4-[3-(1-butyl-1H-1,2,3-triazol-4-yl)propoxy]-N-[4-[(indan-2-yl)(propyl)amino]butyl]-3-methoxybenzamide

Base Information

Chemical Name:4-[3-(1-butyl-1H-1,2,3-triazol-4-yl)propoxy]-N-[4-[(indan-2-yl)(propyl)amino]butyl]-3-methoxybenzamide
CAS No.:1346263-89-5
Molecular Formula:C₃₃H₄₇N₅O₃
Molecular Weight:561.768
Hs Code.:

Synonyms:4-[3-(1-butyl-1H-1,2,3-triazol-4-yl)propoxy]-N-[4-[(indan-2-yl)(propyl)amino]butyl]-3-methoxybenzamide

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Chemical Property of 4-[3-(1-butyl-1H-1,2,3-triazol-4-yl)propoxy]-N-[4-[(indan-2-yl)(propyl)amino]butyl]-3-methoxybenzamide

Chemical Property:

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Technology Process of 4-[3-(1-butyl-1H-1,2,3-triazol-4-yl)propoxy]-N-[4-[(indan-2-yl)(propyl)amino]butyl]-3-methoxybenzamide

There total 5 articles about 4-[3-(1-butyl-1H-1,2,3-triazol-4-yl)propoxy]-N-[4-[(indan-2-yl)(propyl)amino]butyl]-3-methoxybenzamide 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: 83.0%

: 1194814-34-0
N¹-(2,3-dihydro-1H-inden-2-yl)-N¹-(prop-1-yl)butane-1,4-diamine

: 1346263-94-2
4-[3-(1-butyl-1H-1,2,3-triazol-4-yl)propoxy]-3-methoxybenzoic acid

: 1346263-89-5
4-[3-(1-butyl-1H-1,2,3-triazol-4-yl)propoxy]-N-[4-[(indan-2-yl)(propyl)amino]butyl]-3-methoxybenzamide

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:

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

: 1346263-89-5
4-[3-(1-butyl-1H-1,2,3-triazol-4-yl)propoxy]-N-[4-[(indan-2-yl)(propyl)amino]butyl]-3-methoxybenzamide

Guidance literature:: Multi-step reaction with 4 steps

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

2: copper(ll) sulfate pentahydrate; sodium L-ascorbate / hexane; dichloromethane; water; tert-butyl alcohol / 16 h / 20 °C

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

4: 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 copper(ll) sulfate pentahydrate; 2-(3H-[1,2,3]triazolo[4,5-b]pyridin-3-yl)-1,1,3,3-tetramethylisouronium hexafluorophosphate; potassium carbonate; sodium L-ascorbate; N-ethyl-N,N-diisopropylamine; potassium iodide; potassium hydroxide; In methanol; hexane; dichloromethane; water; N,N-dimethyl-formamide; acetonitrile; tert-butyl alcohol;
DOI:10.1021/jm2009919

Reference yield:

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

: 1346263-89-5
4-[3-(1-butyl-1H-1,2,3-triazol-4-yl)propoxy]-N-[4-[(indan-2-yl)(propyl)amino]butyl]-3-methoxybenzamide

Guidance literature:: Multi-step reaction with 4 steps

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

2: copper(ll) sulfate pentahydrate; sodium L-ascorbate / hexane; dichloromethane; water; tert-butyl alcohol / 16 h / 20 °C

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

4: 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 copper(ll) sulfate pentahydrate; 2-(3H-[1,2,3]triazolo[4,5-b]pyridin-3-yl)-1,1,3,3-tetramethylisouronium hexafluorophosphate; potassium carbonate; sodium L-ascorbate; N-ethyl-N,N-diisopropylamine; potassium iodide; potassium hydroxide; In methanol; hexane; dichloromethane; water; N,N-dimethyl-formamide; acetonitrile; tert-butyl alcohol;
DOI:10.1021/jm2009919