(6-chloro-7-methyl-1,1-dioxo-1H-1λ⁶-benzo[1,4,2]dithiazin-3-yl)-(3,4-dichloro-phenyl)-methanone

Base Information

• Chemical Name: (6-chloro-7-methyl-1,1-dioxo-1H-1λ⁶-benzo[1,4,2]dithiazin-3-yl)-(3,4-dichloro-phenyl)-methanone
• CAS No.: 732301-64-3
• Molecular Formula: C₁₅H₈Cl₃NO₃S₂
• Molecular Weight: 420.724
• Mol file: 732301-64-3.mol

Synonyms:(6-chloro-7-methyl-1,1-dioxo-1H-1λ⁶-benzo[1,4,2]dithiazin-3-yl)-(3,4-dichloro-phenyl)-methanone

Chemical Property of (6-chloro-7-methyl-1,1-dioxo-1H-1λ⁶-benzo[1,4,2]dithiazin-3-yl)-(3,4-dichloro-phenyl)-methanone

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of (6-chloro-7-methyl-1,1-dioxo-1H-1λ⁶-benzo[1,4,2]dithiazin-3-yl)-(3,4-dichloro-phenyl)-methanone

There total 3 articles about (6-chloro-7-methyl-1,1-dioxo-1H-1λ⁶-benzo[1,4,2]dithiazin-3-yl)-(3,4-dichloro-phenyl)-methanone 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: 45.0%

4-chloro-2-{[2-(3,4-dichlorophenyl)-2-oxoethyl]sulfanyl}-5-methylbenzenesulfonamide → (6-chloro-7-methyl-1,1-dioxo-1H-1λ6-benzo[1,4,2]dithiazin-3-yl)-(3,4-dichloro-phenyl)-methanone (732301-64-3)

Guidance literature:

With thionyl chloride; for 46h; Heating;

DOI:10.1016/j.bmc.2004.04.024

Reference yield:

2-bromo-1-(3,4-dichlorophenyl)ethanone (2632-10-2) → (6-chloro-7-methyl-1,1-dioxo-1H-1λ6-benzo[1,4,2]dithiazin-3-yl)-(3,4-dichloro-phenyl)-methanone (732301-64-3)

Guidance literature:

Multi-step reaction with 2 steps

1: 66 percent / Et₃N / CH₂Cl₂ / 6 h / Heating

2: 45 percent / thionyl chloride / 46 h / Heating

With thionyl chloride; triethylamine; In dichloromethane;

DOI:10.1016/j.bmc.2004.04.024

Reference yield:

4-chloro-2-mercapto-5-methyl-benzenesulfonamide (95792-62-4) → (6-chloro-7-methyl-1,1-dioxo-1H-1λ6-benzo[1,4,2]dithiazin-3-yl)-(3,4-dichloro-phenyl)-methanone (732301-64-3)

Guidance literature:

Multi-step reaction with 2 steps

1: 66 percent / Et₃N / CH₂Cl₂ / 6 h / Heating

2: 45 percent / thionyl chloride / 46 h / Heating

With thionyl chloride; triethylamine; In dichloromethane;

DOI:10.1016/j.bmc.2004.04.024

upstream raw materials:

2-bromo-1-(3,4-dichlorophenyl)ethanone

4-chloro-2-mercapto-5-methyl-benzenesulfonamide

Downstream raw materials:

6-chloro-3-(3,4-dichlorobenzoyl)-7-methyl-2,3-dihydro-1,1-dioxo-1,4,2-benzodithiazine