6-[4-(2-trifluoromethylbenzoyl)piperazin-1-yl]pyridazine-3-carboxylic acid (2-cyclopropyl-2-hydroxyethyl)amide

Base Information

Chemical Name:6-[4-(2-trifluoromethylbenzoyl)piperazin-1-yl]pyridazine-3-carboxylic acid (2-cyclopropyl-2-hydroxyethyl)amide
CAS No.:840490-75-7
Molecular Formula:C₂₂H₂₄F₃N₅O₃
Molecular Weight:463.459
Hs Code.:

Synonyms:6-[4-(2-trifluoromethylbenzoyl)piperazin-1-yl]pyridazine-3-carboxylic acid (2-cyclopropyl-2-hydroxyethyl)amide

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Chemical Property of 6-[4-(2-trifluoromethylbenzoyl)piperazin-1-yl]pyridazine-3-carboxylic acid (2-cyclopropyl-2-hydroxyethyl)amide

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Technology Process of 6-[4-(2-trifluoromethylbenzoyl)piperazin-1-yl]pyridazine-3-carboxylic acid (2-cyclopropyl-2-hydroxyethyl)amide

There total 4 articles about 6-[4-(2-trifluoromethylbenzoyl)piperazin-1-yl]pyridazine-3-carboxylic acid (2-cyclopropyl-2-hydroxyethyl)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:

: 5096-73-1
6-chloro-pyridazine-3-carboxylic acid

: 840490-75-7
6-[4-(2-trifluoromethylbenzoyl)piperazin-1-yl]pyridazine-3-carboxylic acid (2-cyclopropyl-2-hydroxyethyl)amide

Guidance literature:: Multi-step reaction with 2 steps

1.1: thionyl chloride / 1,4-dioxane / 4 h / Reflux

1.2: 20 °C

2.1: 1,8-diazabicyclo[5.4.0]undec-7-ene; tetra-(n-butyl)ammonium iodide / N,N-dimethyl-formamide / 80 °C

With thionyl chloride; tetra-(n-butyl)ammonium iodide; 1,8-diazabicyclo[5.4.0]undec-7-ene; In 1,4-dioxane; N,N-dimethyl-formamide;

Reference yield:

: 1121-79-5
3-chloro-6-methylpyridazine

: 840490-75-7
6-[4-(2-trifluoromethylbenzoyl)piperazin-1-yl]pyridazine-3-carboxylic acid (2-cyclopropyl-2-hydroxyethyl)amide

Guidance literature:: Multi-step reaction with 3 steps

1.1: potassium dichromate; sulfuric acid / 4 h / 50 °C

2.1: thionyl chloride / 1,4-dioxane / 4 h / Reflux

2.2: 20 °C

3.1: 1,8-diazabicyclo[5.4.0]undec-7-ene; tetra-(n-butyl)ammonium iodide / N,N-dimethyl-formamide / 80 °C

With potassium dichromate; thionyl chloride; sulfuric acid; tetra-(n-butyl)ammonium iodide; 1,8-diazabicyclo[5.4.0]undec-7-ene; In 1,4-dioxane; N,N-dimethyl-formamide;

Reference yield:

: 840491-84-1
4-(2-trifluoromethylbenzoyl)piperazine-1-carboxylic acid t-butyl ester

: 840490-75-7
6-[4-(2-trifluoromethylbenzoyl)piperazin-1-yl]pyridazine-3-carboxylic acid (2-cyclopropyl-2-hydroxyethyl)amide

Guidance literature:: Multi-step reaction with 2 steps

1: trifluoroacetic acid / dichloromethane / 5 h / 20 °C

2: 1,8-diazabicyclo[5.4.0]undec-7-ene; tetra-(n-butyl)ammonium iodide / N,N-dimethyl-formamide / 80 °C

With tetra-(n-butyl)ammonium iodide; 1,8-diazabicyclo[5.4.0]undec-7-ene; trifluoroacetic acid; In dichloromethane; N,N-dimethyl-formamide;