4-(3-(1-(2-(4-(2,4-dimethoxybenzoyl)phenoxy)acetyl)piperidin-4-yl)propyl)-N-(3-methoxyphenyl)piperidine-1-carboxamide

Base Information

Chemical Name:4-(3-(1-(2-(4-(2,4-dimethoxybenzoyl)phenoxy)acetyl)piperidin-4-yl)propyl)-N-(3-methoxyphenyl)piperidine-1-carboxamide
CAS No.:1360860-38-3
Molecular Formula:C₃₈H₄₇N₃O₇
Molecular Weight:657.807
Hs Code.:

Synonyms:4-(3-(1-(2-(4-(2,4-dimethoxybenzoyl)phenoxy)acetyl)piperidin-4-yl)propyl)-N-(3-methoxyphenyl)piperidine-1-carboxamide

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Chemical Property of 4-(3-(1-(2-(4-(2,4-dimethoxybenzoyl)phenoxy)acetyl)piperidin-4-yl)propyl)-N-(3-methoxyphenyl)piperidine-1-carboxamide

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Technology Process of 4-(3-(1-(2-(4-(2,4-dimethoxybenzoyl)phenoxy)acetyl)piperidin-4-yl)propyl)-N-(3-methoxyphenyl)piperidine-1-carboxamide

There total 4 articles about 4-(3-(1-(2-(4-(2,4-dimethoxybenzoyl)phenoxy)acetyl)piperidin-4-yl)propyl)-N-(3-methoxyphenyl)piperidine-1-carboxamide 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: 82.0%

: 1044591-16-3
2-[4-(2,4-dimethoxy-benzoyl)-phenoxy]-1-[4-(3-piperidin-4-yl-propyl)-piperidin-1-yl]-ethanone

: 18908-07-1
3-methoxyphenyl isocyanate

: 1360860-38-3
4-(3-(1-(2-(4-(2,4-dimethoxybenzoyl)phenoxy)acetyl)piperidin-4-yl)propyl)-N-(3-methoxyphenyl)piperidine-1-carboxamide

Guidance literature:: With triethylamine; In dichloromethane; at 0 - 20 ℃;
DOI:10.1111/j.1747-0285.2011.01307.x

Reference yield:

: 99-96-7
4-hydroxy-benzoic acid

: 1360860-38-3
4-(3-(1-(2-(4-(2,4-dimethoxybenzoyl)phenoxy)acetyl)piperidin-4-yl)propyl)-N-(3-methoxyphenyl)piperidine-1-carboxamide

Guidance literature:: Multi-step reaction with 4 steps

1: zinc(II) chloride; trichlorophosphate / 2 h / 60 - 70 °C

2: potassium carbonate / 10 h / Reflux

3: 4-methyl-morpholine; O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate / N,N-dimethyl-formamide / 5 h / 20 °C

4: triethylamine / dichloromethane / 0 - 20 °C

With 4-methyl-morpholine; potassium carbonate; O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate; triethylamine; zinc(II) chloride; trichlorophosphate; In dichloromethane; N,N-dimethyl-formamide; 1: Friedel Crafts acylation;
DOI:10.1111/j.1747-0285.2011.01307.x

Reference yield:

: 75226-98-1
4-(1-Oxo-2',4'-dimethoxybenzyl)phenoxyacetic acid

: 1360860-38-3
4-(3-(1-(2-(4-(2,4-dimethoxybenzoyl)phenoxy)acetyl)piperidin-4-yl)propyl)-N-(3-methoxyphenyl)piperidine-1-carboxamide

Guidance literature:: Multi-step reaction with 2 steps

1: 4-methyl-morpholine; O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate / N,N-dimethyl-formamide / 5 h / 20 °C

2: triethylamine / dichloromethane / 0 - 20 °C

With 4-methyl-morpholine; O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate; triethylamine; In dichloromethane; N,N-dimethyl-formamide;
DOI:10.1111/j.1747-0285.2011.01307.x