2-(4-(5-(4-isopropoxy-3-(trifluoromethyl)phenyl)-1,2,4-oxadiazol-3-yl)-2,3-dihydro-1H-inden-1-ylamino)ethanol

Base Information

Chemical Name:2-(4-(5-(4-isopropoxy-3-(trifluoromethyl)phenyl)-1,2,4-oxadiazol-3-yl)-2,3-dihydro-1H-inden-1-ylamino)ethanol
CAS No.:1201447-09-7
Molecular Formula:C₂₃H₂₄F₃N₃O₃
Molecular Weight:447.457
Hs Code.:

Synonyms:2-(4-(5-(4-isopropoxy-3-(trifluoromethyl)phenyl)-1,2,4-oxadiazol-3-yl)-2,3-dihydro-1H-inden-1-ylamino)ethanol

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Chemical Property of 2-(4-(5-(4-isopropoxy-3-(trifluoromethyl)phenyl)-1,2,4-oxadiazol-3-yl)-2,3-dihydro-1H-inden-1-ylamino)ethanol

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Technology Process of 2-(4-(5-(4-isopropoxy-3-(trifluoromethyl)phenyl)-1,2,4-oxadiazol-3-yl)-2,3-dihydro-1H-inden-1-ylamino)ethanol

There total 4 articles about 2-(4-(5-(4-isopropoxy-3-(trifluoromethyl)phenyl)-1,2,4-oxadiazol-3-yl)-2,3-dihydro-1H-inden-1-ylamino)ethanol 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: 40.0%

: 1201447-01-9
4-(5-(4-isopropoxy-3-(trifluoromethyl)phenyl)-1,2,4-oxadiazol-3-yl)-2,3-dihydro-1H-inden-1-ol

: 141-43-5
ethanolamine

: 1201447-09-7
2-(4-(5-(4-isopropoxy-3-(trifluoromethyl)phenyl)-1,2,4-oxadiazol-3-yl)-2,3-dihydro-1H-inden-1-ylamino)ethanol

Guidance literature:: 4-(5-(4-isopropoxy-3-(trifluoromethyl)phenyl)-1,2,4-oxadiazol-3-yl)-2,3-dihydro-1H-inden-1-ol; With pyridine; thionyl chloride; In dichloromethane; at 0 - 20 ℃;

ethanolamine; With N-ethyl-N,N-diisopropylamine; In N,N-dimethyl-formamide; at 0 - 60 ℃;

Reference yield:

: 60899-34-5
4-cyano-2,3-dihydro-1H-inden-1-one

: 1201447-09-7
2-(4-(5-(4-isopropoxy-3-(trifluoromethyl)phenyl)-1,2,4-oxadiazol-3-yl)-2,3-dihydro-1H-inden-1-ylamino)ethanol

Guidance literature:: Multi-step reaction with 4 steps

1.1: sodium tetrahydroborate; ethanol; silica gel / 0 - 20 °C

2.1: hydroxylamine hydrochloride; potassium carbonate / ethanol / 16 h / Reflux

3.1: benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / N,N-dimethyl-formamide / 0.33 h / 20 °C

3.2: 1.08 h / 20 - 130 °C / Microwave irradiation

4.1: pyridine; thionyl chloride / dichloromethane / 0 - 20 °C

4.2: 0 - 60 °C

With pyridine; sodium tetrahydroborate; thionyl chloride; ethanol; hydroxylamine hydrochloride; silica gel; potassium carbonate; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In ethanol; dichloromethane; N,N-dimethyl-formamide;

Reference yield:

: 125114-76-3,1306763-24-5
(±)-1-hydroxy-2,3-dihydro-1H-indene-4-carbonitrile

: 1201447-09-7
2-(4-(5-(4-isopropoxy-3-(trifluoromethyl)phenyl)-1,2,4-oxadiazol-3-yl)-2,3-dihydro-1H-inden-1-ylamino)ethanol

Guidance literature:: Multi-step reaction with 3 steps

1.1: hydroxylamine hydrochloride; potassium carbonate / ethanol / 16 h / Reflux

2.1: benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / N,N-dimethyl-formamide / 0.33 h / 20 °C

2.2: 1.08 h / 20 - 130 °C / Microwave irradiation

3.1: pyridine; thionyl chloride / dichloromethane / 0 - 20 °C

3.2: 0 - 60 °C

With pyridine; thionyl chloride; hydroxylamine hydrochloride; potassium carbonate; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In ethanol; dichloromethane; N,N-dimethyl-formamide;