N-(4-acetyl-5-(2-chloroquinolin-3-yl)-4,5-dihydro-1,3,4-thiadiazol-2-yl)-N-(4-nitrophenyl)acetamide

Base Information

• Chemical Name: N-(4-acetyl-5-(2-chloroquinolin-3-yl)-4,5-dihydro-1,3,4-thiadiazol-2-yl)-N-(4-nitrophenyl)acetamide
• CAS No.: 1313028-04-4
• Molecular Formula: C₂₁H₁₆ClN₅O₄S
• Molecular Weight: 469.908
• Mol file: 1313028-04-4.mol

Synonyms:N-(4-acetyl-5-(2-chloroquinolin-3-yl)-4,5-dihydro-1,3,4-thiadiazol-2-yl)-N-(4-nitrophenyl)acetamide

Chemical Property of N-(4-acetyl-5-(2-chloroquinolin-3-yl)-4,5-dihydro-1,3,4-thiadiazol-2-yl)-N-(4-nitrophenyl)acetamide

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of N-(4-acetyl-5-(2-chloroquinolin-3-yl)-4,5-dihydro-1,3,4-thiadiazol-2-yl)-N-(4-nitrophenyl)acetamide

There total 4 articles about N-(4-acetyl-5-(2-chloroquinolin-3-yl)-4,5-dihydro-1,3,4-thiadiazol-2-yl)-N-(4-nitrophenyl)acetamide 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: 65.0%

1-((2-chloroquinolin-3-yl)methylene)-4-p-nitrophenylthiosemicarbazide (1313027-74-5) + acetic anhydride (108-24-7) → N-(4-acetyl-5-(2-chloroquinolin-3-yl)-4,5-dihydro-1,3,4-thiadiazol-2-yl)-N-(4-nitrophenyl)acetamide (1313028-04-4)

Guidance literature:

Reflux;

DOI:10.1016/j.ejmech.2011.04.013

Reference yield:

-essigsaeure (13037-51-9) → N-(4-acetyl-5-(2-chloroquinolin-3-yl)-4,5-dihydro-1,3,4-thiadiazol-2-yl)-N-(4-nitrophenyl)acetamide (1313028-04-4)

Guidance literature:

Multi-step reaction with 3 steps

1.1: hydrazine hydrate

2.1: ethanol

2.2: 12 h / 60 °C

3.1: Reflux

With hydrazine hydrate; In ethanol;

DOI:10.1016/j.ejmech.2011.04.013

Reference yield:

4-nitro-aniline (100-01-6,104810-17-5) → N-(4-acetyl-5-(2-chloroquinolin-3-yl)-4,5-dihydro-1,3,4-thiadiazol-2-yl)-N-(4-nitrophenyl)acetamide (1313028-04-4)

Guidance literature:

Multi-step reaction with 4 steps

1.1: potassium hydroxide / water

2.1: hydrazine hydrate

3.1: ethanol

3.2: 12 h / 60 °C

4.1: Reflux

With hydrazine hydrate; potassium hydroxide; In ethanol; water;

DOI:10.1016/j.ejmech.2011.04.013

upstream raw materials:

1-((2-chloroquinolin-3-yl)methylene)-4-p-nitrophenylthiosemicarbazide

acetic anhydride

2-chloro-3-quinoline carboxaldehyde

4-(4-nitrophenyl)-3-thiosemicarbazide