3-bromo-N-{(2S)-2-(4-fluorophenyl)-4-[3-(4-acetylpiperazin-1-yl)azetidin-1-yl]butyl}-N-methyl-5-(trifluoromethyl)benzamide

Base Information

Chemical Name:3-bromo-N-{(2S)-2-(4-fluorophenyl)-4-[3-(4-acetylpiperazin-1-yl)azetidin-1-yl]butyl}-N-methyl-5-(trifluoromethyl)benzamide
CAS No.:930783-06-5
Molecular Formula:C₂₈H₃₃BrF₄N₄O₂
Molecular Weight:613.493
Hs Code.:

Synonyms:3-bromo-N-{(2S)-2-(4-fluorophenyl)-4-[3-(4-acetylpiperazin-1-yl)azetidin-1-yl]butyl}-N-methyl-5-(trifluoromethyl)benzamide

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Chemical Property of 3-bromo-N-{(2S)-2-(4-fluorophenyl)-4-[3-(4-acetylpiperazin-1-yl)azetidin-1-yl]butyl}-N-methyl-5-(trifluoromethyl)benzamide

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Technology Process of 3-bromo-N-{(2S)-2-(4-fluorophenyl)-4-[3-(4-acetylpiperazin-1-yl)azetidin-1-yl]butyl}-N-methyl-5-(trifluoromethyl)benzamide

There total 3 articles about 3-bromo-N-{(2S)-2-(4-fluorophenyl)-4-[3-(4-acetylpiperazin-1-yl)azetidin-1-yl]butyl}-N-methyl-5-(trifluoromethyl)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: 54.0%

: 917572-25-9
3-bromo-N-[(2S)-2-(4-fluorophenyl)-4-oxobutyl]-N-methyl-5-(trifluoromethyl)benzamide

: 1-acetyl-4-azetidin-3-ylpiperazine dihydrochloride

: 930783-06-5
3-bromo-N-{(2S)-2-(4-fluorophenyl)-4-[3-(4-acetylpiperazin-1-yl)azetidin-1-yl]butyl}-N-methyl-5-(trifluoromethyl)benzamide

Guidance literature:: 3-bromo-N-[(2S)-2-(4-fluorophenyl)-4-oxobutyl]-N-methyl-5-(trifluoromethyl)benzamide; 1-acetyl-4-azetidin-3-ylpiperazine dihydrochloride; With triethylamine; In methanol; at 20 ℃; for 0.75h;

With sodium tris(acetoxy)borohydride; In methanol; at 20 ℃; for 1.75h;

With sodium hydroxide; In water; toluene; at 40 - 45 ℃; for 0.0833333h;

Reference yield:

: 235097-95-7
[(2S)-2-(4-fluorophenyl)pent-4-en-1-yl]methylamine

: 930783-06-5
3-bromo-N-{(2S)-2-(4-fluorophenyl)-4-[3-(4-acetylpiperazin-1-yl)azetidin-1-yl]butyl}-N-methyl-5-(trifluoromethyl)benzamide

Guidance literature:: Multi-step reaction with 3 steps

1.1: O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate; N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide / 20 °C

2.1: osmium(VIII) oxide; 4-methylmorpholine N-oxide / acetone; tert-butyl alcohol / 20 °C

2.2: 20 °C

3.1: sodium tris(acetoxy)borohydride; triethylamine / methanol / 0.25 - 0.5 h / 25 - 30 °C

With osmium(VIII) oxide; sodium tris(acetoxy)borohydride; O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate; 4-methylmorpholine N-oxide; triethylamine; N-ethyl-N,N-diisopropylamine; In methanol; N,N-dimethyl-formamide; acetone; tert-butyl alcohol;

Reference yield:

: 328-67-6
3-bromo-5-(trifluoromethyl)benzoic acid

: 930783-06-5
3-bromo-N-{(2S)-2-(4-fluorophenyl)-4-[3-(4-acetylpiperazin-1-yl)azetidin-1-yl]butyl}-N-methyl-5-(trifluoromethyl)benzamide

Guidance literature:: Multi-step reaction with 3 steps

1.1: O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate; N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide / 20 °C

2.1: osmium(VIII) oxide; 4-methylmorpholine N-oxide / acetone; tert-butyl alcohol / 20 °C

2.2: 20 °C

3.1: sodium tris(acetoxy)borohydride; triethylamine / methanol / 0.25 - 0.5 h / 25 - 30 °C

With osmium(VIII) oxide; sodium tris(acetoxy)borohydride; O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate; 4-methylmorpholine N-oxide; triethylamine; N-ethyl-N,N-diisopropylamine; In methanol; N,N-dimethyl-formamide; acetone; tert-butyl alcohol;