2-(4-((2S)-4-((6-amino-3-pyridazinyl)sulfonyl)-2-(1-propyn-1-yl)-1-piperazinyl)phenyl)-1,1,1,3,3,3-hexafluoro-2-propanol

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Chemical Name:2-(4-((2S)-4-((6-amino-3-pyridazinyl)sulfonyl)-2-(1-propyn-1-yl)-1-piperazinyl)phenyl)-1,1,1,3,3,3-hexafluoro-2-propanol
CAS No.:1450620-95-7
Molecular Formula:C₂₀H₁₉F₆N₅O₃S
Molecular Weight:523.459
Hs Code.:

Synonyms:2-(4-((2S)-4-((6-amino-3-pyridazinyl)sulfonyl)-2-(1-propyn-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-pyridazinyl)sulfonyl)-2-(1-propyn-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-pyridazinyl)sulfonyl)-2-(1-propyn-1-yl)-1-piperazinyl)phenyl)-1,1,1,3,3,3-hexafluoro-2-propanol

There total 13 articles about 2-(4-((2S)-4-((6-amino-3-pyridazinyl)sulfonyl)-2-(1-propyn-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:

: 1450620-96-8
2-(4-((2S)-4-((6-chloro-3-pyridazinyl)sulfonyl)-2-(1-propyn-1-yl)-1-piperazinyl)phenyl)-1,1,1,3,3,3-hexafluoro-2-propanol

: 1450620-95-7
2-(4-((2S)-4-((6-amino-3-pyridazinyl)sulfonyl)-2-(1-propyn-1-yl)-1-piperazinyl)phenyl)-1,1,1,3,3,3-hexafluoro-2-propanol

Guidance literature:: With ammonium hydroxide; In ethanol; at 100 ℃; for 1h; Microwave irradiation;

Reference yield:

: 1450620-14-0
4-benzyl 1-tert-butyl 2-(1-propyn-1-yl)-1,4-piperazinedicarboxylate

: 1450620-95-7
2-(4-((2S)-4-((6-amino-3-pyridazinyl)sulfonyl)-2-(1-propyn-1-yl)-1-piperazinyl)phenyl)-1,1,1,3,3,3-hexafluoro-2-propanol

Guidance literature:: Multi-step reaction with 6 steps

1: Chiralpak^? ADH column / ethanol / Resolution of racemate

2: trifluoroacetic acid / dichloromethane / 0.67 h / 20 °C

3: ruphos; chloro-(2-dicyclohexylphosphino-2’,6’-diisopropoxy-1,1‘-biphenyl)[2-(2-aminoethyl)phenyl] palladium(ll) methyl-tert-butyl ether adduct / toluene / 2.33 h / 100 °C / Inert atmosphere

4: trifluorormethanesulfonic acid; trifluoroacetic acid / 0.17 h

5: triethylamine / dichloromethane / 0.08 h / 20 °C

6: ammonium hydroxide / ethanol / 1 h / 100 °C / Microwave irradiation

With ammonium hydroxide; trifluorormethanesulfonic acid; chloro-(2-dicyclohexylphosphino-2’,6’-diisopropoxy-1,1‘-biphenyl)[2-(2-aminoethyl)phenyl] palladium(ll) methyl-tert-butyl ether adduct; triethylamine; trifluoroacetic acid; ruphos; In ethanol; dichloromethane; toluene;

Reference yield:

: 1450621-77-8
ethyl 2-[benzyl-[(2S)-2-(tert-butoxycarbonylamino)pent-4-ynoyl]amino]acetate

: 1450620-95-7
2-(4-((2S)-4-((6-amino-3-pyridazinyl)sulfonyl)-2-(1-propyn-1-yl)-1-piperazinyl)phenyl)-1,1,1,3,3,3-hexafluoro-2-propanol

Guidance literature:: Multi-step reaction with 7 steps

1.1: trifluoroacetic acid / dichloromethane / 0.5 h / 20 °C

1.2: 0.17 h / 20 °C

2.1: lithium aluminium tetrahydride / tetrahydrofuran / 12 h / 65 °C

3.1: potassium tert-butylate / tetrahydrofuran / 0.5 h / 20 °C

4.1: ruphos; chloro-(2-dicyclohexylphosphino-2’,6’-diisopropoxy-1,1‘-biphenyl)[2-(2-aminoethyl)phenyl] palladium(ll) methyl-tert-butyl ether adduct; sodium t-butanolate / 1,4-dioxane / 12 h / 80 °C

5.1: carbonochloridic acid 1-chloro-ethyl ester; potassium carbonate / dichloromethane / 0.5 h / 20 °C

6.1: triethylamine / dichloromethane / 0.08 h / 20 °C

7.1: ammonium hydroxide / ethanol / 1 h / 100 °C / Microwave irradiation

With ammonium hydroxide; lithium aluminium tetrahydride; carbonochloridic acid 1-chloro-ethyl ester; chloro-(2-dicyclohexylphosphino-2’,6’-diisopropoxy-1,1‘-biphenyl)[2-(2-aminoethyl)phenyl] palladium(ll) methyl-tert-butyl ether adduct; potassium tert-butylate; potassium carbonate; triethylamine; trifluoroacetic acid; sodium t-butanolate; ruphos; In tetrahydrofuran; 1,4-dioxane; ethanol; dichloromethane;