N,2-dimethoxy-N-methyl-2-(4-(5-methyl-1,3,4-oxadiazol-2-yl)phenyl)acetamide

Base Information

Chemical Name:N,2-dimethoxy-N-methyl-2-(4-(5-methyl-1,3,4-oxadiazol-2-yl)phenyl)acetamide
CAS No.:1333472-40-4
Molecular Formula:C₁₄H₁₇N₃O₄
Molecular Weight:291.307
Hs Code.:

Synonyms:N,2-dimethoxy-N-methyl-2-(4-(5-methyl-1,3,4-oxadiazol-2-yl)phenyl)acetamide

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of N,2-dimethoxy-N-methyl-2-(4-(5-methyl-1,3,4-oxadiazol-2-yl)phenyl)acetamide

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Technology Process of N,2-dimethoxy-N-methyl-2-(4-(5-methyl-1,3,4-oxadiazol-2-yl)phenyl)acetamide

There total 2 articles about N,2-dimethoxy-N-methyl-2-(4-(5-methyl-1,3,4-oxadiazol-2-yl)phenyl)acetamide 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: 26.0%

: 1333472-39-1
2-methoxy-2-(4-(5-methyl-1,3,4-oxadiazol-2-yl)phenyl)acetic acid

: 6638-79-5
N,O-dimethylhydroxylamine*hydrochloride

: 1333472-40-4
N,2-dimethoxy-N-methyl-2-(4-(5-methyl-1,3,4-oxadiazol-2-yl)phenyl)acetamide

Guidance literature:: 2-methoxy-2-(4-(5-methyl-1,3,4-oxadiazol-2-yl)phenyl)acetic acid; With N-ethyl-N,N-diisopropylamine; (bis-(2-methoxyethyl)amino)sulfur trufluoride; In dichloromethane; for 0.75h; Inert atmosphere; Cooling with ice;

N,O-dimethylhydroxylamine*hydrochloride; In dichloromethane; for 3.5h; Cooling with ice;

With sodium hydrogencarbonate; In dichloromethane; water; for 0.5h;

Reference yield:

: 179056-82-7
4-(5-methyl-1,3,4-oxadiazol-2-yl)benzaldehyde

: 1333472-40-4
N,2-dimethoxy-N-methyl-2-(4-(5-methyl-1,3,4-oxadiazol-2-yl)phenyl)acetamide

Guidance literature:: Multi-step reaction with 2 steps

1.1: potassium hydroxide / 1,4-dioxane / 20 °C / Cooling with ice

1.2: pH 1

2.1: N-ethyl-N,N-diisopropylamine; (bis-(2-methoxyethyl)amino)sulfur trufluoride / dichloromethane / 0.75 h / Inert atmosphere; Cooling with ice

2.2: 3.5 h / Cooling with ice

2.3: 0.5 h

With N-ethyl-N,N-diisopropylamine; potassium hydroxide; (bis-(2-methoxyethyl)amino)sulfur trufluoride; In 1,4-dioxane; dichloromethane;

Reference yield: 29.0%

: 1225145-74-3
2-(3,4,5-trimethoxyphenyl)furan

: 1333472-40-4
N,2-dimethoxy-N-methyl-2-(4-(5-methyl-1,3,4-oxadiazol-2-yl)phenyl)acetamide

: 1333471-70-7
2-methoxy-2-(4-(5-methyl-1,3,4-oxadiazol-2-yl)phenyl)-1-(5-(3,4,5-trimethoxyphenyl)furan-2-yl)ethanone

Guidance literature:: 2-(3,4,5-trimethoxyphenyl)furan; With n-butyllithium; In tetrahydrofuran; hexanes; at -78 ℃; for 1h; Inert atmosphere;

N,2-dimethoxy-N-methyl-2-(4-(5-methyl-1,3,4-oxadiazol-2-yl)phenyl)acetamide; In tetrahydrofuran; hexanes; at -78 - 20 ℃; for 2.41667h;