(S)-3-(1-(5-ethylpyrimidin-2-yl)piperidin-4-yl)-5-(1-(2-fluoro-4-(methylsulfonyl)phenyl)pyrrolidin-3-yl)-1,2,4-oxadiazole

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Chemical Name:(S)-3-(1-(5-ethylpyrimidin-2-yl)piperidin-4-yl)-5-(1-(2-fluoro-4-(methylsulfonyl)phenyl)pyrrolidin-3-yl)-1,2,4-oxadiazole
CAS No.:1054520-98-7
Molecular Formula:C₂₄H₂₉FN₆O₃S
Molecular Weight:500.597
Hs Code.:

Synonyms:(S)-3-(1-(5-ethylpyrimidin-2-yl)piperidin-4-yl)-5-(1-(2-fluoro-4-(methylsulfonyl)phenyl)pyrrolidin-3-yl)-1,2,4-oxadiazole

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Chemical Property of (S)-3-(1-(5-ethylpyrimidin-2-yl)piperidin-4-yl)-5-(1-(2-fluoro-4-(methylsulfonyl)phenyl)pyrrolidin-3-yl)-1,2,4-oxadiazole

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Technology Process of (S)-3-(1-(5-ethylpyrimidin-2-yl)piperidin-4-yl)-5-(1-(2-fluoro-4-(methylsulfonyl)phenyl)pyrrolidin-3-yl)-1,2,4-oxadiazole

There total 6 articles about (S)-3-(1-(5-ethylpyrimidin-2-yl)piperidin-4-yl)-5-(1-(2-fluoro-4-(methylsulfonyl)phenyl)pyrrolidin-3-yl)-1,2,4-oxadiazole 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:

: 1054521-40-2
(S)-5-(1-(2-fluoro-4-(methylsulfonyl)phenyl)pyrrolidin-3-yl)-3-(piperidin-4-yl)-1,2,4-oxadiazole

: 111196-81-7
2-chloro-5-ethylpyrimidine

: 1054520-98-7
(S)-3-(1-(5-ethylpyrimidin-2-yl)piperidin-4-yl)-5-(1-(2-fluoro-4-(methylsulfonyl)phenyl)pyrrolidin-3-yl)-1,2,4-oxadiazole

Guidance literature:: (S)-5-(1-(2-fluoro-4-(methylsulfonyl)phenyl)pyrrolidin-3-yl)-3-(piperidin-4-yl)-1,2,4-oxadiazole; 2-chloro-5-ethylpyrimidine; With N-ethyl-N,N-diisopropylamine; at 80 ℃; for 0.0833333h;

With copper(l) iodide; at 80 ℃;

Reference yield:

: 424792-57-4
1,2-difluoro-4-(methylsulfonyl)benzene

: 1054520-98-7
(S)-3-(1-(5-ethylpyrimidin-2-yl)piperidin-4-yl)-5-(1-(2-fluoro-4-(methylsulfonyl)phenyl)pyrrolidin-3-yl)-1,2,4-oxadiazole

Guidance literature:: Multi-step reaction with 8 steps

1.1: potassium carbonate / N,N-dimethyl-formamide / 100 °C

2.1: pyridine / dichloromethane

3.1: N,N-dimethyl-formamide / 80 °C

4.1: hydrogenchloride; water / 1 h / Heating / reflux

5.1: 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / N,N-dimethyl-formamide / 20 °C

6.1: 1,4-dioxane / 4 h / 85 °C

7.1: hydrogenchloride / 1,4-dioxane / 2 h

8.1: N-ethyl-N,N-diisopropylamine / 0.08 h / 80 °C

8.2: 80 °C

With pyridine; hydrogenchloride; water; potassium carbonate; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine; In 1,4-dioxane; dichloromethane; N,N-dimethyl-formamide;

Reference yield:

: 1054521-30-0
(R)-1-(2-fluoro-4-(methylsulfonyl)phenyl)pyrrolidin-3-ol

: 1054520-98-7
(S)-3-(1-(5-ethylpyrimidin-2-yl)piperidin-4-yl)-5-(1-(2-fluoro-4-(methylsulfonyl)phenyl)pyrrolidin-3-yl)-1,2,4-oxadiazole

Guidance literature:: Multi-step reaction with 7 steps

1.1: pyridine / dichloromethane

2.1: N,N-dimethyl-formamide / 80 °C

3.1: hydrogenchloride; water / 1 h / Heating / reflux

4.1: 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / N,N-dimethyl-formamide / 20 °C

5.1: 1,4-dioxane / 4 h / 85 °C

6.1: hydrogenchloride / 1,4-dioxane / 2 h

7.1: N-ethyl-N,N-diisopropylamine / 0.08 h / 80 °C

7.2: 80 °C

With pyridine; hydrogenchloride; water; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine; In 1,4-dioxane; dichloromethane; N,N-dimethyl-formamide;