3-{(S)-{[2-chloro-3-(trifluoromethyl)benzoyl]amino}-[(2S)-piperidin-2-yl]methyl}phenyl trifluoromethanesulfonate

Base Information

Chemical Name:3-{(S)-{[2-chloro-3-(trifluoromethyl)benzoyl]amino}-[(2S)-piperidin-2-yl]methyl}phenyl trifluoromethanesulfonate
CAS No.:1007109-46-7
Molecular Formula:C₂₄H₂₃ClF₆N₂O₄S
Molecular Weight:584.967
Hs Code.:

Synonyms:3-{(S)-{[2-chloro-3-(trifluoromethyl)benzoyl]amino}-[(2S)-piperidin-2-yl]methyl}phenyl trifluoromethanesulfonate

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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 3-{(S)-{[2-chloro-3-(trifluoromethyl)benzoyl]amino}-[(2S)-piperidin-2-yl]methyl}phenyl trifluoromethanesulfonate

Chemical Property:

Purity/Quality:: 98% ^*data from raw suppliers

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Technology Process of 3-{(S)-{[2-chloro-3-(trifluoromethyl)benzoyl]amino}-[(2S)-piperidin-2-yl]methyl}phenyl trifluoromethanesulfonate

There total 9 articles about 3-{(S)-{[2-chloro-3-(trifluoromethyl)benzoyl]amino}-[(2S)-piperidin-2-yl]methyl}phenyl trifluoromethanesulfonate 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: 88.0%

: 1007109-48-9
N-((S)-((2S)-1-allylpiperidin-2-yl)(3-hydroxyphenyl)methyl)-2-chloro-3-(trifluoromethyl)benzamide

: 358-23-6
trifluoromethylsulfonic anhydride

: 1007109-46-7
3-{(S)-{[2-chloro-3-(trifluoromethyl)benzoyl]amino}-[(2S)-piperidin-2-yl]methyl}phenyl trifluoromethanesulfonate

Guidance literature:: With pyridine; In chloroform; at 0 - 20 ℃; for 2h;
DOI:10.1248/cpb.c16-00314

Reference yield:

: 1007109-29-6
tert-butyl (2S)-{(S)-hydroxy(3-methoxyphenyl)methyl}-piperidine-1-carboxylate

: 1007109-46-7
3-{(S)-{[2-chloro-3-(trifluoromethyl)benzoyl]amino}-[(2S)-piperidin-2-yl]methyl}phenyl trifluoromethanesulfonate

Guidance literature:: Multi-step reaction with 6 steps

1.1: potassium hydroxide / methanol; water / 16 h / Reflux

2.1: potassium carbonate / N,N-dimethyl-formamide / 2 h

3.1: methanesulfonyl chloride; triethylamine / chloroform / 2.5 h / 20 °C

3.2: 1 h / 40 °C

4.1: benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / N,N-dimethyl-formamide / 0.5 h

4.2: 3 h

5.1: chloroform; boron tribromide / 1.5 h / Cooling with ice

6.1: pyridine / chloroform / 2 h / 0 - 20 °C

With pyridine; chloroform; boron tribromide; potassium carbonate; benzotriazol-1-ol; methanesulfonyl chloride; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; potassium hydroxide; In methanol; chloroform; water; N,N-dimethyl-formamide;
DOI:10.1248/cpb.c16-00314

Reference yield:

: 1007109-39-8
(S)-(3-methoxyphenyl)((2S)-piperidin-2-yl)methanol

: 1007109-46-7
3-{(S)-{[2-chloro-3-(trifluoromethyl)benzoyl]amino}-[(2S)-piperidin-2-yl]methyl}phenyl trifluoromethanesulfonate

Guidance literature:: Multi-step reaction with 5 steps

1.1: potassium carbonate / N,N-dimethyl-formamide / 2 h

2.1: methanesulfonyl chloride; triethylamine / chloroform / 2.5 h / 20 °C

2.2: 1 h / 40 °C

3.1: benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / N,N-dimethyl-formamide / 0.5 h

3.2: 3 h

4.1: chloroform; boron tribromide / 1.5 h / Cooling with ice

5.1: pyridine / chloroform / 2 h / 0 - 20 °C

With pyridine; chloroform; boron tribromide; potassium carbonate; benzotriazol-1-ol; methanesulfonyl chloride; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; In chloroform; N,N-dimethyl-formamide;
DOI:10.1248/cpb.c16-00314