N-(3,5-bis(trifluoromethyl)benzyl)-4-chloro-N-((4-phenylpyridin-3-yl)methyl)benzamide

Base Information

Chemical Name:N-(3,5-bis(trifluoromethyl)benzyl)-4-chloro-N-((4-phenylpyridin-3-yl)methyl)benzamide
CAS No.:1491169-24-4
Molecular Formula:C₂₈H₁₉ClF₆N₂O
Molecular Weight:548.915
Hs Code.:

Synonyms:N-(3,5-bis(trifluoromethyl)benzyl)-4-chloro-N-((4-phenylpyridin-3-yl)methyl)benzamide

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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 N-(3,5-bis(trifluoromethyl)benzyl)-4-chloro-N-((4-phenylpyridin-3-yl)methyl)benzamide

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Technology Process of N-(3,5-bis(trifluoromethyl)benzyl)-4-chloro-N-((4-phenylpyridin-3-yl)methyl)benzamide

There total 7 articles about N-(3,5-bis(trifluoromethyl)benzyl)-4-chloro-N-((4-phenylpyridin-3-yl)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: 59.0%

: 1491169-01-7
N-(3,5-bis(trifluoromethyl)benzyl)-1-(4-phenylpyridin-3-yl)methanamine

: 122-01-0
4-chloro-benzoyl chloride

: 1491169-24-4
N-(3,5-bis(trifluoromethyl)benzyl)-4-chloro-N-((4-phenylpyridin-3-yl)methyl)benzamide

Guidance literature:: With triethylamine; In dichloromethane; at 20 ℃;
DOI:10.1016/j.ejmech.2013.07.050

Reference yield:

: 401-95-6
3,5-Bis(trifluoromethyl)benzaldehyde

: 1491169-24-4
N-(3,5-bis(trifluoromethyl)benzyl)-4-chloro-N-((4-phenylpyridin-3-yl)methyl)benzamide

Guidance literature:: Multi-step reaction with 2 steps

1: titanium(IV) isopropylate; triethylamine / dichloromethane / 4 h / 20 °C / Inert atmosphere

2: triethylamine / dichloromethane / 20 °C

With titanium(IV) isopropylate; triethylamine; In dichloromethane;
DOI:10.1016/j.ejmech.2013.07.050

Reference yield:

: 40541-76-2
Ethyl 4-phenylpyridine-3-carboxylate

: 1491169-24-4
N-(3,5-bis(trifluoromethyl)benzyl)-4-chloro-N-((4-phenylpyridin-3-yl)methyl)benzamide

Guidance literature:: Multi-step reaction with 4 steps

1: diisobutylaluminium hydride / toluene; dichloromethane / 1.5 h / -78 °C / Inert atmosphere

2: [bis(acetoxy)iodo]benzene; 2,2,6,6-Tetramethyl-1-piperidinyloxy free radical / dichloromethane / 20 °C

3: sodium tris(acetoxy)borohydride / dichloromethane / 20 °C

4: triethylamine / dichloromethane / 20 °C

With 2,2,6,6-Tetramethyl-1-piperidinyloxy free radical; [bis(acetoxy)iodo]benzene; sodium tris(acetoxy)borohydride; diisobutylaluminium hydride; triethylamine; In dichloromethane; toluene;
DOI:10.1016/j.ejmech.2013.07.050