(S)-4-(5,5-dimethyl-2-oxo-4-phenyloxazolidin-3-yl)-2-methyl-N-(1,5-naphthyridin-4-yl)benzamide

Base Information

Chemical Name:(S)-4-(5,5-dimethyl-2-oxo-4-phenyloxazolidin-3-yl)-2-methyl-N-(1,5-naphthyridin-4-yl)benzamide
CAS No.:1456505-89-7
Molecular Formula:C₂₇H₂₄N₄O₃
Molecular Weight:452.513
Hs Code.:

Synonyms:(S)-4-(5,5-dimethyl-2-oxo-4-phenyloxazolidin-3-yl)-2-methyl-N-(1,5-naphthyridin-4-yl)benzamide

Suppliers and Price of (S)-4-(5,5-dimethyl-2-oxo-4-phenyloxazolidin-3-yl)-2-methyl-N-(1,5-naphthyridin-4-yl)benzamide

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 (S)-4-(5,5-dimethyl-2-oxo-4-phenyloxazolidin-3-yl)-2-methyl-N-(1,5-naphthyridin-4-yl)benzamide

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of (S)-4-(5,5-dimethyl-2-oxo-4-phenyloxazolidin-3-yl)-2-methyl-N-(1,5-naphthyridin-4-yl)benzamide

There total 5 articles about (S)-4-(5,5-dimethyl-2-oxo-4-phenyloxazolidin-3-yl)-2-methyl-N-(1,5-naphthyridin-4-yl)benzamide 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:

: 27392-68-3
4-amino-1,5-naphthyridine

: 1456507-72-4
(S)-4-(5,5-dimethyl-2-oxo-4-phenyloxazolidin-3-yl)-2-methylbenzoyl chloride

: 1456505-89-7
(S)-4-(5,5-dimethyl-2-oxo-4-phenyloxazolidin-3-yl)-2-methyl-N-(1,5-naphthyridin-4-yl)benzamide

Guidance literature:: With N-ethyl-N,N-diisopropylamine; In dichloromethane; at 20 ℃; for 2h;

Reference yield:

: 99548-55-7
4-bromo-2-methyl-benzoic acid methyl ester

: 1456505-89-7
(S)-4-(5,5-dimethyl-2-oxo-4-phenyloxazolidin-3-yl)-2-methyl-N-(1,5-naphthyridin-4-yl)benzamide

Guidance literature:: Multi-step reaction with 4 steps

1: potassium phosphate; N,N`-dimethylethylenediamine; copper(l) iodide / 1,4-dioxane / 1 h / 140 °C / Inert atmosphere; Microwave irradiation; Sealed tube

2: water; lithium hydroxide / methanol; tetrahydrofuran / 16 h / 50 °C

3: thionyl chloride / dichloromethane / 1 h / 40 °C

4: N-ethyl-N,N-diisopropylamine / dichloromethane / 2 h / 20 °C

With potassium phosphate; copper(l) iodide; thionyl chloride; water; N-ethyl-N,N-diisopropylamine; lithium hydroxide; N,N`-dimethylethylenediamine; In tetrahydrofuran; 1,4-dioxane; methanol; dichloromethane;

Reference yield:

: 1456507-70-2
(S)-methyl 4-(5,5-dimethyl-2-oxo-4-phenyloxazolidin-3-yl)-2-methylbenzoate

: 1456505-89-7
(S)-4-(5,5-dimethyl-2-oxo-4-phenyloxazolidin-3-yl)-2-methyl-N-(1,5-naphthyridin-4-yl)benzamide

Guidance literature:: Multi-step reaction with 3 steps

1: water; lithium hydroxide / methanol; tetrahydrofuran / 16 h / 50 °C

2: thionyl chloride / dichloromethane / 1 h / 40 °C

3: N-ethyl-N,N-diisopropylamine / dichloromethane / 2 h / 20 °C

With thionyl chloride; water; N-ethyl-N,N-diisopropylamine; lithium hydroxide; In tetrahydrofuran; methanol; dichloromethane;