N-[4-(4-trifluoromethyl-piperidin-1-yl)-3-(4-bromophenyl)aminocarbonyl-phenyl]-2,6-dichloro-5-(tert-butylcarbonylamino)methyl-benzamide

Base Information

Chemical Name:N-[4-(4-trifluoromethyl-piperidin-1-yl)-3-(4-bromophenyl)aminocarbonyl-phenyl]-2,6-dichloro-5-(tert-butylcarbonylamino)methyl-benzamide
CAS No.:1294495-06-9
Molecular Formula:C₃₂H₃₂BrCl₂F₃N₄O₃
Molecular Weight:728.436
Hs Code.:

Synonyms:N-[4-(4-trifluoromethyl-piperidin-1-yl)-3-(4-bromophenyl)aminocarbonyl-phenyl]-2,6-dichloro-5-(tert-butylcarbonylamino)methyl-benzamide

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Chemical Property of N-[4-(4-trifluoromethyl-piperidin-1-yl)-3-(4-bromophenyl)aminocarbonyl-phenyl]-2,6-dichloro-5-(tert-butylcarbonylamino)methyl-benzamide

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Technology Process of N-[4-(4-trifluoromethyl-piperidin-1-yl)-3-(4-bromophenyl)aminocarbonyl-phenyl]-2,6-dichloro-5-(tert-butylcarbonylamino)methyl-benzamide

There total 5 articles about N-[4-(4-trifluoromethyl-piperidin-1-yl)-3-(4-bromophenyl)aminocarbonyl-phenyl]-2,6-dichloro-5-(tert-butylcarbonylamino)methyl-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: 3.0%

: 1294496-96-0
2,6-dichloro-3-(tert-butylcarbonylamino-methyl)-benzoic acid

: 1294497-39-4
5-amino-N-(4-bromo-phenyl)-2-(4-trifluoromethyl-piperidin-1-yl)-benzamide

: 1294495-06-9
N-[4-(4-trifluoromethyl-piperidin-1-yl)-3-(4-bromophenyl)aminocarbonyl-phenyl]-2,6-dichloro-5-(tert-butylcarbonylamino)methyl-benzamide

Guidance literature:: 2,6-dichloro-3-(tert-butylcarbonylamino-methyl)-benzoic acid; With thionyl chloride; for 2h; Reflux;

5-amino-N-(4-bromo-phenyl)-2-(4-trifluoromethyl-piperidin-1-yl)-benzamide; With N-ethyl-N,N-diisopropylamine; In acetonitrile; at 60 ℃;

Reference yield:

: 50-30-6
2,6-dichlorobenzoic acid

: 1294495-06-9
N-[4-(4-trifluoromethyl-piperidin-1-yl)-3-(4-bromophenyl)aminocarbonyl-phenyl]-2,6-dichloro-5-(tert-butylcarbonylamino)methyl-benzamide

Guidance literature:: Multi-step reaction with 4 steps

1.1: sulfuric acid / 20 °C

2.1: sodium hydroxide; water / methanol / 4 h / 20 °C

3.1: pyridine / acetonitrile / 72 h / 20 °C

4.1: thionyl chloride / 2 h / Reflux

4.2: 60 °C

With pyridine; thionyl chloride; sulfuric acid; water; sodium hydroxide; In methanol; acetonitrile;

Reference yield:

: 3282-30-2
pivaloyl chloride

: 1294495-06-9
N-[4-(4-trifluoromethyl-piperidin-1-yl)-3-(4-bromophenyl)aminocarbonyl-phenyl]-2,6-dichloro-5-(tert-butylcarbonylamino)methyl-benzamide

Guidance literature:: Multi-step reaction with 2 steps

1.1: pyridine / acetonitrile / 72 h / 20 °C

2.1: thionyl chloride / 2 h / Reflux

2.2: 60 °C

With pyridine; thionyl chloride; In acetonitrile;