1-(4-(4-phenoxybenzyl)piperazine-1-carbonyl)-1H-pyrazole-4-carbonitrile

Base Information

Chemical Name:1-(4-(4-phenoxybenzyl)piperazine-1-carbonyl)-1H-pyrazole-4-carbonitrile
CAS No.:1622426-40-7
Molecular Formula:C₂₂H₂₁N₅O₂
Molecular Weight:387.441
Hs Code.:

Synonyms:1-(4-(4-phenoxybenzyl)piperazine-1-carbonyl)-1H-pyrazole-4-carbonitrile

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Chemical Property of 1-(4-(4-phenoxybenzyl)piperazine-1-carbonyl)-1H-pyrazole-4-carbonitrile

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Technology Process of 1-(4-(4-phenoxybenzyl)piperazine-1-carbonyl)-1H-pyrazole-4-carbonitrile

There total 3 articles about 1-(4-(4-phenoxybenzyl)piperazine-1-carbonyl)-1H-pyrazole-4-carbonitrile 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:

: 274672-75-2
1-(4-phenoxybenzyl)piperazine

: C₅H₂ClN₃O

: 1622426-40-7
1-(4-(4-phenoxybenzyl)piperazine-1-carbonyl)-1H-pyrazole-4-carbonitrile

Guidance literature:: With triethylamine; In dichloromethane; at 0 - 20 ℃; for 16h; Inert atmosphere;
DOI:10.1016/j.bmcl.2014.06.063

Reference yield:

: 1622427-11-5
tert-butyl 4-(4-phenoxybenzyl)piperazine-1-carboxylate

: 1622426-40-7
1-(4-(4-phenoxybenzyl)piperazine-1-carbonyl)-1H-pyrazole-4-carbonitrile

Guidance literature:: Multi-step reaction with 2 steps

1: hydrogenchloride / dichloromethane; 1,4-dioxane / 4 h / 0 - 20 °C / Inert atmosphere

2: triethylamine / dichloromethane / 16 h / 0 - 20 °C / Inert atmosphere

With hydrogenchloride; triethylamine; In 1,4-dioxane; dichloromethane;
DOI:10.1016/j.bmcl.2014.06.063

Reference yield:

: 36881-42-2
1-(bromomethyl)-4-phenoxybenzene

: 1622426-40-7
1-(4-(4-phenoxybenzyl)piperazine-1-carbonyl)-1H-pyrazole-4-carbonitrile

Guidance literature:: Multi-step reaction with 3 steps

1.1: triethylamine / tetrahydrofuran / 0.25 h / Inert atmosphere

1.2: 24 h / 20 °C / Inert atmosphere

2.1: hydrogenchloride / dichloromethane; 1,4-dioxane / 4 h / 0 - 20 °C / Inert atmosphere

3.1: triethylamine / dichloromethane / 16 h / 0 - 20 °C / Inert atmosphere

With hydrogenchloride; triethylamine; In tetrahydrofuran; 1,4-dioxane; dichloromethane;
DOI:10.1016/j.bmcl.2014.06.063