4-[2-(5-methyl-2-phenyl-1,3-oxazol-4-yl)ethoxy]-1H-indazole

Base Information

Chemical Name:4-[2-(5-methyl-2-phenyl-1,3-oxazol-4-yl)ethoxy]-1H-indazole
CAS No.:748154-34-9
Molecular Formula:C₁₉H₁₇N₃O₂
Molecular Weight:319.363
Hs Code.:

Synonyms:4-[2-(5-methyl-2-phenyl-1,3-oxazol-4-yl)ethoxy]-1H-indazole

Suppliers and Price of 4-[2-(5-methyl-2-phenyl-1,3-oxazol-4-yl)ethoxy]-1H-indazole

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 4-[2-(5-methyl-2-phenyl-1,3-oxazol-4-yl)ethoxy]-1H-indazole

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of 4-[2-(5-methyl-2-phenyl-1,3-oxazol-4-yl)ethoxy]-1H-indazole

There total 4 articles about 4-[2-(5-methyl-2-phenyl-1,3-oxazol-4-yl)ethoxy]-1H-indazole 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: 77.0%

: 748154-35-0
2-methyl-3-[2-(5-methyl-2-phenyl-1,3-oxazol-4-yl)ethoxy]aniline

: 748154-34-9
4-[2-(5-methyl-2-phenyl-1,3-oxazol-4-yl)ethoxy]-1H-indazole

Guidance literature:: 2-methyl-3-[2-(5-methyl-2-phenyl-1,3-oxazol-4-yl)ethoxy]aniline; With potassium acetate; acetic anhydride; In benzene; at 20 ℃; for 1h;

With isopentyl nitrite; In benzene; for 20h; Heating / reflux;

With potassium carbonate; In methanol; at 20 ℃; for 4h;

Reference yield:

: 105983-77-5
methyl 4-bromo-3-oxopentanoate

: 748154-34-9
4-[2-(5-methyl-2-phenyl-1,3-oxazol-4-yl)ethoxy]-1H-indazole

Guidance literature:: Multi-step reaction with 6 steps

1: toluene-4-sulfonic acid / methanol / Heating

2: diisobutylaluminium hydride

3: N-ethyl-N,N-diisopropylamine / dichloromethane / 18.5 h / 3 - 20 °C / Inert atmosphere; Cooling with ice

4: caesium carbonate / acetonitrile / 18 h / 20 - 60 °C

5: hydrogen; palladium on activated charcoal / methanol; ethyl acetate

6: potassium acetate; acetic anhydride / benzene

With palladium on activated charcoal; hydrogen; potassium acetate; acetic anhydride; diisobutylaluminium hydride; caesium carbonate; toluene-4-sulfonic acid; N-ethyl-N,N-diisopropylamine; In methanol; dichloromethane; ethyl acetate; acetonitrile; benzene;
DOI:10.1021/op0601621

Reference yield:

: 103788-64-3
methyl 2-(5-methyl-2-phenyl-1,3-oxazol-4-yl)acetate

: 748154-34-9
4-[2-(5-methyl-2-phenyl-1,3-oxazol-4-yl)ethoxy]-1H-indazole

Guidance literature:: Multi-step reaction with 5 steps

1: diisobutylaluminium hydride

2: N-ethyl-N,N-diisopropylamine / dichloromethane / 18.5 h / 3 - 20 °C / Inert atmosphere; Cooling with ice

3: caesium carbonate / acetonitrile / 18 h / 20 - 60 °C

4: hydrogen; palladium on activated charcoal / methanol; ethyl acetate

5: potassium acetate; acetic anhydride / benzene

With palladium on activated charcoal; hydrogen; potassium acetate; acetic anhydride; diisobutylaluminium hydride; caesium carbonate; N-ethyl-N,N-diisopropylamine; In methanol; dichloromethane; ethyl acetate; acetonitrile; benzene;
DOI:10.1021/op0601621