6-[1-(4-methoxybenzyl)-1H-pyrazol-4-yl]-1-(2-methyl-5-nitrophenyl)-1H-imidazo-[1,2-b]pyrazole

Base Information

Chemical Name:6-[1-(4-methoxybenzyl)-1H-pyrazol-4-yl]-1-(2-methyl-5-nitrophenyl)-1H-imidazo-[1,2-b]pyrazole
CAS No.:1448317-28-9
Molecular Formula:C₂₃H₂₀N₆O₃
Molecular Weight:428.45
Hs Code.:

Synonyms:6-[1-(4-methoxybenzyl)-1H-pyrazol-4-yl]-1-(2-methyl-5-nitrophenyl)-1H-imidazo-[1,2-b]pyrazole

Suppliers and Price of 6-[1-(4-methoxybenzyl)-1H-pyrazol-4-yl]-1-(2-methyl-5-nitrophenyl)-1H-imidazo-[1,2-b]pyrazole

Supply Marketing:

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

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 0 raw suppliers

Chemical Property of 6-[1-(4-methoxybenzyl)-1H-pyrazol-4-yl]-1-(2-methyl-5-nitrophenyl)-1H-imidazo-[1,2-b]pyrazole

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of 6-[1-(4-methoxybenzyl)-1H-pyrazol-4-yl]-1-(2-methyl-5-nitrophenyl)-1H-imidazo-[1,2-b]pyrazole

There total 5 articles about 6-[1-(4-methoxybenzyl)-1H-pyrazol-4-yl]-1-(2-methyl-5-nitrophenyl)-1H-imidazo-[1,2-b]pyrazole 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:

: 1448317-27-8
1-(2,2-diethoxyethyl)-1'-(4-methoxybenzyl)-N-(2-methyl-5-nitrophenyl)-1H,1'H-3,4'-bipyrazole-5-amine

: 1448317-28-9
6-[1-(4-methoxybenzyl)-1H-pyrazol-4-yl]-1-(2-methyl-5-nitrophenyl)-1H-imidazo-[1,2-b]pyrazole

Guidance literature:: With sulfuric acid; In ethanol; at 120 ℃; for 0.583333h; Microwave irradiation;

Reference yield:

: 2746-25-0
p-Methoxybenzyl bromide

: 1448317-28-9
6-[1-(4-methoxybenzyl)-1H-pyrazol-4-yl]-1-(2-methyl-5-nitrophenyl)-1H-imidazo-[1,2-b]pyrazole

Guidance literature:: Multi-step reaction with 5 steps

1.1: potassium tert-butylate / tetrahydrofuran / 0 - 20 °C

2.1: n-butyllithium / tetrahydrofuran; hexane / 0.25 h / -70 °C

2.2: 1.5 h / -78 - 20 °C

3.1: hydrogenchloride / ethanol; water / 0.75 h / 120 °C / Microwave irradiation

4.1: 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene; palladium diacetate; caesium carbonate / 1,4-dioxane / 0.5 h / 150 °C / Microwave irradiation; Inert atmosphere

5.1: sulfuric acid / ethanol / 0.58 h / 120 °C / Microwave irradiation

With hydrogenchloride; n-butyllithium; sulfuric acid; potassium tert-butylate; palladium diacetate; caesium carbonate; 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene; In tetrahydrofuran; 1,4-dioxane; ethanol; hexane; water;

Reference yield:

: 1448317-16-5
(2E)-3-amino-3-[1-(4-methoxybenzyl)-1H-pyrazol-4-yl]acrylonitrile

: 1448317-28-9
6-[1-(4-methoxybenzyl)-1H-pyrazol-4-yl]-1-(2-methyl-5-nitrophenyl)-1H-imidazo-[1,2-b]pyrazole

Guidance literature:: Multi-step reaction with 3 steps

1: hydrogenchloride / ethanol; water / 0.75 h / 120 °C / Microwave irradiation

2: 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene; palladium diacetate; caesium carbonate / 1,4-dioxane / 0.5 h / 150 °C / Microwave irradiation; Inert atmosphere

3: sulfuric acid / ethanol / 0.58 h / 120 °C / Microwave irradiation

With hydrogenchloride; sulfuric acid; palladium diacetate; caesium carbonate; 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene; In 1,4-dioxane; ethanol; water;