methylsulfanyl) phenyl]-5-nitroimidazo[2,1-b][1,3] benzothiazole
CAS No.:1370024-00-2
Molecular Formula:C₂₂H₁₄ClN₃O₂S₂
Molecular Weight:451.957
Hs Code.:

Synonyms:2-(2-chlorophenyl)-3-[4-(methylsulfanyl) phenyl]-5-nitroimidazo[2,1-b][1,3] benzothiazole

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Chemical Property of 2-(2-chlorophenyl)-3-[4-(methylsulfanyl) phenyl]-5-nitroimidazo[2,1-b][1,3] benzothiazole

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Technology Process of 2-(2-chlorophenyl)-3-[4-(methylsulfanyl) phenyl]-5-nitroimidazo[2,1-b][1,3] benzothiazole

There total 6 articles about 2-(2-chlorophenyl)-3-[4-(methylsulfanyl) phenyl]-5-nitroimidazo[2,1-b][1,3] benzothiazole 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: 85.14%

: 6973-51-9
2-amino-4-nitrobenzothiazole

: 1280582-80-0
C₁₅H₁₂BrClOS

: 1370024-00-2
2-(2-chlorophenyl)-3-[4-(methylsulfanyl) phenyl]-5-nitroimidazo[2,1-b][1,3] benzothiazole

Guidance literature:: In ethanol; Reflux;

Reference yield:

: 2444-36-2
2'-chloro-benzeneacetic acid

: 1370024-00-2
2-(2-chlorophenyl)-3-[4-(methylsulfanyl) phenyl]-5-nitroimidazo[2,1-b][1,3] benzothiazole

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;

Reference yield:

: 955016-68-9
C₁₅H₁₃ClOS

: 1370024-00-2
2-(2-chlorophenyl)-3-[4-(methylsulfanyl) phenyl]-5-nitroimidazo[2,1-b][1,3] benzothiazole

Guidance literature:: Multi-step reaction with 2 steps

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

2: ethanol / Reflux

With bromine; In ethanol; chloroform;