N-cyclopropyl-4-oxazol-5-yl-N-[1-(5-phenyl-[1,2,4]oxadiazol-3-yl)piperidin-4-yl]benzamide

Base Information

Chemical Name:N-cyclopropyl-4-oxazol-5-yl-N-[1-(5-phenyl-[1,2,4]oxadiazol-3-yl)piperidin-4-yl]benzamide
CAS No.:1400707-62-1
Molecular Formula:C₂₆H₂₅N₅O₃
Molecular Weight:455.516
Hs Code.:

Synonyms:N-cyclopropyl-4-oxazol-5-yl-N-[1-(5-phenyl-[1,2,4]oxadiazol-3-yl)piperidin-4-yl]benzamide

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Chemical Property of N-cyclopropyl-4-oxazol-5-yl-N-[1-(5-phenyl-[1,2,4]oxadiazol-3-yl)piperidin-4-yl]benzamide

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Technology Process of N-cyclopropyl-4-oxazol-5-yl-N-[1-(5-phenyl-[1,2,4]oxadiazol-3-yl)piperidin-4-yl]benzamide

There total 6 articles about N-cyclopropyl-4-oxazol-5-yl-N-[1-(5-phenyl-[1,2,4]oxadiazol-3-yl)piperidin-4-yl]benzamide 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:

: 1400706-74-2
N-cyclopropyl N-[1-(N-hydroxycarbamimidoyl)piperidin-4-yl]-4-oxazol-5-ylbenzamide

: 98-88-4
benzoyl chloride

: 1400707-62-1
N-cyclopropyl-4-oxazol-5-yl-N-[1-(5-phenyl-[1,2,4]oxadiazol-3-yl)piperidin-4-yl]benzamide

Guidance literature:: With triethylamine; In tetrahydrofuran; at 20 - 80 ℃; for 15.5h;

Reference yield:

: 250161-45-6
4-(1,3-oxazol-5-yl)benzoic acid

: 1400707-62-1
N-cyclopropyl-4-oxazol-5-yl-N-[1-(5-phenyl-[1,2,4]oxadiazol-3-yl)piperidin-4-yl]benzamide

Guidance literature:: Multi-step reaction with 5 steps

1.1: N-ethyl-N,N-diisopropylamine; O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate / N,N-dimethyl-formamide / 0.17 h / 20 °C

1.2: 20 °C

2.1: hydrogenchloride / 1,4-dioxane / 2 h / 20 °C

3.1: N-ethyl-N,N-diisopropylamine / dichloromethane; tetrahydrofuran / 20 °C

4.1: potassium carbonate; hydroxylamine hydrochloride / ethanol; water / 53 h / 20 °C / Reflux

5.1: triethylamine / tetrahydrofuran / 15.5 h / 20 - 80 °C

With hydrogenchloride; hydroxylamine hydrochloride; potassium carbonate; O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate; triethylamine; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; 1,4-dioxane; ethanol; dichloromethane; water; N,N-dimethyl-formamide;

Reference yield:

: 1400706-57-1
(N-cyclopropyl)-4-oxazol-5-yl-(N-piperidin-4-yl)benzamide

: 1400707-62-1
N-cyclopropyl-4-oxazol-5-yl-N-[1-(5-phenyl-[1,2,4]oxadiazol-3-yl)piperidin-4-yl]benzamide

Guidance literature:: Multi-step reaction with 3 steps

1: N-ethyl-N,N-diisopropylamine / dichloromethane; tetrahydrofuran / 20 °C

2: potassium carbonate; hydroxylamine hydrochloride / ethanol; water / 53 h / 20 °C / Reflux

3: triethylamine / tetrahydrofuran / 15.5 h / 20 - 80 °C

With hydroxylamine hydrochloride; potassium carbonate; triethylamine; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; ethanol; dichloromethane; water;