4-(5-{[4-(propylsulfonyl)-1-piperazinyl]methyl}-1H-tetrazol-1-yl)-2-(trifluoromethyl)benzonitrile

Base Information

Chemical Name:4-(5-{[4-(propylsulfonyl)-1-piperazinyl]methyl}-1H-tetrazol-1-yl)-2-(trifluoromethyl)benzonitrile
CAS No.:1354946-97-6
Molecular Formula:C₁₇H₂₀F₃N₇O₂S
Molecular Weight:443.453
Hs Code.:

Synonyms:4-(5-{[4-(propylsulfonyl)-1-piperazinyl]methyl}-1H-tetrazol-1-yl)-2-(trifluoromethyl)benzonitrile

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Chemical Property of 4-(5-{[4-(propylsulfonyl)-1-piperazinyl]methyl}-1H-tetrazol-1-yl)-2-(trifluoromethyl)benzonitrile

Chemical Property:

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Technology Process of 4-(5-{[4-(propylsulfonyl)-1-piperazinyl]methyl}-1H-tetrazol-1-yl)-2-(trifluoromethyl)benzonitrile

There total 7 articles about 4-(5-{[4-(propylsulfonyl)-1-piperazinyl]methyl}-1H-tetrazol-1-yl)-2-(trifluoromethyl)benzonitrile 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:

: 10147-36-1
n-propanesulfonyl chloride

: 1354946-92-1
4-[5-(1-piperazinylmethyl)-1H-tetrazol-1-yl]-2-(trifluoromethyl)benzonitrile

: 1354946-97-6
4-(5-{[4-(propylsulfonyl)-1-piperazinyl]methyl}-1H-tetrazol-1-yl)-2-(trifluoromethyl)benzonitrile

Guidance literature:: With triethylamine; In dichloromethane; at 20 ℃; for 2.5h; Inert atmosphere;

Reference yield:

: 654-70-6
4-amino-2-trifluoromethylbenzonitrile

: 1354946-97-6
4-(5-{[4-(propylsulfonyl)-1-piperazinyl]methyl}-1H-tetrazol-1-yl)-2-(trifluoromethyl)benzonitrile

Guidance literature:: Multi-step reaction with 7 steps

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

2.1: triphenylphosphine; di-isopropyl azodicarboxylate / tetrahydrofuran / 0.5 h / 0 °C

2.2: 4 h / Reflux

3.1: water; lithium hydroxide / ethanol / 3 h / 0 - 20 °C

4.1: thionyl chloride / toluene / 2 h / Reflux

5.1: triethylamine / acetonitrile / 0.33 h / 120 °C / Microwave irradiation

6.1: hydrogenchloride / 1,4-dioxane; methanol / 1 h / 20 °C

7.1: triethylamine / dichloromethane / 2.5 h / 20 °C / Inert atmosphere

With hydrogenchloride; thionyl chloride; di-isopropyl azodicarboxylate; water; triethylamine; triphenylphosphine; lithium hydroxide; In tetrahydrofuran; 1,4-dioxane; methanol; ethanol; dichloromethane; toluene; acetonitrile;

Reference yield:

: 1354947-70-8
2-{[4-cyano-3-(trifluoromethyl)phenyl]amino}-2-oxoethyl acetate

: 1354946-97-6
4-(5-{[4-(propylsulfonyl)-1-piperazinyl]methyl}-1H-tetrazol-1-yl)-2-(trifluoromethyl)benzonitrile

Guidance literature:: Multi-step reaction with 6 steps

1.1: triphenylphosphine; di-isopropyl azodicarboxylate / tetrahydrofuran / 0.5 h / 0 °C

1.2: 4 h / Reflux

2.1: water; lithium hydroxide / ethanol / 3 h / 0 - 20 °C

3.1: thionyl chloride / toluene / 2 h / Reflux

4.1: triethylamine / acetonitrile / 0.33 h / 120 °C / Microwave irradiation

5.1: hydrogenchloride / 1,4-dioxane; methanol / 1 h / 20 °C

6.1: triethylamine / dichloromethane / 2.5 h / 20 °C / Inert atmosphere

With hydrogenchloride; thionyl chloride; di-isopropyl azodicarboxylate; water; triethylamine; triphenylphosphine; lithium hydroxide; In tetrahydrofuran; 1,4-dioxane; methanol; ethanol; dichloromethane; toluene; acetonitrile;