3-methoxy-N-[4-[4-(2-methoxyphenyl)piperazin-1-yl]butyl]-4-(pent-4-yn-1-yloxy)benzamide

Base Information

Chemical Name:3-methoxy-N-[4-[4-(2-methoxyphenyl)piperazin-1-yl]butyl]-4-(pent-4-yn-1-yloxy)benzamide
CAS No.:1346263-97-5
Molecular Formula:C₂₈H₃₇N₃O₄
Molecular Weight:479.619
Hs Code.:

Synonyms:3-methoxy-N-[4-[4-(2-methoxyphenyl)piperazin-1-yl]butyl]-4-(pent-4-yn-1-yloxy)benzamide

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Chemical Property of 3-methoxy-N-[4-[4-(2-methoxyphenyl)piperazin-1-yl]butyl]-4-(pent-4-yn-1-yloxy)benzamide

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Technology Process of 3-methoxy-N-[4-[4-(2-methoxyphenyl)piperazin-1-yl]butyl]-4-(pent-4-yn-1-yloxy)benzamide

There total 4 articles about 3-methoxy-N-[4-[4-(2-methoxyphenyl)piperazin-1-yl]butyl]-4-(pent-4-yn-1-yloxy)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: 97.0%

: 1346263-95-3
3-methoxy-4-(pent-4-yn-1-yloxy)benzoic acid

: 21103-33-3
4-[4-(2-methoxyphenyl)piperazin-1-yl]butylamine

: 1346263-97-5
3-methoxy-N-[4-[4-(2-methoxyphenyl)piperazin-1-yl]butyl]-4-(pent-4-yn-1-yloxy)benzamide

Guidance literature:: With 2-(3H-[1,2,3]triazolo[4,5-b]pyridin-3-yl)-1,1,3,3-tetramethylisouronium hexafluorophosphate; N-ethyl-N,N-diisopropylamine; In dichloromethane; N,N-dimethyl-formamide; at 0 - 20 ℃;
DOI:10.1021/jm2009919

Reference yield:

: 14267-92-6
1-chloro-4-pentyne

: 1346263-97-5
3-methoxy-N-[4-[4-(2-methoxyphenyl)piperazin-1-yl]butyl]-4-(pent-4-yn-1-yloxy)benzamide

Guidance literature:: Multi-step reaction with 3 steps

1: potassium carbonate; potassium iodide / acetonitrile / 20 h / Reflux

2: potassium hydroxide / methanol / 1.5 h / 60 °C

3: 2-(3H-[1,2,3]triazolo[4,5-b]pyridin-3-yl)-1,1,3,3-tetramethylisouronium hexafluorophosphate; N-ethyl-N,N-diisopropylamine / dichloromethane; N,N-dimethyl-formamide / 0 - 20 °C

With 2-(3H-[1,2,3]triazolo[4,5-b]pyridin-3-yl)-1,1,3,3-tetramethylisouronium hexafluorophosphate; potassium carbonate; N-ethyl-N,N-diisopropylamine; potassium iodide; potassium hydroxide; In methanol; dichloromethane; N,N-dimethyl-formamide; acetonitrile;
DOI:10.1021/jm2009919

Reference yield:

: 3943-74-6
4-hydroxy-3-methoxybenzoic acid methyl ester

: 1346263-97-5
3-methoxy-N-[4-[4-(2-methoxyphenyl)piperazin-1-yl]butyl]-4-(pent-4-yn-1-yloxy)benzamide

Guidance literature:: Multi-step reaction with 3 steps

1: potassium carbonate; potassium iodide / acetonitrile / 20 h / Reflux

2: potassium hydroxide / methanol / 1.5 h / 60 °C

3: 2-(3H-[1,2,3]triazolo[4,5-b]pyridin-3-yl)-1,1,3,3-tetramethylisouronium hexafluorophosphate; N-ethyl-N,N-diisopropylamine / dichloromethane; N,N-dimethyl-formamide / 0 - 20 °C

With 2-(3H-[1,2,3]triazolo[4,5-b]pyridin-3-yl)-1,1,3,3-tetramethylisouronium hexafluorophosphate; potassium carbonate; N-ethyl-N,N-diisopropylamine; potassium iodide; potassium hydroxide; In methanol; dichloromethane; N,N-dimethyl-formamide; acetonitrile;
DOI:10.1021/jm2009919