1-{4-[2-(2,1,3-benzoxadiazol-5-yl)ethyl]-4-hydroxypiperidin-1-yl}-2-[4-(1H-tetrazol-1-yl)phenyl]ethanone

Base Information

Chemical Name:1-{4-[2-(2,1,3-benzoxadiazol-5-yl)ethyl]-4-hydroxypiperidin-1-yl}-2-[4-(1H-tetrazol-1-yl)phenyl]ethanone
CAS No.:1428477-29-5
Molecular Formula:C₂₂H₂₃N₇O₃
Molecular Weight:433.47
Hs Code.:

Synonyms:1-{4-[2-(2,1,3-benzoxadiazol-5-yl)ethyl]-4-hydroxypiperidin-1-yl}-2-[4-(1H-tetrazol-1-yl)phenyl]ethanone

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Chemical Property of 1-{4-[2-(2,1,3-benzoxadiazol-5-yl)ethyl]-4-hydroxypiperidin-1-yl}-2-[4-(1H-tetrazol-1-yl)phenyl]ethanone

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Technology Process of 1-{4-[2-(2,1,3-benzoxadiazol-5-yl)ethyl]-4-hydroxypiperidin-1-yl}-2-[4-(1H-tetrazol-1-yl)phenyl]ethanone

There total 7 articles about 1-{4-[2-(2,1,3-benzoxadiazol-5-yl)ethyl]-4-hydroxypiperidin-1-yl}-2-[4-(1H-tetrazol-1-yl)phenyl]ethanone 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:

: 1428479-63-3
1-{4-(2,1,3-benzoxadiazol-5-ylethynyl)-4-hydroxypiperidin-1-yl}-2-[4-(1H-tetrazol-1-yl)phenyl]ethanone

: 1428477-29-5
1-{4-[2-(2,1,3-benzoxadiazol-5-yl)ethyl]-4-hydroxypiperidin-1-yl}-2-[4-(1H-tetrazol-1-yl)phenyl]ethanone

Guidance literature:: With palladium on activated charcoal; hydrogen; In ethyl acetate; for 12h; under 760.051 Torr;

Reference yield:

: 185132-51-8
4-hydroxy-4-trimethylsilanylethynylpiperidine-1-carboxylic acid tert-butyl ester

: 1428477-29-5
1-{4-[2-(2,1,3-benzoxadiazol-5-yl)ethyl]-4-hydroxypiperidin-1-yl}-2-[4-(1H-tetrazol-1-yl)phenyl]ethanone

Guidance literature:: Multi-step reaction with 5 steps

1: hydrogenchloride / 1,4-dioxane / 48 h / 20 °C

2: 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine / dichloromethane / 12 h / 5 °C

3: tetrabutyl ammonium fluoride / tetrahydrofuran / 2 h / 5 °C

4: bis-triphenylphosphine-palladium(II) chloride; copper(l) iodide; triethylamine / N,N-dimethyl-formamide / 12 h / 80 °C / Inert atmosphere; Sealed tube

5: palladium on activated charcoal; hydrogen / ethyl acetate / 12 h / 760.05 Torr

With hydrogenchloride; bis-triphenylphosphine-palladium(II) chloride; copper(l) iodide; palladium on activated charcoal; tetrabutyl ammonium fluoride; hydrogen; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; In tetrahydrofuran; 1,4-dioxane; dichloromethane; ethyl acetate; N,N-dimethyl-formamide;

Reference yield:

: 1428478-50-5
1-(4-ethynyl-4-hydroxypiperidin-1-yl)-2-[4-(1H-tetrazol-1-yl)phenyl]ethanone

: 1428477-29-5
1-{4-[2-(2,1,3-benzoxadiazol-5-yl)ethyl]-4-hydroxypiperidin-1-yl}-2-[4-(1H-tetrazol-1-yl)phenyl]ethanone

Guidance literature:: Multi-step reaction with 2 steps

1: bis-triphenylphosphine-palladium(II) chloride; copper(l) iodide; triethylamine / N,N-dimethyl-formamide / 12 h / 80 °C / Inert atmosphere; Sealed tube

2: palladium on activated charcoal; hydrogen / ethyl acetate / 12 h / 760.05 Torr

With bis-triphenylphosphine-palladium(II) chloride; copper(l) iodide; palladium on activated charcoal; hydrogen; triethylamine; In ethyl acetate; N,N-dimethyl-formamide;