(4-(3-amino-4-(1H-tetrazol-1-yl)phenyl)piperazin-1-yl)(phenyl)methanone

Base Information

Chemical Name:(4-(3-amino-4-(1H-tetrazol-1-yl)phenyl)piperazin-1-yl)(phenyl)methanone
CAS No.:1396779-92-2
Molecular Formula:C₁₈H₁₉N₇O
Molecular Weight:349.395
Hs Code.:

Synonyms:(4-(3-amino-4-(1H-tetrazol-1-yl)phenyl)piperazin-1-yl)(phenyl)methanone

Suppliers and Price of (4-(3-amino-4-(1H-tetrazol-1-yl)phenyl)piperazin-1-yl)(phenyl)methanone

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

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Chemicals and raw materials
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price

Total 2 raw suppliers

Chemical Property of (4-(3-amino-4-(1H-tetrazol-1-yl)phenyl)piperazin-1-yl)(phenyl)methanone

Chemical Property:

Purity/Quality:: 98% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

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Technology Process of (4-(3-amino-4-(1H-tetrazol-1-yl)phenyl)piperazin-1-yl)(phenyl)methanone

There total 7 articles about (4-(3-amino-4-(1H-tetrazol-1-yl)phenyl)piperazin-1-yl)(phenyl)methanone 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: 85.0%

: 1396779-90-0
(4-(3-(dibenzylamino)-4-(1H-tetrazol-1-yl)phenyl)piperazin-1-yl)(phenyl)methanone

: 1396779-92-2
(4-(3-amino-4-(1H-tetrazol-1-yl)phenyl)piperazin-1-yl)(phenyl)methanone

Guidance literature:: With hydrogenchloride; hydrogen; 5%-palladium/activated carbon; In methanol; Inert atmosphere;

Reference yield:

: 321-23-3
4-bromo-2-fluoronitrobenzene

: 1396779-92-2
(4-(3-amino-4-(1H-tetrazol-1-yl)phenyl)piperazin-1-yl)(phenyl)methanone

Guidance literature:: Multi-step reaction with 7 steps

1: N-ethyl-N,N-diisopropylamine / 1-methyl-pyrrolidin-2-one / 14 h

2: potassium hydroxide / tBu₄NI / toluene / 4 h

3: potassium phosphate / L-proline; copper(l) iodide / dimethyl sulfoxide / 90 °C

4: triethylamine / dichloromethane / 1.25 h / 5 - 20 °C

5: tin(II) chloride hydrate / ethyl acetate / 20 °C

6: sodium azide / acetic acid / 4 h / 90 °C

7: hydrogenchloride; hydrogen / 5%-palladium/activated carbon / methanol / Inert atmosphere

With hydrogenchloride; potassium phosphate; sodium azide; tin(II) chloride hydrate; hydrogen; triethylamine; N-ethyl-N,N-diisopropylamine; potassium hydroxide; copper(l) iodide; 5%-palladium/activated carbon; L-proline; In 1-methyl-pyrrolidin-2-one; methanol; dichloromethane; acetic acid; dimethyl sulfoxide; ethyl acetate; toluene;

Reference yield:

: 1396780-40-7
N, N-dibenzyl-5-bromo-2-nitroaniline

: 1396779-92-2
(4-(3-amino-4-(1H-tetrazol-1-yl)phenyl)piperazin-1-yl)(phenyl)methanone

Guidance literature:: Multi-step reaction with 5 steps

1: potassium phosphate / L-proline; copper(l) iodide / dimethyl sulfoxide / 90 °C

2: triethylamine / dichloromethane / 1.25 h / 5 - 20 °C

3: tin(II) chloride hydrate / ethyl acetate / 20 °C

4: sodium azide / acetic acid / 4 h / 90 °C

5: hydrogenchloride; hydrogen / 5%-palladium/activated carbon / methanol / Inert atmosphere

With hydrogenchloride; potassium phosphate; sodium azide; tin(II) chloride hydrate; hydrogen; triethylamine; copper(l) iodide; 5%-palladium/activated carbon; L-proline; In methanol; dichloromethane; acetic acid; dimethyl sulfoxide; ethyl acetate;