tert-butyl 4-{1-hydroxy-2-[4-(1H-tetrazol-1-yl)phenyl]ethyl}piperidine-1-carboxylate

Base Information

Chemical Name:tert-butyl 4-{1-hydroxy-2-[4-(1H-tetrazol-1-yl)phenyl]ethyl}piperidine-1-carboxylate
CAS No.:1428478-75-4
Molecular Formula:C₁₉H₂₇N₅O₃
Molecular Weight:373.455
Hs Code.:

Synonyms:tert-butyl 4-{1-hydroxy-2-[4-(1H-tetrazol-1-yl)phenyl]ethyl}piperidine-1-carboxylate

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Chemical Property of tert-butyl 4-{1-hydroxy-2-[4-(1H-tetrazol-1-yl)phenyl]ethyl}piperidine-1-carboxylate

Chemical Property:

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Technology Process of tert-butyl 4-{1-hydroxy-2-[4-(1H-tetrazol-1-yl)phenyl]ethyl}piperidine-1-carboxylate

There total 6 articles about tert-butyl 4-{1-hydroxy-2-[4-(1H-tetrazol-1-yl)phenyl]ethyl}piperidine-1-carboxylate 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:

: 1428478-74-3
tert-butyl 4-[2-(4-aminophenyl)-1-hydroxyethyl]piperidine-1-carboxylate

: 122-51-0
orthoformic acid triethyl ester

: 1428478-75-4
tert-butyl 4-{1-hydroxy-2-[4-(1H-tetrazol-1-yl)phenyl]ethyl}piperidine-1-carboxylate

Guidance literature:: With sodium azide; In ethanol; at 60 - 70 ℃; for 1.5h;

Reference yield:

: 139290-70-3
tert-butyl 4-(methoxy(methyl)carbamoyl)piperidine-1-carboxylate

: 1428478-75-4
tert-butyl 4-{1-hydroxy-2-[4-(1H-tetrazol-1-yl)phenyl]ethyl}piperidine-1-carboxylate

Guidance literature:: Multi-step reaction with 5 steps

1: magnesium / tetrahydrofuran; diethyl ether / 2.5 h / 0 °C / Reflux

2: palladium diacetate; caesium carbonate; 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene / 1,4-dioxane / 6 h / Inert atmosphere; Reflux

3: sodium tetrahydroborate / methanol; ethyl acetate / 0.5 h

4: potassium hydroxide / ethanol; water / 24 h / Reflux

5: sodium azide / ethanol / 1.5 h / 60 - 70 °C

With sodium tetrahydroborate; sodium azide; palladium diacetate; caesium carbonate; magnesium; 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene; potassium hydroxide; In tetrahydrofuran; 1,4-dioxane; methanol; diethyl ether; ethanol; water; ethyl acetate;

Reference yield:

: 1428478-71-0
tert-butyl 4-[2-(4-bromophenyl)-1-hydroxyethyl]piperidine-1-carboxylate

: 1428478-75-4
tert-butyl 4-{1-hydroxy-2-[4-(1H-tetrazol-1-yl)phenyl]ethyl}piperidine-1-carboxylate

Guidance literature:: Multi-step reaction with 4 steps

1: palladium diacetate; caesium carbonate; 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene / 1,4-dioxane / 6 h / Inert atmosphere; Reflux

2: sodium tetrahydroborate / methanol; ethyl acetate / 0.5 h

3: potassium hydroxide / ethanol; water / 24 h / Reflux

4: sodium azide / ethanol / 1.5 h / 60 - 70 °C

With sodium tetrahydroborate; sodium azide; palladium diacetate; caesium carbonate; 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene; potassium hydroxide; In 1,4-dioxane; methanol; ethanol; water; ethyl acetate;