(3S)-ethyl 1-(2-hydroxy-2-(4-(5-(3-(pyridin-2-yl)-4-(trifluoromethyl)isoxazol-5-yl)-1,2,4-oxadiazol-3-yl)phenyl)ethyl)piperidine-3-carboxylate

Base Information

Chemical Name:(3S)-ethyl 1-(2-hydroxy-2-(4-(5-(3-(pyridin-2-yl)-4-(trifluoromethyl)isoxazol-5-yl)-1,2,4-oxadiazol-3-yl)phenyl)ethyl)piperidine-3-carboxylate
CAS No.:1265323-54-3
Molecular Formula:C₂₇H₂₆F₃N₅O₅
Molecular Weight:557.529
Hs Code.:

Synonyms:(3S)-ethyl 1-(2-hydroxy-2-(4-(5-(3-(pyridin-2-yl)-4-(trifluoromethyl)isoxazol-5-yl)-1,2,4-oxadiazol-3-yl)phenyl)ethyl)piperidine-3-carboxylate

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Chemical Property of (3S)-ethyl 1-(2-hydroxy-2-(4-(5-(3-(pyridin-2-yl)-4-(trifluoromethyl)isoxazol-5-yl)-1,2,4-oxadiazol-3-yl)phenyl)ethyl)piperidine-3-carboxylate

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Technology Process of (3S)-ethyl 1-(2-hydroxy-2-(4-(5-(3-(pyridin-2-yl)-4-(trifluoromethyl)isoxazol-5-yl)-1,2,4-oxadiazol-3-yl)phenyl)ethyl)piperidine-3-carboxylate

There total 4 articles about (3S)-ethyl 1-(2-hydroxy-2-(4-(5-(3-(pyridin-2-yl)-4-(trifluoromethyl)isoxazol-5-yl)-1,2,4-oxadiazol-3-yl)phenyl)ethyl)piperidine-3-carboxylate 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:

: 1236144-58-3
3-(pyridin-2-yl)-4-(trifluoromethyl)isoxazole-5-carboxylic acid

: 1265750-15-9
(3S)-ethyl 1-(2-hydroxy-2-(4-((E)-N'-hydroxycarbamimidoyl)phenyl)ethyl)piperidine-3-carboxylate

: 1265323-54-3
(3S)-ethyl 1-(2-hydroxy-2-(4-(5-(3-(pyridin-2-yl)-4-(trifluoromethyl)isoxazol-5-yl)-1,2,4-oxadiazol-3-yl)phenyl)ethyl)piperidine-3-carboxylate

Guidance literature:: 3-(pyridin-2-yl)-4-(trifluoromethyl)isoxazole-5-carboxylic acid; (3S)-ethyl 1-(2-hydroxy-2-(4-((E)-N'-hydroxycarbamimidoyl)phenyl)ethyl)piperidine-3-carboxylate; With bis-(2-oxo-3-oxazolidinyl)phosphoryl chloride; triethylamine; In N,N-dimethyl-formamide; at 20 ℃; for 2h;

With tetrabutyl ammonium fluoride; In N,N-dimethyl-formamide; for 72h;

Reference yield:

: 1193-96-0
(E)-pyridin-2-aldoxime

: 1265323-54-3
(3S)-ethyl 1-(2-hydroxy-2-(4-(5-(3-(pyridin-2-yl)-4-(trifluoromethyl)isoxazol-5-yl)-1,2,4-oxadiazol-3-yl)phenyl)ethyl)piperidine-3-carboxylate

Guidance literature:: Multi-step reaction with 4 steps

1.1: N-chloro-succinimide / N,N-dimethyl-formamide / 20 - 60 °C

2.1: indium(III) chloride / ethyl acetate / 0.5 h / Inert atmosphere

2.2: 14 h

3.1: water; lithium hydroxide monohydrate / methanol / 1 h / 20 °C

4.1: bis-(2-oxo-3-oxazolidinyl)phosphoryl chloride; triethylamine / N,N-dimethyl-formamide / 2 h / 20 °C

4.2: 72 h

With indium(III) chloride; N-chloro-succinimide; lithium hydroxide monohydrate; water; bis-(2-oxo-3-oxazolidinyl)phosphoryl chloride; triethylamine; In methanol; ethyl acetate; N,N-dimethyl-formamide;

Reference yield:

: 69716-28-5
2-pyridylhydroxyiminomethyl chloride

: 1265323-54-3
(3S)-ethyl 1-(2-hydroxy-2-(4-(5-(3-(pyridin-2-yl)-4-(trifluoromethyl)isoxazol-5-yl)-1,2,4-oxadiazol-3-yl)phenyl)ethyl)piperidine-3-carboxylate

Guidance literature:: Multi-step reaction with 3 steps

1.1: indium(III) chloride / ethyl acetate / 0.5 h / Inert atmosphere

1.2: 14 h

2.1: water; lithium hydroxide monohydrate / methanol / 1 h / 20 °C

3.1: bis-(2-oxo-3-oxazolidinyl)phosphoryl chloride; triethylamine / N,N-dimethyl-formamide / 2 h / 20 °C

3.2: 72 h

With indium(III) chloride; lithium hydroxide monohydrate; water; bis-(2-oxo-3-oxazolidinyl)phosphoryl chloride; triethylamine; In methanol; ethyl acetate; N,N-dimethyl-formamide;