2-(1-(2-hydroxy-2-(4-(5-(5-phenyl-4-propylisoxazol-3-yl)-1,2,4-oxadiazol-3-yl)phenyl)ethyl)piperidin-3-yl)acetic acid

Base Information

Chemical Name:2-(1-(2-hydroxy-2-(4-(5-(5-phenyl-4-propylisoxazol-3-yl)-1,2,4-oxadiazol-3-yl)phenyl)ethyl)piperidin-3-yl)acetic acid
CAS No.:1265322-06-2
Molecular Formula:C₂₉H₃₂N₄O₅
Molecular Weight:516.597
Hs Code.:

Synonyms:2-(1-(2-hydroxy-2-(4-(5-(5-phenyl-4-propylisoxazol-3-yl)-1,2,4-oxadiazol-3-yl)phenyl)ethyl)piperidin-3-yl)acetic acid

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Chemical Property of 2-(1-(2-hydroxy-2-(4-(5-(5-phenyl-4-propylisoxazol-3-yl)-1,2,4-oxadiazol-3-yl)phenyl)ethyl)piperidin-3-yl)acetic acid

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Technology Process of 2-(1-(2-hydroxy-2-(4-(5-(5-phenyl-4-propylisoxazol-3-yl)-1,2,4-oxadiazol-3-yl)phenyl)ethyl)piperidin-3-yl)acetic acid

There total 7 articles about 2-(1-(2-hydroxy-2-(4-(5-(5-phenyl-4-propylisoxazol-3-yl)-1,2,4-oxadiazol-3-yl)phenyl)ethyl)piperidin-3-yl)acetic 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:

: 1265323-46-3
2-bromo-1-(4-(5-(5-phenyl-4-propylisoxazol-3-yl)-1,2,4-oxadiazol-3-yl)phenyl)ethanol

: 74494-52-3
3-Piperidinylacetic Acid

: 1265322-06-2
2-(1-(2-hydroxy-2-(4-(5-(5-phenyl-4-propylisoxazol-3-yl)-1,2,4-oxadiazol-3-yl)phenyl)ethyl)piperidin-3-yl)acetic acid

Guidance literature:: 3-Piperidinylacetic Acid; With tetra(n-butyl)ammonium hydroxide; In tetrahydrofuran; dimethyl sulfoxide; at 20 ℃; for 0.25h;

2-bromo-1-(4-(5-(5-phenyl-4-propylisoxazol-3-yl)-1,2,4-oxadiazol-3-yl)phenyl)ethanol; In tetrahydrofuran; dimethyl sulfoxide; at 80 ℃; for 1.5h;

Reference yield:

: 4250-81-1
1-phenyl-1-pentyne

: 1265322-06-2
2-(1-(2-hydroxy-2-(4-(5-(5-phenyl-4-propylisoxazol-3-yl)-1,2,4-oxadiazol-3-yl)phenyl)ethyl)piperidin-3-yl)acetic acid

Guidance literature:: Multi-step reaction with 7 steps

1.1: 18 h / 160 °C

2.1: sodium hydroxide / ethanol / 2 h / 75 °C

3.1: pyridine; trifluoro-[1,3,5]triazine / dichloromethane / 1 h / 20 °C

4.1: N-ethyl-N,N-diisopropylamine / acetonitrile / 70 °C

5.1: 3-chloro-benzenecarboperoxoic acid / dichloromethane / 20 °C

6.1: triethyl-bromo-silane / tetrahydrofuran / 1 h / -78 °C

7.1: tetra(n-butyl)ammonium hydroxide / dimethyl sulfoxide; tetrahydrofuran / 0.25 h / 20 °C

7.2: 1.5 h / 80 °C

With pyridine; trifluoro-[1,3,5]triazine; triethyl-bromo-silane; tetra(n-butyl)ammonium hydroxide; N-ethyl-N,N-diisopropylamine; 3-chloro-benzenecarboperoxoic acid; sodium hydroxide; In tetrahydrofuran; ethanol; dichloromethane; dimethyl sulfoxide; acetonitrile;

Reference yield:

: 1265323-42-9
5-phenyl-4-propylisoxazole-3-carboxylic acid

: 1265322-06-2
2-(1-(2-hydroxy-2-(4-(5-(5-phenyl-4-propylisoxazol-3-yl)-1,2,4-oxadiazol-3-yl)phenyl)ethyl)piperidin-3-yl)acetic acid

Guidance literature:: Multi-step reaction with 5 steps

1.1: pyridine; trifluoro-[1,3,5]triazine / dichloromethane / 1 h / 20 °C

2.1: N-ethyl-N,N-diisopropylamine / acetonitrile / 70 °C

3.1: 3-chloro-benzenecarboperoxoic acid / dichloromethane / 20 °C

4.1: triethyl-bromo-silane / tetrahydrofuran / 1 h / -78 °C

5.1: tetra(n-butyl)ammonium hydroxide / dimethyl sulfoxide; tetrahydrofuran / 0.25 h / 20 °C

5.2: 1.5 h / 80 °C

With pyridine; trifluoro-[1,3,5]triazine; triethyl-bromo-silane; tetra(n-butyl)ammonium hydroxide; N-ethyl-N,N-diisopropylamine; 3-chloro-benzenecarboperoxoic acid; In tetrahydrofuran; dichloromethane; dimethyl sulfoxide; acetonitrile;