4-(diphenylhydroxymethyl)-3-isopropoxy-5-(1-methoxycarbonyl-4-piperidyl)isoxazole

Base Information

Chemical Name:4-(diphenylhydroxymethyl)-3-isopropoxy-5-(1-methoxycarbonyl-4-piperidyl)isoxazole
CAS No.:439944-74-8
Molecular Formula:C₂₆H₃₀N₂O₅
Molecular Weight:450.535
Hs Code.:

Synonyms:4-(diphenylhydroxymethyl)-3-isopropoxy-5-(1-methoxycarbonyl-4-piperidyl)isoxazole

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Chemical Property of 4-(diphenylhydroxymethyl)-3-isopropoxy-5-(1-methoxycarbonyl-4-piperidyl)isoxazole

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Technology Process of 4-(diphenylhydroxymethyl)-3-isopropoxy-5-(1-methoxycarbonyl-4-piperidyl)isoxazole

There total 1 articles about 4-(diphenylhydroxymethyl)-3-isopropoxy-5-(1-methoxycarbonyl-4-piperidyl)isoxazole 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: 63.0%

: 119-61-9
benzophenone

: 439944-76-0
4-iodo-3-isopropoxy-5-(1-methoxycarbonyl-4-piperidyl)isoxazole

: 439944-74-8
4-(diphenylhydroxymethyl)-3-isopropoxy-5-(1-methoxycarbonyl-4-piperidyl)isoxazole

Guidance literature:: 4-iodo-3-isopropoxy-5-(1-methoxycarbonyl-4-piperidyl)isoxazole; With ethylmagnesium chloride; In tetrahydrofuran; at 0 ℃; for 1h;

benzophenone; In tetrahydrofuran; at 20 ℃; for 18h; Further stages.;
DOI:10.1021/jm020027o

Reference yield: 78.0%

: 439944-74-8
4-(diphenylhydroxymethyl)-3-isopropoxy-5-(1-methoxycarbonyl-4-piperidyl)isoxazole

: 439944-78-2
4-(diphenylmethyl)-3-isopropoxy-5-(1-methoxycarbonyl-4-piperidyl)isoxazole

Guidance literature:: With triethylsilane; trifluoroacetic acid; In dichloromethane; at 0 ℃;
DOI:10.1021/jm020027o

Reference yield:

: 439944-74-8
4-(diphenylhydroxymethyl)-3-isopropoxy-5-(1-methoxycarbonyl-4-piperidyl)isoxazole

: 4-benzhydryl-5-piperidin-4-yl-isoxazol-3-ol; hydrobromide

Guidance literature:: Multi-step reaction with 2 steps

1: 78 percent / Et₃SiH; TFA / CH₂Cl₂ / 0 °C

2: 24 percent / HBr; AcOH / 18 h / 65 °C

With triethylsilane; hydrogen bromide; acetic acid; trifluoroacetic acid; In dichloromethane;
DOI:10.1021/jm020027o