N-cyclopropyl N-[1-(N-hydroxycarbamimidoyl)piperidin-4-yl]-4-oxazol-5-ylbenzamide

Base Information

Chemical Name:N-cyclopropyl N-[1-(N-hydroxycarbamimidoyl)piperidin-4-yl]-4-oxazol-5-ylbenzamide
CAS No.:1400706-74-2
Molecular Formula:C₁₉H₂₃N₅O₃
Molecular Weight:369.423
Hs Code.:

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

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Chemical Property of N-cyclopropyl N-[1-(N-hydroxycarbamimidoyl)piperidin-4-yl]-4-oxazol-5-ylbenzamide

Chemical Property:

Purity/Quality:

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Technology Process of N-cyclopropyl N-[1-(N-hydroxycarbamimidoyl)piperidin-4-yl]-4-oxazol-5-ylbenzamide

There total 5 articles about N-cyclopropyl N-[1-(N-hydroxycarbamimidoyl)piperidin-4-yl]-4-oxazol-5-ylbenzamide 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:

: 1400706-58-2
N-(1-cyanopiperidin-4-yl)-N-cyclopropyl-4-oxazol-5-ylbenzamide

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

Guidance literature:: With hydroxylamine hydrochloride; potassium carbonate; In ethanol; water; at 20 ℃; for 53h; Reflux;

Reference yield:

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

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

Guidance literature:: Multi-step reaction with 4 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

With hydrogenchloride; hydroxylamine hydrochloride; potassium carbonate; O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate; 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

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

Guidance literature:: Multi-step reaction with 2 steps

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

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

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