(S)-4-(1-(1-(5-chloro-3-fluoropyridin-2-yl)piperidin-4-yl)-2-oxopyrrolidin-3-yloxy)-3-fluoro-N-(2-hydroxyethyl)-N-methylbenzamide

Base Information

Chemical Name:(S)-4-(1-(1-(5-chloro-3-fluoropyridin-2-yl)piperidin-4-yl)-2-oxopyrrolidin-3-yloxy)-3-fluoro-N-(2-hydroxyethyl)-N-methylbenzamide
CAS No.:1351167-64-0
Molecular Formula:C₂₄H₂₇ClF₂N₄O₄
Molecular Weight:508.953
Hs Code.:

Synonyms:(S)-4-(1-(1-(5-chloro-3-fluoropyridin-2-yl)piperidin-4-yl)-2-oxopyrrolidin-3-yloxy)-3-fluoro-N-(2-hydroxyethyl)-N-methylbenzamide

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Chemical Property of (S)-4-(1-(1-(5-chloro-3-fluoropyridin-2-yl)piperidin-4-yl)-2-oxopyrrolidin-3-yloxy)-3-fluoro-N-(2-hydroxyethyl)-N-methylbenzamide

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Technology Process of (S)-4-(1-(1-(5-chloro-3-fluoropyridin-2-yl)piperidin-4-yl)-2-oxopyrrolidin-3-yloxy)-3-fluoro-N-(2-hydroxyethyl)-N-methylbenzamide

There total 7 articles about (S)-4-(1-(1-(5-chloro-3-fluoropyridin-2-yl)piperidin-4-yl)-2-oxopyrrolidin-3-yloxy)-3-fluoro-N-(2-hydroxyethyl)-N-methylbenzamide 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: 29.0%

: 109-83-1
(2-hydroxyethyl)(methyl)amine

: 1351168-74-5
(S)-4-(1-(1-(5-chloro-3-fluoropyridin-2-yl)piperidin-4-yl)-2-oxopyrrolidin-3-yloxy)-3-fluorobenzoic acid

: 1351167-64-0
(S)-4-(1-(1-(5-chloro-3-fluoropyridin-2-yl)piperidin-4-yl)-2-oxopyrrolidin-3-yloxy)-3-fluoro-N-(2-hydroxyethyl)-N-methylbenzamide

Guidance literature:: (S)-4-(1-(1-(5-chloro-3-fluoropyridin-2-yl)piperidin-4-yl)-2-oxopyrrolidin-3-yloxy)-3-fluorobenzoic acid; With N-ethyl-N,N-diisopropylamine; HATU; In N,N-dimethyl-formamide; at 20 ℃; for 0.333333h;

(2-hydroxyethyl)(methyl)amine; In N,N-dimethyl-formamide; at 20 ℃; for 2h;

Reference yield:

: 87120-72-7
1-(tert-butoxycarbonyl)-4-aminopiperidine

: 1351167-64-0
(S)-4-(1-(1-(5-chloro-3-fluoropyridin-2-yl)piperidin-4-yl)-2-oxopyrrolidin-3-yloxy)-3-fluoro-N-(2-hydroxyethyl)-N-methylbenzamide

Guidance literature:: Multi-step reaction with 7 steps

1.1: acetic acid / 1,2-dichloro-ethane / 0.25 h / 20 °C

1.2: 20 °C

2.1: triethylamine / tetrahydrofuran / 1 h / 20 °C

3.1: potassium carbonate / N,N-dimethyl-formamide / 60 °C

4.1: hydrogenchloride / ethyl acetate; isopropyl alcohol / 20 °C

5.1: N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide / 60 °C

6.1: water; lithium hydroxide / tetrahydrofuran / 20 °C

7.1: N-ethyl-N,N-diisopropylamine; HATU / N,N-dimethyl-formamide / 0.33 h / 20 °C

7.2: 2 h / 20 °C

With hydrogenchloride; water; potassium carbonate; acetic acid; triethylamine; N-ethyl-N,N-diisopropylamine; HATU; lithium hydroxide; In tetrahydrofuran; ethyl acetate; 1,2-dichloro-ethane; N,N-dimethyl-formamide; isopropyl alcohol;

Reference yield:

: 1351168-43-8
(S)-tert-butyl 4-(3-(2-fluoro-4-(methoxycarbonyl)phenoxy)-2-oxopyrrolidin-1-yl)piperidin-1-carboxylate

: 1351167-64-0
(S)-4-(1-(1-(5-chloro-3-fluoropyridin-2-yl)piperidin-4-yl)-2-oxopyrrolidin-3-yloxy)-3-fluoro-N-(2-hydroxyethyl)-N-methylbenzamide

Guidance literature:: Multi-step reaction with 4 steps

1.1: hydrogenchloride / ethyl acetate; isopropyl alcohol / 20 °C

2.1: N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide / 60 °C

3.1: water; lithium hydroxide / tetrahydrofuran / 20 °C

4.1: N-ethyl-N,N-diisopropylamine; HATU / N,N-dimethyl-formamide / 0.33 h / 20 °C

4.2: 2 h / 20 °C

With hydrogenchloride; water; N-ethyl-N,N-diisopropylamine; HATU; lithium hydroxide; In tetrahydrofuran; ethyl acetate; N,N-dimethyl-formamide; isopropyl alcohol;