3-[5-(5-{3-cyano-4-[(2,2,2-trifluoroethyl)oxy]phenyl}-1,2,4-oxadiazol-3-yl)-1-isoquinolinyl]propanoic acid

Base Information

Chemical Name:3-[5-(5-{3-cyano-4-[(2,2,2-trifluoroethyl)oxy]phenyl}-1,2,4-oxadiazol-3-yl)-1-isoquinolinyl]propanoic acid
CAS No.:1192829-57-4
Molecular Formula:C₂₃H₁₅F₃N₄O₄
Molecular Weight:468.392
Hs Code.:

Synonyms:3-[5-(5-{3-cyano-4-[(2,2,2-trifluoroethyl)oxy]phenyl}-1,2,4-oxadiazol-3-yl)-1-isoquinolinyl]propanoic acid

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Chemical Property of 3-[5-(5-{3-cyano-4-[(2,2,2-trifluoroethyl)oxy]phenyl}-1,2,4-oxadiazol-3-yl)-1-isoquinolinyl]propanoic acid

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Technology Process of 3-[5-(5-{3-cyano-4-[(2,2,2-trifluoroethyl)oxy]phenyl}-1,2,4-oxadiazol-3-yl)-1-isoquinolinyl]propanoic acid

There total 7 articles about 3-[5-(5-{3-cyano-4-[(2,2,2-trifluoroethyl)oxy]phenyl}-1,2,4-oxadiazol-3-yl)-1-isoquinolinyl]propanoic acid 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:

: 1192829-99-4
1,1-dimethylethyl 3-[5-(5-{3-cyano-4-[(2,2,2-trifluoroethyl)oxy]phenyl}-1,2,4-oxadiazol-3-yl)-1-isoquinolinyl]propanoate

: 1192829-57-4
3-[5-(5-{3-cyano-4-[(2,2,2-trifluoroethyl)oxy]phenyl}-1,2,4-oxadiazol-3-yl)-1-isoquinolinyl]propanoic acid

Guidance literature:: With hydrogenchloride; In 1,4-dioxane; at 20 ℃; for 2.5h;

Reference yield:

: 34784-04-8
5-bromoisoquinoline

: 1192829-57-4
3-[5-(5-{3-cyano-4-[(2,2,2-trifluoroethyl)oxy]phenyl}-1,2,4-oxadiazol-3-yl)-1-isoquinolinyl]propanoic acid

Guidance literature:: Multi-step reaction with 6 steps

1.1: aluminum (III) chloride / dichloromethane / 3.08 h / 30 °C

2.1: sodium hydride / N,N-dimethyl-formamide / 3.83 h / -10 - 20 °C / Inert atmosphere

3.1: 1,1'-bis-(diphenylphosphino)ferrocene; sodium carbonate; potassium hexacyanoferrate(III) / palladium diacetate / DMA / 120 °C

4.1: hydroxylamine hydrochloride; sodium hydrogencarbonate / ethanol / 5 h / 60 °C

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

5.2: 0.5 h / 120 °C / Microwave

6.1: hydrogenchloride / 1,4-dioxane / 2.5 h / 20 °C

With hydrogenchloride; 1,1'-bis-(diphenylphosphino)ferrocene; hydroxylamine hydrochloride; sodium hydride; sodium hydrogencarbonate; sodium carbonate; N-ethyl-N,N-diisopropylamine; HATU; potassium hexacyanoferrate(III); aluminum (III) chloride; palladium diacetate; In 1,4-dioxane; DMA; ethanol; dichloromethane; N,N-dimethyl-formamide;

Reference yield:

: 1192829-83-6
1,1-dimethylethyl 3-(5-bromo-1-isoquinolinyl)propanoate

: 1192829-57-4
3-[5-(5-{3-cyano-4-[(2,2,2-trifluoroethyl)oxy]phenyl}-1,2,4-oxadiazol-3-yl)-1-isoquinolinyl]propanoic acid

Guidance literature:: Multi-step reaction with 4 steps

1.1: 1,1'-bis-(diphenylphosphino)ferrocene; sodium carbonate; potassium hexacyanoferrate(III) / palladium diacetate / DMA / 120 °C

2.1: hydroxylamine hydrochloride; sodium hydrogencarbonate / ethanol / 5 h / 60 °C

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

3.2: 0.5 h / 120 °C / Microwave

4.1: hydrogenchloride / 1,4-dioxane / 2.5 h / 20 °C

With hydrogenchloride; 1,1'-bis-(diphenylphosphino)ferrocene; hydroxylamine hydrochloride; sodium hydrogencarbonate; sodium carbonate; N-ethyl-N,N-diisopropylamine; HATU; potassium hexacyanoferrate(III); palladium diacetate; In 1,4-dioxane; DMA; ethanol; N,N-dimethyl-formamide;