(E)-3-(3,4-dichlorophenyl)-1-4-[(E)-3-(3,4,5-trimethoxyphenyl)-2-propenoyl]piperazino-2-propen-1-one

Base Information

• Chemical Name: (E)-3-(3,4-dichlorophenyl)-1-4-[(E)-3-(3,4,5-trimethoxyphenyl)-2-propenoyl]piperazino-2-propen-1-one
• CAS No.: 1352050-88-4
• Molecular Formula: C₂₅H₂₆Cl₂N₂O₅
• Molecular Weight: 505.398
• Mol file: 1352050-88-4.mol

Synonyms:(E)-3-(3,4-dichlorophenyl)-1-4-[(E)-3-(3,4,5-trimethoxyphenyl)-2-propenoyl]piperazino-2-propen-1-one

Chemical Property of (E)-3-(3,4-dichlorophenyl)-1-4-[(E)-3-(3,4,5-trimethoxyphenyl)-2-propenoyl]piperazino-2-propen-1-one

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of (E)-3-(3,4-dichlorophenyl)-1-4-[(E)-3-(3,4,5-trimethoxyphenyl)-2-propenoyl]piperazino-2-propen-1-one

There total 2 articles about (E)-3-(3,4-dichlorophenyl)-1-4-[(E)-3-(3,4,5-trimethoxyphenyl)-2-propenoyl]piperazino-2-propen-1-one 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: 83.0%

N-(3,4,5-trimethoxy cinnamoyl)-piperazine (88053-13-8) + (E)-3,4-dichlorocinnamoyl chloride (39156-98-4,82476-03-7) → (E)-3-(3,4-dichlorophenyl)-1-4-[(E)-3-(3,4,5-trimethoxyphenyl)-2-propenoyl]piperazino-2-propen-1-one (1352050-88-4)

Guidance literature:

With triethylamine; In tetrahydrofuran; at 0 - 20 ℃; for 2h;

DOI:10.2174/157018011797655205

Reference yield:

(E)-3-(3,4,5-trimethoxyphenyl)acryloyl chloride (10263-19-1,89652-61-9) → (E)-3-(3,4-dichlorophenyl)-1-4-[(E)-3-(3,4,5-trimethoxyphenyl)-2-propenoyl]piperazino-2-propen-1-one (1352050-88-4)

Guidance literature:

Multi-step reaction with 3 steps

1: triethylamine / tetrahydrofuran / 2 h / 0 - 20 °C

2: trifluoroacetic acid / dichloromethane / 12 h / Inert atmosphere

3: triethylamine / tetrahydrofuran / 2 h / 0 - 20 °C

With triethylamine; trifluoroacetic acid; In tetrahydrofuran; dichloromethane;

DOI:10.2174/157018011797655205

upstream raw materials:

N-(3,4,5-trimethoxy cinnamoyl)-piperazine

(E)-3,4-dichlorocinnamoyl chloride

(E)-3-(3,4,5-trimethoxyphenyl)acryloyl chloride