(R)-5-(1H-indol-4-yl)-3-(4-(tetrahydrofuran-3-yloxy)-3-(trifluoromethyl)phenyl)-1,2,4-oxadiazole

Base Information

Chemical Name:(R)-5-(1H-indol-4-yl)-3-(4-(tetrahydrofuran-3-yloxy)-3-(trifluoromethyl)phenyl)-1,2,4-oxadiazole
CAS No.:1311258-44-2
Molecular Formula:C₂₁H₁₆F₃N₃O₃
Molecular Weight:415.372
Hs Code.:

Synonyms:(R)-5-(1H-indol-4-yl)-3-(4-(tetrahydrofuran-3-yloxy)-3-(trifluoromethyl)phenyl)-1,2,4-oxadiazole

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Chemical Property of (R)-5-(1H-indol-4-yl)-3-(4-(tetrahydrofuran-3-yloxy)-3-(trifluoromethyl)phenyl)-1,2,4-oxadiazole

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Technology Process of (R)-5-(1H-indol-4-yl)-3-(4-(tetrahydrofuran-3-yloxy)-3-(trifluoromethyl)phenyl)-1,2,4-oxadiazole

There total 4 articles about (R)-5-(1H-indol-4-yl)-3-(4-(tetrahydrofuran-3-yloxy)-3-(trifluoromethyl)phenyl)-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:

: 2124-55-2
1H-indole-4-carboxylic acid

: 1311255-49-8
(R)-N'-hydroxy-4-(tetrahydrofuran-3-yloxy)-3-(trifluoromethyl)benzimidamide

: 1311258-44-2
(R)-5-(1H-indol-4-yl)-3-(4-(tetrahydrofuran-3-yloxy)-3-(trifluoromethyl)phenyl)-1,2,4-oxadiazole

Guidance literature:: 1H-indole-4-carboxylic acid; With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In N,N-dimethyl-formamide; at 20 ℃; for 1h; Inert atmosphere;

(R)-N'-hydroxy-4-(tetrahydrofuran-3-yloxy)-3-(trifluoromethyl)benzimidamide; In N,N-dimethyl-formamide; at 140 ℃; for 2h;

Reference yield:

: 124811-71-8
4-hydroxy-3-(trifluoromethyl)benzonitrile

: 1311258-44-2
(R)-5-(1H-indol-4-yl)-3-(4-(tetrahydrofuran-3-yloxy)-3-(trifluoromethyl)phenyl)-1,2,4-oxadiazole

Guidance literature:: Multi-step reaction with 3 steps

1.1: triphenylphosphine; di-isopropyl azodicarboxylate / tetrahydrofuran / 0.17 h / 0 °C / Inert atmosphere

1.2: 0 - 20 °C / Inert atmosphere

2.1: hydroxylamine / ethanol; water / 18 h / 60 °C

3.1: 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; benzotriazol-1-ol / N,N-dimethyl-formamide / 1 h / 20 °C / Inert atmosphere

3.2: 2 h / 140 °C

With di-isopropyl azodicarboxylate; hydroxylamine; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triphenylphosphine; In tetrahydrofuran; ethanol; water; N,N-dimethyl-formamide;

Reference yield:

: 1311255-47-6
(R)-4-(tetrahydrofuran-3-yloxy)-3-(trifluoromethyl)benzonitrile

: 1311258-44-2
(R)-5-(1H-indol-4-yl)-3-(4-(tetrahydrofuran-3-yloxy)-3-(trifluoromethyl)phenyl)-1,2,4-oxadiazole

Guidance literature:: Multi-step reaction with 2 steps

1.1: hydroxylamine / ethanol; water / 18 h / 60 °C

2.1: 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; benzotriazol-1-ol / N,N-dimethyl-formamide / 1 h / 20 °C / Inert atmosphere

2.2: 2 h / 140 °C

With hydroxylamine; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In ethanol; water; N,N-dimethyl-formamide;