2-(3-tert-butyl-isoxazol-5-yl)-7-trifluoromethyl-5-(2-trifluoromethyl-phenyl)-1H-imidazo[4,5-b]pyridine

Base Information

Chemical Name:2-(3-tert-butyl-isoxazol-5-yl)-7-trifluoromethyl-5-(2-trifluoromethyl-phenyl)-1H-imidazo[4,5-b]pyridine
CAS No.:1332875-22-5
Molecular Formula:C₂₁H₁₆F₆N₄O
Molecular Weight:454.375
Hs Code.:

Synonyms:2-(3-tert-butyl-isoxazol-5-yl)-7-trifluoromethyl-5-(2-trifluoromethyl-phenyl)-1H-imidazo[4,5-b]pyridine

Suppliers and Price of 2-(3-tert-butyl-isoxazol-5-yl)-7-trifluoromethyl-5-(2-trifluoromethyl-phenyl)-1H-imidazo[4,5-b]pyridine

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 2-(3-tert-butyl-isoxazol-5-yl)-7-trifluoromethyl-5-(2-trifluoromethyl-phenyl)-1H-imidazo[4,5-b]pyridine

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of 2-(3-tert-butyl-isoxazol-5-yl)-7-trifluoromethyl-5-(2-trifluoromethyl-phenyl)-1H-imidazo[4,5-b]pyridine

There total 7 articles about 2-(3-tert-butyl-isoxazol-5-yl)-7-trifluoromethyl-5-(2-trifluoromethyl-phenyl)-1H-imidazo[4,5-b]pyridine 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:

: 1332875-27-0
3-tert-butyl-isoxazole-5-carboxylic acid [3-nitro-4-trifluoromethyl-6-(2-trifluoromethyl-phenyl)-pyridin-2-yl]-amide

: 1332875-22-5
2-(3-tert-butyl-isoxazol-5-yl)-7-trifluoromethyl-5-(2-trifluoromethyl-phenyl)-1H-imidazo[4,5-b]pyridine

Guidance literature:: 3-tert-butyl-isoxazole-5-carboxylic acid [3-nitro-4-trifluoromethyl-6-(2-trifluoromethyl-phenyl)-pyridin-2-yl]-amide; With iron; acetic acid; at 100 ℃; for 2h;

With sodium hydrogencarbonate; In water;

Reference yield:

: 1332875-25-8
4-trifluoromethyl-6-(2-trifluoromethyl-phenyl)-pyridin-2-ylamine

: 1332875-22-5
2-(3-tert-butyl-isoxazol-5-yl)-7-trifluoromethyl-5-(2-trifluoromethyl-phenyl)-1H-imidazo[4,5-b]pyridine

Guidance literature:: Multi-step reaction with 4 steps

1.1: sulfuric acid / 0 - 5 °C

1.2: 0 - 10 °C

1.3: pH 10 / Cooling

2.1: tetrahydrofuran; mineral oil / 1 h / 20 °C

3.1: tetrahydrofuran; mineral oil / 1 h / 20 °C

4.1: iron / acetic acid / 2 h / 100 °C

With sulfuric acid; iron; acetic acid; In tetrahydrofuran; mineral oil;

Reference yield:

: 39890-98-7
2,6-dichloro-4-(trifluoromethyl)pyridine

: 1332875-22-5
2-(3-tert-butyl-isoxazol-5-yl)-7-trifluoromethyl-5-(2-trifluoromethyl-phenyl)-1H-imidazo[4,5-b]pyridine

Guidance literature:: Multi-step reaction with 7 steps

1.1: pyridine / 26 h / 110 °C

2.1: caesium carbonate / dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH₂Cl₂ / 1,2-dimethoxyethane; water / 4 h / 80 °C / Inert atmosphere

3.1: hydrogen / 5%-palladium/activated carbon / methanol / 4 h / 20 °C / Inert atmosphere

4.1: sulfuric acid / 0 - 5 °C

4.2: 0 - 10 °C

4.3: pH 10 / Cooling

5.1: tetrahydrofuran; mineral oil / 1 h / 20 °C

6.1: tetrahydrofuran; mineral oil / 1 h / 20 °C

7.1: iron / acetic acid / 2 h / 100 °C

With pyridine; sulfuric acid; hydrogen; iron; caesium carbonate; dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH₂Cl₂; 5%-palladium/activated carbon; acetic acid; In tetrahydrofuran; methanol; 1,2-dimethoxyethane; water; mineral oil; 2.1: Suzuki Coupling;