5-chloro-2-hydroxy-N-[(2S)-1-oxo-1-[[4-(trifluoromethyl)phenyl]amino]propan-2-yl]benzamide

Base Information

Chemical Name:5-chloro-2-hydroxy-N-[(2S)-1-oxo-1-[[4-(trifluoromethyl)phenyl]amino]propan-2-yl]benzamide
CAS No.:1469996-80-2
Molecular Formula:C₁₇H₁₄ClF₃N₂O₃
Molecular Weight:386.758
Hs Code.:

Synonyms:5-chloro-2-hydroxy-N-[(2S)-1-oxo-1-[[4-(trifluoromethyl)phenyl]amino]propan-2-yl]benzamide

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Chemical Property of 5-chloro-2-hydroxy-N-[(2S)-1-oxo-1-[[4-(trifluoromethyl)phenyl]amino]propan-2-yl]benzamide

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Technology Process of 5-chloro-2-hydroxy-N-[(2S)-1-oxo-1-[[4-(trifluoromethyl)phenyl]amino]propan-2-yl]benzamide

There total 4 articles about 5-chloro-2-hydroxy-N-[(2S)-1-oxo-1-[[4-(trifluoromethyl)phenyl]amino]propan-2-yl]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: 66.0%

: C₂₄H₂₀ClF₃N₂O₃

: 1469996-80-2
5-chloro-2-hydroxy-N-[(2S)-1-oxo-1-[[4-(trifluoromethyl)phenyl]amino]propan-2-yl]benzamide

Guidance literature:: With palladium 10% on activated carbon; hydrogen; In ethyl acetate; for 12h; under 760.051 Torr;
DOI:10.1016/j.ejmech.2013.08.009

Reference yield:

: 52803-75-5
2-(benzyloxy)-5-chlorobenzoic acid

: 1469996-80-2
5-chloro-2-hydroxy-N-[(2S)-1-oxo-1-[[4-(trifluoromethyl)phenyl]amino]propan-2-yl]benzamide

Guidance literature:: Multi-step reaction with 4 steps

1: 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; benzotriazol-1-ol; triethylamine / dichloromethane / 16.5 h / 5 - 20 °C

2: lithium hydroxide monohydrate / 1,4-dioxane; water / 0.75 h / 50 °C

3: 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; benzotriazol-1-ol; triethylamine / dichloromethane / 16.5 h / 5 - 20 °C

4: palladium 10% on activated carbon; hydrogen / ethyl acetate / 12 h / 760.05 Torr

With lithium hydroxide monohydrate; palladium 10% on activated carbon; hydrogen; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; In 1,4-dioxane; dichloromethane; water; ethyl acetate;
DOI:10.1016/j.ejmech.2013.08.009

Reference yield:

: 1469996-54-0
tert-butyl (2S)-2-[[2-(benzyloxy)-5-chlorobenzoyl]amino]propanoate

: 1469996-80-2
5-chloro-2-hydroxy-N-[(2S)-1-oxo-1-[[4-(trifluoromethyl)phenyl]amino]propan-2-yl]benzamide

Guidance literature:: Multi-step reaction with 3 steps

1: lithium hydroxide monohydrate / 1,4-dioxane; water / 0.75 h / 50 °C

2: 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; benzotriazol-1-ol; triethylamine / dichloromethane / 16.5 h / 5 - 20 °C

3: palladium 10% on activated carbon; hydrogen / ethyl acetate / 12 h / 760.05 Torr

With lithium hydroxide monohydrate; palladium 10% on activated carbon; hydrogen; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; In 1,4-dioxane; dichloromethane; water; ethyl acetate;
DOI:10.1016/j.ejmech.2013.08.009