2-(4-((2S)-4-((6-amino-3-pyridinyl)sulfonyl)-2-((1Z)-1-propen-1-yl)-1-piperazinyl)phenyl)-1,1,1,3,3,3-hexafluoro-2-propanol

Base Information

Chemical Name:2-(4-((2S)-4-((6-amino-3-pyridinyl)sulfonyl)-2-((1Z)-1-propen-1-yl)-1-piperazinyl)phenyl)-1,1,1,3,3,3-hexafluoro-2-propanol
CAS No.:1450621-61-0
Molecular Formula:C₂₁H₂₂F₆N₄O₃S
Molecular Weight:524.487
Hs Code.:

Synonyms:2-(4-((2S)-4-((6-amino-3-pyridinyl)sulfonyl)-2-((1Z)-1-propen-1-yl)-1-piperazinyl)phenyl)-1,1,1,3,3,3-hexafluoro-2-propanol

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Chemical Property of 2-(4-((2S)-4-((6-amino-3-pyridinyl)sulfonyl)-2-((1Z)-1-propen-1-yl)-1-piperazinyl)phenyl)-1,1,1,3,3,3-hexafluoro-2-propanol

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Technology Process of 2-(4-((2S)-4-((6-amino-3-pyridinyl)sulfonyl)-2-((1Z)-1-propen-1-yl)-1-piperazinyl)phenyl)-1,1,1,3,3,3-hexafluoro-2-propanol

There total 8 articles about 2-(4-((2S)-4-((6-amino-3-pyridinyl)sulfonyl)-2-((1Z)-1-propen-1-yl)-1-piperazinyl)phenyl)-1,1,1,3,3,3-hexafluoro-2-propanol 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:

: 1361224-53-4
2-(4-((2S)-4-((6-amino-3-pyridinyl)sulphonyl)-2-(1-propyn-1-yl)-1-piperazinyl)phenyl)-1,1,1,3,3,3-hexafluoro-2-propanol

: 1450621-61-0
2-(4-((2S)-4-((6-amino-3-pyridinyl)sulfonyl)-2-((1Z)-1-propen-1-yl)-1-piperazinyl)phenyl)-1,1,1,3,3,3-hexafluoro-2-propanol

Guidance literature:: With quinoline; hydrogen; palladium(II) hydroxide; In ethanol; at 20 ℃; for 1h; Inert atmosphere;

Reference yield:

: 6684-39-5
2-chloropyridine-5-sulfonyl chloride

: 1450621-61-0
2-(4-((2S)-4-((6-amino-3-pyridinyl)sulfonyl)-2-((1Z)-1-propen-1-yl)-1-piperazinyl)phenyl)-1,1,1,3,3,3-hexafluoro-2-propanol

Guidance literature:: Multi-step reaction with 4 steps

1: triethylamine / dichloromethane / 0.17 h / 0 °C

2: ammonium hydroxide / ethanol / 6 h / 110 - 120 °C

3: Chiralpak^? ADH column / methanol / Resolution of racemate

4: quinoline; palladium(II) hydroxide; hydrogen / ethanol / 1 h / 20 °C / Inert atmosphere

With quinoline; ammonium hydroxide; hydrogen; palladium(II) hydroxide; triethylamine; In methanol; ethanol; dichloromethane;

Reference yield:

: 1361224-51-2
benzyl 3-(1-propyn-1-yl)-4-(4-(2,2,2-trifluoro-1-hydroxy-1-(trifluoromethyl)ethyl)-phenyl)-1-piperazinecarboxylate

: 1450621-61-0
2-(4-((2S)-4-((6-amino-3-pyridinyl)sulfonyl)-2-((1Z)-1-propen-1-yl)-1-piperazinyl)phenyl)-1,1,1,3,3,3-hexafluoro-2-propanol

Guidance literature:: Multi-step reaction with 5 steps

1.1: trifluorormethanesulfonic acid; trifluoroacetic acid / 23 °C

1.2: pH 7

2.1: triethylamine / dichloromethane / 0.17 h / 0 °C

3.1: ammonium hydroxide / ethanol / 6 h / 110 - 120 °C

4.1: Chiralpak^? ADH column / methanol / Resolution of racemate

5.1: quinoline; palladium(II) hydroxide; hydrogen / ethanol / 1 h / 20 °C / Inert atmosphere

With quinoline; ammonium hydroxide; trifluorormethanesulfonic acid; hydrogen; palladium(II) hydroxide; triethylamine; trifluoroacetic acid; In methanol; ethanol; dichloromethane;