1-{4-[5-(3-chloro-4-isobutylphenyl)-[1,2,4]-oxadiazol-3-yl]-benzyl}-4-methylpiperidine-4-carboxylic acid ethyl ester

Base Information

Chemical Name:1-{4-[5-(3-chloro-4-isobutylphenyl)-[1,2,4]-oxadiazol-3-yl]-benzyl}-4-methylpiperidine-4-carboxylic acid ethyl ester
CAS No.:1403234-03-6
Molecular Formula:C₂₈H₃₄ClN₃O₃
Molecular Weight:496.049
Hs Code.:

Synonyms:1-{4-[5-(3-chloro-4-isobutylphenyl)-[1,2,4]-oxadiazol-3-yl]-benzyl}-4-methylpiperidine-4-carboxylic acid ethyl ester

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Chemical Property of 1-{4-[5-(3-chloro-4-isobutylphenyl)-[1,2,4]-oxadiazol-3-yl]-benzyl}-4-methylpiperidine-4-carboxylic acid ethyl ester

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Technology Process of 1-{4-[5-(3-chloro-4-isobutylphenyl)-[1,2,4]-oxadiazol-3-yl]-benzyl}-4-methylpiperidine-4-carboxylic acid ethyl ester

There total 8 articles about 1-{4-[5-(3-chloro-4-isobutylphenyl)-[1,2,4]-oxadiazol-3-yl]-benzyl}-4-methylpiperidine-4-carboxylic acid ethyl ester 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:

: 103039-88-9
ethyl 4-methylpiperidine-4-carboxylate

: 1403234-02-5
5-(3-chloro-4-isobutylphenyl)-3-(4-chloromethylphenyl)-[1,2,4]-oxadiazole

: 1403234-03-6
1-{4-[5-(3-chloro-4-isobutylphenyl)-[1,2,4]-oxadiazol-3-yl]-benzyl}-4-methylpiperidine-4-carboxylic acid ethyl ester

Guidance literature:: With potassium carbonate; In N,N-dimethyl-formamide; at 65 - 70 ℃; for 2h;

Reference yield:

: 40150-98-9
4-(2-methyl-1-propyl)benzaldehyde

: 1403234-03-6
1-{4-[5-(3-chloro-4-isobutylphenyl)-[1,2,4]-oxadiazol-3-yl]-benzyl}-4-methylpiperidine-4-carboxylic acid ethyl ester

Guidance literature:: Multi-step reaction with 6 steps

1.1: nitric acid; sulfuric acid / hexane / 2 h / 0 - 5 °C

2.1: tin(ll) chloride / hydrogenchloride / 0.5 h / 0 - 65 °C

2.2: 0.17 h / 0 - 5 °C

2.3: 0.33 h / 60 - 65 °C

3.1: sodium chlorite; sodium dihydrogenphosphate / water; tert-butyl alcohol / 4 h / 20 °C

4.1: dicyclohexyl-carbodiimide; 1-hydroxybenzotriazol-hydrate / N,N-dimethyl-formamide / 2 h / 120 - 125 °C

5.1: thionyl chloride / dichloromethane; N,N-dimethyl-formamide / 0.5 h / 0 - 45 °C

6.1: potassium carbonate / N,N-dimethyl-formamide / 2 h / 65 - 70 °C

With sodium chlorite; sodium dihydrogenphosphate; thionyl chloride; sulfuric acid; nitric acid; potassium carbonate; 1-hydroxybenzotriazol-hydrate; dicyclohexyl-carbodiimide; tin(ll) chloride; In hydrogenchloride; hexane; dichloromethane; water; N,N-dimethyl-formamide; tert-butyl alcohol;

Reference yield:

: 885706-15-0
3-chloro-4-(2-methylpropyl)benzoic acid

: 1403234-03-6
1-{4-[5-(3-chloro-4-isobutylphenyl)-[1,2,4]-oxadiazol-3-yl]-benzyl}-4-methylpiperidine-4-carboxylic acid ethyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: dicyclohexyl-carbodiimide; 1-hydroxybenzotriazol-hydrate / N,N-dimethyl-formamide / 2 h / 120 - 125 °C

2: thionyl chloride / dichloromethane; N,N-dimethyl-formamide / 0.5 h / 0 - 45 °C

3: potassium carbonate / N,N-dimethyl-formamide / 2 h / 65 - 70 °C

With thionyl chloride; potassium carbonate; 1-hydroxybenzotriazol-hydrate; dicyclohexyl-carbodiimide; In dichloromethane; N,N-dimethyl-formamide;