1-{4-[5-(4-trifluoromethylphenyl)-1,2,4-oxadiazol-3-yl]benzyl}piperidine-4,4-dicarboxylic acid

Base Information

Chemical Name:1-{4-[5-(4-trifluoromethylphenyl)-1,2,4-oxadiazol-3-yl]benzyl}piperidine-4,4-dicarboxylic acid
CAS No.:1093212-39-5
Molecular Formula:C₂₃H₂₀F₃N₃O₅
Molecular Weight:475.424
Hs Code.:

Synonyms:1-{4-[5-(4-trifluoromethylphenyl)-1,2,4-oxadiazol-3-yl]benzyl}piperidine-4,4-dicarboxylic acid

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Chemical Property of 1-{4-[5-(4-trifluoromethylphenyl)-1,2,4-oxadiazol-3-yl]benzyl}piperidine-4,4-dicarboxylic acid

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Technology Process of 1-{4-[5-(4-trifluoromethylphenyl)-1,2,4-oxadiazol-3-yl]benzyl}piperidine-4,4-dicarboxylic acid

There total 4 articles about 1-{4-[5-(4-trifluoromethylphenyl)-1,2,4-oxadiazol-3-yl]benzyl}piperidine-4,4-dicarboxylic 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:

: 1093214-66-4
1-{4-[5-(4-trifluoromethylphenyl)-1,2,4-oxadiazol-3-yl]benzyl}piperidine-4,4-dicarboxylic acid diethyl ester

: 1093212-39-5
1-{4-[5-(4-trifluoromethylphenyl)-1,2,4-oxadiazol-3-yl]benzyl}piperidine-4,4-dicarboxylic acid

Guidance literature:: 1-{4-[5-(4-trifluoromethylphenyl)-1,2,4-oxadiazol-3-yl]benzyl}piperidine-4,4-dicarboxylic acid diethyl ester; With sodium hydroxide; water; In tetrahydrofuran; ethanol; for 20h; Heating / reflux;

With hydrogenchloride; In water; pH=~ 2;

Reference yield:

: 765962-22-9
diethyl 1-benzylpiperidine-4,4-dicarboxylate

: 1093212-39-5
1-{4-[5-(4-trifluoromethylphenyl)-1,2,4-oxadiazol-3-yl]benzyl}piperidine-4,4-dicarboxylic acid

Guidance literature:: Multi-step reaction with 3 steps

1.1: hydrogen / 5%-palladium/activated carbon / ethanol; water / 3 h / 2068.65 Torr

2.1: methanesulfonyl chloride; triethylamine / dichloromethane / 0.33 h / 0 - 10 °C

2.2: 1 h / 80 °C

3.1: sodium hydroxide; water / tetrahydrofuran; ethanol / 20 h / Heating / reflux

3.2: pH ~ 2

With sodium hydroxide; water; hydrogen; methanesulfonyl chloride; triethylamine; 5%-palladium/activated carbon; In tetrahydrofuran; ethanol; dichloromethane; water;

Reference yield:

: N'-hydroxy-4-(hydroxymethyl)benzimidamide

: 1093212-39-5
1-{4-[5-(4-trifluoromethylphenyl)-1,2,4-oxadiazol-3-yl]benzyl}piperidine-4,4-dicarboxylic acid

Guidance literature:: Multi-step reaction with 3 steps

1.1: benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / water; N,N-dimethyl-formamide / 0.5 h / 20 °C

1.2: 3 h / Heating / reflux

2.1: methanesulfonyl chloride; triethylamine / dichloromethane / 0.33 h / 0 - 10 °C

2.2: 1 h / 80 °C

3.1: sodium hydroxide; water / tetrahydrofuran; ethanol / 20 h / Heating / reflux

3.2: pH ~ 2

With sodium hydroxide; water; benzotriazol-1-ol; methanesulfonyl chloride; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; In tetrahydrofuran; ethanol; dichloromethane; water; N,N-dimethyl-formamide;