5-methyl-3-(1-(3-(trifluoromethyl)phenyl)-1H-indol-3-yl)-4,5-dihydroisoxazole-5-carboxylic acid

Base Information

Chemical Name:5-methyl-3-(1-(3-(trifluoromethyl)phenyl)-1H-indol-3-yl)-4,5-dihydroisoxazole-5-carboxylic acid
CAS No.:1283629-16-2
Molecular Formula:C₂₀H₁₅F₃N₂O₃
Molecular Weight:388.346
Hs Code.:

Synonyms:5-methyl-3-(1-(3-(trifluoromethyl)phenyl)-1H-indol-3-yl)-4,5-dihydroisoxazole-5-carboxylic acid

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Chemical Property of 5-methyl-3-(1-(3-(trifluoromethyl)phenyl)-1H-indol-3-yl)-4,5-dihydroisoxazole-5-carboxylic acid

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Technology Process of 5-methyl-3-(1-(3-(trifluoromethyl)phenyl)-1H-indol-3-yl)-4,5-dihydroisoxazole-5-carboxylic acid

There total 6 articles about 5-methyl-3-(1-(3-(trifluoromethyl)phenyl)-1H-indol-3-yl)-4,5-dihydroisoxazole-5-carboxylic 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: 78.0%

: 1283629-14-0
5-methyl-3-(1-(3-(trifluoromethyl)phenyl)-1H-indol-3-yl)-5-(1-methoxy-1-oxomethyl)-4,5-dihydroisoxazole

: 1283629-16-2
5-methyl-3-(1-(3-(trifluoromethyl)phenyl)-1H-indol-3-yl)-4,5-dihydroisoxazole-5-carboxylic acid

Guidance literature:: With lithium hydroxide monohydrate; In tetrahydrofuran; methanol; water; at 20 ℃; for 3h;
DOI:10.1016/j.bmcl.2010.12.127

Reference yield:

: 120-72-9
indole

: 1283629-16-2
5-methyl-3-(1-(3-(trifluoromethyl)phenyl)-1H-indol-3-yl)-4,5-dihydroisoxazole-5-carboxylic acid

Guidance literature:: Multi-step reaction with 5 steps

1.1: copper(l) iodide; caesium carbonate / N,N-dimethyl-formamide / 3 h / 165 °C

2.1: trichlorophosphate / 0.25 h / 0 °C / Inert atmosphere

2.2: 2 h / 164 °C / Inert atmosphere

3.1: hydroxylamine hydrochloride / pyridine; ethanol / 16 h / 20 °C / Inert atmosphere

4.1: sodium hypochlorite / tetrahydrofuran / 16 h / 20 °C / Inert atmosphere

5.1: lithium hydroxide monohydrate / tetrahydrofuran; methanol; water / 3 h / 20 °C

With sodium hypochlorite; copper(l) iodide; lithium hydroxide monohydrate; hydroxylamine hydrochloride; caesium carbonate; trichlorophosphate; In tetrahydrofuran; pyridine; methanol; ethanol; water; N,N-dimethyl-formamide;
DOI:10.1016/j.bmcl.2010.12.127

Reference yield:

: 1-(3-(trifluoromethyl)phenyl)-1H-indole

: 1283629-16-2
5-methyl-3-(1-(3-(trifluoromethyl)phenyl)-1H-indol-3-yl)-4,5-dihydroisoxazole-5-carboxylic acid

Guidance literature:: Multi-step reaction with 4 steps

1.1: trichlorophosphate / 0.25 h / 0 °C / Inert atmosphere

1.2: 2 h / 164 °C / Inert atmosphere

2.1: hydroxylamine hydrochloride / pyridine; ethanol / 16 h / 20 °C / Inert atmosphere

3.1: sodium hypochlorite / tetrahydrofuran / 16 h / 20 °C / Inert atmosphere

4.1: lithium hydroxide monohydrate / tetrahydrofuran; methanol; water / 3 h / 20 °C

With sodium hypochlorite; lithium hydroxide monohydrate; hydroxylamine hydrochloride; trichlorophosphate; In tetrahydrofuran; pyridine; methanol; ethanol; water;
DOI:10.1016/j.bmcl.2010.12.127