3-((3-((4-(piperidin-1-yl)-2-((2-(3-(trifluoromethyl)phenyl)pyrimidin-5-yl)carbamoyl)phenyl)carbamoyl)benzyl)thio)propanoic acid

Base Information

Chemical Name:3-((3-((4-(piperidin-1-yl)-2-((2-(3-(trifluoromethyl)phenyl)pyrimidin-5-yl)carbamoyl)phenyl)carbamoyl)benzyl)thio)propanoic acid
CAS No.:1354652-58-6
Molecular Formula:C₃₄H₃₂F₃N₅O₄S
Molecular Weight:663.72
Hs Code.:

Synonyms:3-((3-((4-(piperidin-1-yl)-2-((2-(3-(trifluoromethyl)phenyl)pyrimidin-5-yl)carbamoyl)phenyl)carbamoyl)benzyl)thio)propanoic acid

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Chemical Property of 3-((3-((4-(piperidin-1-yl)-2-((2-(3-(trifluoromethyl)phenyl)pyrimidin-5-yl)carbamoyl)phenyl)carbamoyl)benzyl)thio)propanoic acid

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Technology Process of 3-((3-((4-(piperidin-1-yl)-2-((2-(3-(trifluoromethyl)phenyl)pyrimidin-5-yl)carbamoyl)phenyl)carbamoyl)benzyl)thio)propanoic acid

There total 9 articles about 3-((3-((4-(piperidin-1-yl)-2-((2-(3-(trifluoromethyl)phenyl)pyrimidin-5-yl)carbamoyl)phenyl)carbamoyl)benzyl)thio)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: 80.0%

: 1354652-85-9
methyl 3-(3-((4-(piperidin-1-yl)-2-((2-(3-(trifluoromethyl)phenyl)pyrimidin-5-yl)carbamoyl)phenyl)carbamoyl)-benzylthio)propanoate

: 1354652-58-6
3-((3-((4-(piperidin-1-yl)-2-((2-(3-(trifluoromethyl)phenyl)pyrimidin-5-yl)carbamoyl)phenyl)carbamoyl)benzyl)thio)propanoic acid

Guidance literature:: methyl 3-(3-((4-(piperidin-1-yl)-2-((2-(3-(trifluoromethyl)phenyl)pyrimidin-5-yl)carbamoyl)phenyl)carbamoyl)-benzylthio)propanoate; With lithium hydroxide monohydrate; water; In tetrahydrofuran; at 20 ℃;

With hydrogenchloride; In water; pH=5 - 6;

Reference yield:

: 6515-58-8
3-bromomethylbenzoic acid

: 1354652-58-6
3-((3-((4-(piperidin-1-yl)-2-((2-(3-(trifluoromethyl)phenyl)pyrimidin-5-yl)carbamoyl)phenyl)carbamoyl)benzyl)thio)propanoic acid

Guidance literature:: Multi-step reaction with 6 steps

1.1: ethanol / 20 °C

2.1: potassium carbonate; water / methanol / 4 h / 60 °C

2.2: pH 3

3.1: 1,8-diazabicyclo[5.4.0]undec-7-ene / acetonitrile / Inert atmosphere; Reflux

4.1: oxalyl dichloride / N,N-dimethyl-formamide / dichloromethane / 0.5 h / Inert atmosphere; Reflux

5.1: pyridine / tetrahydrofuran / 4 h / 20 °C

6.1: water; lithium hydroxide monohydrate / tetrahydrofuran / 20 °C

6.2: pH 5 - 6

With pyridine; oxalyl dichloride; lithium hydroxide monohydrate; water; potassium carbonate; 1,8-diazabicyclo[5.4.0]undec-7-ene; N,N-dimethyl-formamide; In tetrahydrofuran; methanol; ethanol; dichloromethane; acetonitrile;

Reference yield:

: 1423-26-3
(meta-(trifluoromethyl)phenyl)boronic acid

: 1354652-58-6
3-((3-((4-(piperidin-1-yl)-2-((2-(3-(trifluoromethyl)phenyl)pyrimidin-5-yl)carbamoyl)phenyl)carbamoyl)benzyl)thio)propanoic acid

Guidance literature:: Multi-step reaction with 5 steps

1.1: potassium carbonate / palladium diacetate; 1,1'-bis-(diphenylphosphino)ferrocene / 100 °C

2.1: dmap; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / dichloromethane / 48 h / 20 °C

3.1: hydrogen / palladium on activated charcoal / ethyl acetate; methanol / 2 h / 20 °C

4.1: pyridine / tetrahydrofuran / 4 h / 20 °C

5.1: water; lithium hydroxide monohydrate / tetrahydrofuran / 20 °C

5.2: pH 5 - 6

With pyridine; dmap; lithium hydroxide monohydrate; water; hydrogen; potassium carbonate; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; 1,1'-bis-(diphenylphosphino)ferrocene; palladium on activated charcoal; palladium diacetate; In tetrahydrofuran; methanol; dichloromethane; ethyl acetate;