6-[4-(2-chloro-5-dimethylaminobenzoyl)piperazin-1-yl]pyridazine-3-carboxylic acid (2-cyclopropylethyl)amide

Base Information

• Chemical Name: 6-[4-(2-chloro-5-dimethylaminobenzoyl)piperazin-1-yl]pyridazine-3-carboxylic acid (2-cyclopropylethyl)amide
• CAS No.: 840490-29-1
• Molecular Formula: C₂₃H₂₉ClN₆O₂
• Molecular Weight: 456.975
• Mol file: 840490-29-1.mol

Synonyms:6-[4-(2-chloro-5-dimethylaminobenzoyl)piperazin-1-yl]pyridazine-3-carboxylic acid (2-cyclopropylethyl)amide

Chemical Property of 6-[4-(2-chloro-5-dimethylaminobenzoyl)piperazin-1-yl]pyridazine-3-carboxylic acid (2-cyclopropylethyl)amide

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of 6-[4-(2-chloro-5-dimethylaminobenzoyl)piperazin-1-yl]pyridazine-3-carboxylic acid (2-cyclopropylethyl)amide

There total 5 articles about 6-[4-(2-chloro-5-dimethylaminobenzoyl)piperazin-1-yl]pyridazine-3-carboxylic acid (2-cyclopropylethyl)amide 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: 53.0%

6-piperazin-1-yl-pyridazine-3-carboxylic acid (2-cyclopropylethyl)amide (840488-88-2) + C9H9Cl2NO (1408159-05-6) → 6-[4-(2-chloro-5-dimethylaminobenzoyl)piperazin-1-yl]pyridazine-3-carboxylic acid (2-cyclopropylethyl)amide (840490-29-1)

Guidance literature:

With triethylamine; In dichloromethane; at 0 - 20 ℃; for 1.08333h;

DOI:10.1021/jm301661h

Reference yield: 53.0%

→ 6-[4-(2-chloro-5-dimethylaminobenzoyl)piperazin-1-yl]pyridazine-3-carboxylic acid (2-cyclopropylethyl)amide (840490-29-1)

Guidance literature:

With benzotriazol-1-ol; 1,8-diazabicyclo[5.4.0]undec-7-ene; In N,N-dimethyl-formamide; at 20 ℃; for 0.25h;

With 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In N,N-dimethyl-formamide; at 20 ℃;

Reference yield:

6-chloro-pyridazine-3-carboxylic acid (5096-73-1) → 6-[4-(2-chloro-5-dimethylaminobenzoyl)piperazin-1-yl]pyridazine-3-carboxylic acid (2-cyclopropylethyl)amide (840490-29-1)

Guidance literature:

Multi-step reaction with 4 steps

1: thionyl chloride; N,N-dimethyl-formamide / chloroform / 11 h / Reflux

2: triethylamine / dichloromethane / 0.5 h / 0 - 20 °C

3: acetonitrile / 2 h / Reflux

4: triethylamine / dichloromethane / 1.08 h / 0 - 20 °C

With thionyl chloride; triethylamine; N,N-dimethyl-formamide; In dichloromethane; chloroform; acetonitrile;

DOI:10.1021/jm301661h

upstream raw materials:

6-chloro-pyridazine-3-carboxylic acid

6-chloro-pyridazine-3-carbonyl chloride

6-piperazin-1-yl-pyridazine-3-carboxylic acid (2-cyclopropylethyl)amide

C₉H₉Cl₂NO