(+/-)-3-(4-(1-(3-methyl-4-(4-(trifluoromethyl)-1H-imidazol-1-yl)phenylamino)butyl)benzamido)propanoic acid

Base Information

Chemical Name:(+/-)-3-(4-(1-(3-methyl-4-(4-(trifluoromethyl)-1H-imidazol-1-yl)phenylamino)butyl)benzamido)propanoic acid
CAS No.:1393122-53-6
Molecular Formula:C₂₅H₂₇F₃N₄O₃
Molecular Weight:488.51
Hs Code.:

Synonyms:(+/-)-3-(4-(1-(3-methyl-4-(4-(trifluoromethyl)-1H-imidazol-1-yl)phenylamino)butyl)benzamido)propanoic acid

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Chemical Property of (+/-)-3-(4-(1-(3-methyl-4-(4-(trifluoromethyl)-1H-imidazol-1-yl)phenylamino)butyl)benzamido)propanoic acid

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Technology Process of (+/-)-3-(4-(1-(3-methyl-4-(4-(trifluoromethyl)-1H-imidazol-1-yl)phenylamino)butyl)benzamido)propanoic acid

There total 6 articles about (+/-)-3-(4-(1-(3-methyl-4-(4-(trifluoromethyl)-1H-imidazol-1-yl)phenylamino)butyl)benzamido)propanoic acid 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: 16.0%

: 1393126-54-9
tert-butyl 3-(4-(1-(3-methyl-4-(4-(4-(trifluoromethyl)-1H-imidazol-1-yl)phenyl)amino)butyl)benzamido)propanoate

: 1393122-53-6
(+/-)-3-(4-(1-(3-methyl-4-(4-(trifluoromethyl)-1H-imidazol-1-yl)phenylamino)butyl)benzamido)propanoic acid

Guidance literature:: With trifluoroacetic acid; In dichloromethane; at 20 ℃;

Reference yield:

: 455-88-9
5-nitro-2-fluorotoluene

: 1393122-53-6
(+/-)-3-(4-(1-(3-methyl-4-(4-(trifluoromethyl)-1H-imidazol-1-yl)phenylamino)butyl)benzamido)propanoic acid

Guidance literature:: Multi-step reaction with 6 steps

1: potassium carbonate / acetonitrile / 24 h / 85 °C

2: hydrogen / palladium 10% on activated carbon / ethanol / 6 h / 2482.38 Torr

3: decaborane / methanol / 20 °C / Inert atmosphere

4: water; lithium hydroxide / tetrahydrofuran; methanol / 60 h / 20 °C

5: N-ethyl-N,N-diisopropylamine; HATU / N,N-dimethyl-formamide / 4 h / 20 °C

6: trifluoroacetic acid / dichloromethane / 20 °C

With decaborane; water; hydrogen; potassium carbonate; N-ethyl-N,N-diisopropylamine; HATU; trifluoroacetic acid; lithium hydroxide; palladium 10% on activated carbon; In tetrahydrofuran; methanol; ethanol; dichloromethane; N,N-dimethyl-formamide; acetonitrile;

Reference yield:

: 1393125-28-4
1-(2-methyl-4-nitrophenyl)-4-(trifluoromethyl)-1H-imidazole

: 1393122-53-6
(+/-)-3-(4-(1-(3-methyl-4-(4-(trifluoromethyl)-1H-imidazol-1-yl)phenylamino)butyl)benzamido)propanoic acid

Guidance literature:: Multi-step reaction with 5 steps

1: hydrogen / palladium 10% on activated carbon / ethanol / 6 h / 2482.38 Torr

2: decaborane / methanol / 20 °C / Inert atmosphere

3: water; lithium hydroxide / tetrahydrofuran; methanol / 60 h / 20 °C

4: N-ethyl-N,N-diisopropylamine; HATU / N,N-dimethyl-formamide / 4 h / 20 °C

5: trifluoroacetic acid / dichloromethane / 20 °C

With decaborane; water; hydrogen; N-ethyl-N,N-diisopropylamine; HATU; trifluoroacetic acid; lithium hydroxide; palladium 10% on activated carbon; In tetrahydrofuran; methanol; ethanol; dichloromethane; N,N-dimethyl-formamide;