3-amino-6-chloro-7-(3-phenyl-1,2,4-oxadiazol-5-yl)-1,1-dioxo-1,4,2-benzodithiazine

Base Information

• Chemical Name: 3-amino-6-chloro-7-(3-phenyl-1,2,4-oxadiazol-5-yl)-1,1-dioxo-1,4,2-benzodithiazine
• CAS No.: 1398564-53-8
• Molecular Formula: C₁₅H₉ClN₄O₃S₂
• Molecular Weight: 392.846
• Mol file: 1398564-53-8.mol

Synonyms:3-amino-6-chloro-7-(3-phenyl-1,2,4-oxadiazol-5-yl)-1,1-dioxo-1,4,2-benzodithiazine

Chemical Property of 3-amino-6-chloro-7-(3-phenyl-1,2,4-oxadiazol-5-yl)-1,1-dioxo-1,4,2-benzodithiazine

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of 3-amino-6-chloro-7-(3-phenyl-1,2,4-oxadiazol-5-yl)-1,1-dioxo-1,4,2-benzodithiazine

There total 3 articles about 3-amino-6-chloro-7-(3-phenyl-1,2,4-oxadiazol-5-yl)-1,1-dioxo-1,4,2-benzodithiazine 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: 81.0%

6-chloro-3-methylthio-7-(3-phenyl-1,2,4-oxadiazol-5-yl)-1,1-dioxo-1,4,2-benzodithiazine (1398564-49-2) → 3-amino-6-chloro-7-(3-phenyl-1,2,4-oxadiazol-5-yl)-1,1-dioxo-1,4,2-benzodithiazine (1398564-53-8)

Guidance literature:

With ammonium hydroxide; In methanol; at 0 - 20 ℃;

DOI:10.1016/j.ejmech.2012.07.042

Reference yield:

6-chloro-3-(methylthio)-1,1-dioxo-1,4,2-benzodithiazine-7-carboxylic acid → 3-amino-6-chloro-7-(3-phenyl-1,2,4-oxadiazol-5-yl)-1,1-dioxo-1,4,2-benzodithiazine (1398564-53-8)

Guidance literature:

Multi-step reaction with 2 steps

1.1: thionyl chloride / benzene / 1 h / Reflux

1.2: 0 - 110 °C

2.1: ammonium hydroxide / methanol / 0 - 20 °C

With ammonium hydroxide; thionyl chloride; In methanol; benzene;

DOI:10.1016/j.ejmech.2012.07.042

Reference yield:

N-hydroxybenzenecarboximidamide (613-92-3) → 3-amino-6-chloro-7-(3-phenyl-1,2,4-oxadiazol-5-yl)-1,1-dioxo-1,4,2-benzodithiazine (1398564-53-8)

Guidance literature:

Multi-step reaction with 2 steps

1.1: thionyl chloride / benzene / 1 h / Reflux

1.2: 0 - 110 °C

2.1: ammonium hydroxide / methanol / 0 - 20 °C

With ammonium hydroxide; thionyl chloride; In methanol; benzene;

DOI:10.1016/j.ejmech.2012.07.042

upstream raw materials:

6-chloro-3-methylthio-7-(3-phenyl-1,2,4-oxadiazol-5-yl)-1,1-dioxo-1,4,2-benzodithiazine

N-hydroxybenzenecarboximidamide

Downstream raw materials:

C₂₃H₁₈ClN₅O₆S₂