1-(4-(4-bromo-3,5-dimethoxyphenyl)oxazol-2-yl)-2-methoxy-2-(4-morpholinophenyl)-ethanone

Base Information

Chemical Name:1-(4-(4-bromo-3,5-dimethoxyphenyl)oxazol-2-yl)-2-methoxy-2-(4-morpholinophenyl)-ethanone
CAS No.:1333471-26-3
Molecular Formula:C₂₄H₂₅BrN₂O₆
Molecular Weight:517.376
Hs Code.:

Synonyms:1-(4-(4-bromo-3,5-dimethoxyphenyl)oxazol-2-yl)-2-methoxy-2-(4-morpholinophenyl)-ethanone

Suppliers and Price of 1-(4-(4-bromo-3,5-dimethoxyphenyl)oxazol-2-yl)-2-methoxy-2-(4-morpholinophenyl)-ethanone

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 1-(4-(4-bromo-3,5-dimethoxyphenyl)oxazol-2-yl)-2-methoxy-2-(4-morpholinophenyl)-ethanone

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of 1-(4-(4-bromo-3,5-dimethoxyphenyl)oxazol-2-yl)-2-methoxy-2-(4-morpholinophenyl)-ethanone

There total 7 articles about 1-(4-(4-bromo-3,5-dimethoxyphenyl)oxazol-2-yl)-2-methoxy-2-(4-morpholinophenyl)-ethanone 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: 34.0%

: 1333472-31-3
4-(4-bromo-3,5-dimethoxyphenyl)oxazole

: 1333472-27-7
N,2-dimethoxy-N-methyl-2-(4-morpholinophenyl)acetamide

: 1333471-26-3
1-(4-(4-bromo-3,5-dimethoxyphenyl)oxazol-2-yl)-2-methoxy-2-(4-morpholinophenyl)-ethanone

Guidance literature:: 4-(4-bromo-3,5-dimethoxyphenyl)oxazole; With lithium diisopropyl amide; In tetrahydrofuran; n-heptane; ethylbenzene; at -20 - -10 ℃; for 0.833333h; Inert atmosphere;

N,2-dimethoxy-N-methyl-2-(4-morpholinophenyl)acetamide; In tetrahydrofuran; n-heptane; ethylbenzene; at -20 - 20 ℃; for 21h;

Reference yield:

: 1204-86-0
4-(4-morpholinyl)benzaldehyde

: 1333471-26-3
1-(4-(4-bromo-3,5-dimethoxyphenyl)oxazol-2-yl)-2-methoxy-2-(4-morpholinophenyl)-ethanone

Guidance literature:: Multi-step reaction with 3 steps

1.1: potassium hydroxide / 1,4-dioxane / 18 h

1.2: pH 2

2.1: 4-methyl-morpholine; isobutyl chloroformate / dichloromethane / 0.83 h / Inert atmosphere; Cooling with ice

2.2: 16 h / 20 °C

3.1: lithium diisopropyl amide / n-heptane; tetrahydrofuran; ethylbenzene / 0.83 h / -20 - -10 °C / Inert atmosphere

3.2: 21 h / -20 - 20 °C

With 4-methyl-morpholine; potassium hydroxide; lithium diisopropyl amide; isobutyl chloroformate; In tetrahydrofuran; 1,4-dioxane; n-heptane; dichloromethane; ethylbenzene;

Reference yield:

: (RS)-methoxy-(4-morpholin-4-yl-phenyl)-acetic acid

: 1333471-26-3
1-(4-(4-bromo-3,5-dimethoxyphenyl)oxazol-2-yl)-2-methoxy-2-(4-morpholinophenyl)-ethanone

Guidance literature:: Multi-step reaction with 2 steps

1.1: 4-methyl-morpholine; isobutyl chloroformate / dichloromethane / 0.83 h / Inert atmosphere; Cooling with ice

1.2: 16 h / 20 °C

2.1: lithium diisopropyl amide / n-heptane; tetrahydrofuran; ethylbenzene / 0.83 h / -20 - -10 °C / Inert atmosphere

2.2: 21 h / -20 - 20 °C

With 4-methyl-morpholine; lithium diisopropyl amide; isobutyl chloroformate; In tetrahydrofuran; n-heptane; dichloromethane; ethylbenzene;