3-(2-chloro-3,3,3-trifluoroprop-1-enyl)-2,2-dimethyl-N-[5-(3,4,5-trimethoxyphenyl)-1,3,4-thiadiazol-2-yl]cyclopropanecarboxamide

Base Information

• Chemical Name: 3-(2-chloro-3,3,3-trifluoroprop-1-enyl)-2,2-dimethyl-N-[5-(3,4,5-trimethoxyphenyl)-1,3,4-thiadiazol-2-yl]cyclopropanecarboxamide
• CAS No.: 1019855-22-1
• Molecular Formula: C₂₀H₂₁ClF₃N₃O₄S
• Molecular Weight: 491.919
• Mol file: 1019855-22-1.mol

Synonyms:3-(2-chloro-3,3,3-trifluoroprop-1-enyl)-2,2-dimethyl-N-[5-(3,4,5-trimethoxyphenyl)-1,3,4-thiadiazol-2-yl]cyclopropanecarboxamide

Chemical Property of 3-(2-chloro-3,3,3-trifluoroprop-1-enyl)-2,2-dimethyl-N-[5-(3,4,5-trimethoxyphenyl)-1,3,4-thiadiazol-2-yl]cyclopropanecarboxamide

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of 3-(2-chloro-3,3,3-trifluoroprop-1-enyl)-2,2-dimethyl-N-[5-(3,4,5-trimethoxyphenyl)-1,3,4-thiadiazol-2-yl]cyclopropanecarboxamide

There total 2 articles about 3-(2-chloro-3,3,3-trifluoroprop-1-enyl)-2,2-dimethyl-N-[5-(3,4,5-trimethoxyphenyl)-1,3,4-thiadiazol-2-yl]cyclopropanecarboxamide 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: 72.8%

2-(3,4,5-trimethoxyphenyl)-5-amino-1,3,4-thiadiazole (28004-59-3) + 3-(2-chloro-3,3,3-trifluoroprop-1-en-yl)-2,2-dimethylcyclopropanecarboxylic acid (74609-46-4) → 3-(2-chloro-3,3,3-trifluoroprop-1-enyl)-2,2-dimethyl-N-[5-(3,4,5-trimethoxyphenyl)-1,3,4-thiadiazol-2-yl]cyclopropanecarboxamide (1019855-22-1)

Guidance literature:

With O-phenyl phosphorodichloridate; triethylamine; In dichloromethane; at 0 - 5 ℃; Inert atmosphere;

DOI:10.3184/030823410X12889042123874

Reference yield:

Eudesmic acid (118-41-2) → 3-(2-chloro-3,3,3-trifluoroprop-1-enyl)-2,2-dimethyl-N-[5-(3,4,5-trimethoxyphenyl)-1,3,4-thiadiazol-2-yl]cyclopropanecarboxamide (1019855-22-1)

Guidance literature:

Multi-step reaction with 2 steps

1: trichlorophosphate / 0 °C / Reflux; Inert atmosphere

2: O-phenyl phosphorodichloridate; triethylamine / dichloromethane / 0 - 5 °C / Inert atmosphere

With O-phenyl phosphorodichloridate; triethylamine; trichlorophosphate; In dichloromethane;

DOI:10.3184/030823410X12889042123874

upstream raw materials:

2-(3,4,5-trimethoxyphenyl)-5-amino-1,3,4-thiadiazole

3-(2-chloro-3,3,3-trifluoroprop-1-en-yl)-2,2-dimethylcyclopropanecarboxylic acid

Eudesmic acid