7-(4-methoxybenzylthio)-2-methyl-4-nitrobenzo[d]thiazole

Base Information

• Chemical Name: 7-(4-methoxybenzylthio)-2-methyl-4-nitrobenzo[d]thiazole
• CAS No.: 1602770-00-2
• Molecular Formula: C₁₆H₁₄N₂O₃S₂
• Molecular Weight: 346.431
• Mol file: 1602770-00-2.mol

Synonyms:7-(4-methoxybenzylthio)-2-methyl-4-nitrobenzo[d]thiazole

Chemical Property of 7-(4-methoxybenzylthio)-2-methyl-4-nitrobenzo[d]thiazole

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of 7-(4-methoxybenzylthio)-2-methyl-4-nitrobenzo[d]thiazole

There total 4 articles about 7-(4-methoxybenzylthio)-2-methyl-4-nitrobenzo[d]thiazole 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: 75.0%

7-chloro-2-methyl-4-nitrobenzo[d]thiazole (1602769-99-2) + p-methoxybenzylmercaptan (6258-60-2) → 7-(4-methoxybenzylthio)-2-methyl-4-nitrobenzo[d]thiazole (1602770-00-2)

Guidance literature:

With potassium carbonate; In N,N-dimethyl-formamide; at 130 ℃; for 0.166667h; Microwave irradiation;

DOI:10.1002/cmdc.201300378

Reference yield:

3-chloro-2-fluoroaniline (2106-04-9) → 7-(4-methoxybenzylthio)-2-methyl-4-nitrobenzo[d]thiazole (1602770-00-2)

Guidance literature:

Multi-step reaction with 4 steps

1.1: 2 h / Reflux

2.1: Lawessons reagent / 5,5-dimethyl-1,3-cyclohexadiene / 2.5 h / 105 - 115 °C / Inert atmosphere

2.2: 16 h / Reflux; Inert atmosphere

3.1: sulfuric acid; potassium nitrate / 3 h / -10 - 20 °C / Inert atmosphere

4.1: potassium carbonate / N,N-dimethyl-formamide / 0.17 h / 130 °C / Microwave irradiation

With Lawessons reagent; sulfuric acid; potassium carbonate; potassium nitrate; In 5,5-dimethyl-1,3-cyclohexadiene; N,N-dimethyl-formamide;

DOI:10.1002/cmdc.201300378

Reference yield:

N-(3-chloro-2-fluorophenyl)acetamide (395-36-8) → 7-(4-methoxybenzylthio)-2-methyl-4-nitrobenzo[d]thiazole (1602770-00-2)

Guidance literature:

Multi-step reaction with 3 steps

1.1: Lawessons reagent / 5,5-dimethyl-1,3-cyclohexadiene / 2.5 h / 105 - 115 °C / Inert atmosphere

1.2: 16 h / Reflux; Inert atmosphere

2.1: sulfuric acid; potassium nitrate / 3 h / -10 - 20 °C / Inert atmosphere

3.1: potassium carbonate / N,N-dimethyl-formamide / 0.17 h / 130 °C / Microwave irradiation

With Lawessons reagent; sulfuric acid; potassium carbonate; potassium nitrate; In 5,5-dimethyl-1,3-cyclohexadiene; N,N-dimethyl-formamide;

DOI:10.1002/cmdc.201300378

upstream raw materials:

7-chloro-2-methyl-4-nitrobenzo[d]thiazole

p-methoxybenzylmercaptan

3-chloro-2-fluoroaniline

N-(3-chloro-2-fluorophenyl)acetamide