7-(2-oxoazepane-1-carbonyl)-2-(4-(2-oxoazepane-1-carbonyl)phenyl)-4H-benzo[d][1,3]oxazin-4-one

Base Information

Chemical Name:7-(2-oxoazepane-1-carbonyl)-2-(4-(2-oxoazepane-1-carbonyl)phenyl)-4H-benzo[d][1,3]oxazin-4-one
CAS No.:1428977-00-7
Molecular Formula:C₂₈H₂₇N₃O₆
Molecular Weight:501.539
Hs Code.:

Synonyms:7-(2-oxoazepane-1-carbonyl)-2-(4-(2-oxoazepane-1-carbonyl)phenyl)-4H-benzo[d][1,3]oxazin-4-one

Suppliers and Price of 7-(2-oxoazepane-1-carbonyl)-2-(4-(2-oxoazepane-1-carbonyl)phenyl)-4H-benzo[d][1,3]oxazin-4-one

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 1 raw suppliers

Chemical Property of 7-(2-oxoazepane-1-carbonyl)-2-(4-(2-oxoazepane-1-carbonyl)phenyl)-4H-benzo[d][1,3]oxazin-4-one

Chemical Property:

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

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of 7-(2-oxoazepane-1-carbonyl)-2-(4-(2-oxoazepane-1-carbonyl)phenyl)-4H-benzo[d][1,3]oxazin-4-one

There total 6 articles about 7-(2-oxoazepane-1-carbonyl)-2-(4-(2-oxoazepane-1-carbonyl)phenyl)-4H-benzo[d][1,3]oxazin-4-one 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:

: 105-60-2,9012-16-2
caprolactam

: 1443648-58-5
C₁₆H₇Cl₂NO₄

: 1428977-00-7
7-(2-oxoazepane-1-carbonyl)-2-(4-(2-oxoazepane-1-carbonyl)phenyl)-4H-benzo[d][1,3]oxazin-4-one

Guidance literature:: With triethylamine; In toluene; at 80 ℃; for 3h; Reflux;
DOI:10.1016/j.tet.2013.03.024

Reference yield:

: 10312-55-7
3-aminoterephthalic acid

: 1428977-00-7
7-(2-oxoazepane-1-carbonyl)-2-(4-(2-oxoazepane-1-carbonyl)phenyl)-4H-benzo[d][1,3]oxazin-4-one

Guidance literature:: Multi-step reaction with 5 steps

1: triethylamine / N,N-dimethyl acetamide / 1.5 h / 20 °C / Cooling with ice

2: potassium hydroxide; water / methanol / 2 h / 60 °C

3: acetic anhydride / 2 h / Reflux

4: thionyl chloride; N,N-dimethyl-formamide / 80 °C

5: triethylamine / toluene / 3 h / 80 °C / Reflux

With thionyl chloride; water; acetic anhydride; triethylamine; N,N-dimethyl-formamide; potassium hydroxide; In methanol; N,N-dimethyl acetamide; toluene;
DOI:10.1016/j.tet.2013.03.024

Reference yield:

: 1428976-99-1
2-(4-сarboxyphenyl)-4-oxo-4H-benzo[d][1,3]oxazine-7-carboxylic acid

: 1428977-00-7
7-(2-oxoazepane-1-carbonyl)-2-(4-(2-oxoazepane-1-carbonyl)phenyl)-4H-benzo[d][1,3]oxazin-4-one

Guidance literature:: Multi-step reaction with 2 steps

1: thionyl chloride; N,N-dimethyl-formamide / 80 °C

2: triethylamine / toluene / 3 h / 80 °C / Reflux

With thionyl chloride; triethylamine; N,N-dimethyl-formamide; In toluene;
DOI:10.1016/j.tet.2013.03.024