(S)-N-(6,7-dihydro-2-nitro-5H-imidazo [2,1-b][1,3]oxazin-6-yl)-2-(4-(4-(trifluoromethoxy)phenoxy)piperidin-1-yl)acetamide

Base Information

Chemical Name:(S)-N-(6,7-dihydro-2-nitro-5H-imidazo [2,1-b][1,3]oxazin-6-yl)-2-(4-(4-(trifluoromethoxy)phenoxy)piperidin-1-yl)acetamide
CAS No.:1346017-36-4
Molecular Formula:C₂₀H₂₂F₃N₅O₆
Molecular Weight:485.42
Hs Code.:

Synonyms:(S)-N-(6,7-dihydro-2-nitro-5H-imidazo [2,1-b][1,3]oxazin-6-yl)-2-(4-(4-(trifluoromethoxy)phenoxy)piperidin-1-yl)acetamide

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Chemical Property of (S)-N-(6,7-dihydro-2-nitro-5H-imidazo [2,1-b][1,3]oxazin-6-yl)-2-(4-(4-(trifluoromethoxy)phenoxy)piperidin-1-yl)acetamide

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Technology Process of (S)-N-(6,7-dihydro-2-nitro-5H-imidazo [2,1-b][1,3]oxazin-6-yl)-2-(4-(4-(trifluoromethoxy)phenoxy)piperidin-1-yl)acetamide

There total 7 articles about (S)-N-(6,7-dihydro-2-nitro-5H-imidazo [2,1-b][1,3]oxazin-6-yl)-2-(4-(4-(trifluoromethoxy)phenoxy)piperidin-1-yl)acetamide 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: 42.0%

: 1346017-99-9
(S)-2-chloro-N-(2-nitro-6,7-dihydro-5H-imidazo[2,1-b][1,3]oxazin-6-yl) acetamide

: 287952-67-4
4-(4-(trifluoromethoxy)phenoxy)piperidine

: 1346017-36-4
(S)-N-(6,7-dihydro-2-nitro-5H-imidazo [2,1-b][1,3]oxazin-6-yl)-2-(4-(4-(trifluoromethoxy)phenoxy)piperidin-1-yl)acetamide

Guidance literature:: With potassium carbonate; In N,N-dimethyl-formamide; at 50 ℃; Inert atmosphere;

Reference yield:

: 50824-05-0
4-trifluoromethoxybenzyl bromide

: 1346017-36-4
(S)-N-(6,7-dihydro-2-nitro-5H-imidazo [2,1-b][1,3]oxazin-6-yl)-2-(4-(4-(trifluoromethoxy)phenoxy)piperidin-1-yl)acetamide

Guidance literature:: Multi-step reaction with 3 steps

1.1: sodium hydride / N,N-dimethyl-formamide; mineral oil / 0.5 h / Cooling with ice

1.2: 15 h / 20 °C

2.1: hydrogenchloride / 1,4-dioxane / 3 h / 20 °C

3.1: potassium carbonate / N,N-dimethyl-formamide / 50 °C / Inert atmosphere

With hydrogenchloride; sodium hydride; potassium carbonate; In 1,4-dioxane; N,N-dimethyl-formamide; mineral oil;

Reference yield:

: 828-27-3
4-Trifluoromethoxyphenol

: 1346017-36-4
(S)-N-(6,7-dihydro-2-nitro-5H-imidazo [2,1-b][1,3]oxazin-6-yl)-2-(4-(4-(trifluoromethoxy)phenoxy)piperidin-1-yl)acetamide

Guidance literature:: Multi-step reaction with 2 steps

1: triphenylphosphine; di-isopropyl azodicarboxylate / tetrahydrofuran / 20 °C / Cooling with ice

2: potassium carbonate / N,N-dimethyl-formamide / 50 °C / Inert atmosphere

With di-isopropyl azodicarboxylate; potassium carbonate; triphenylphosphine; In tetrahydrofuran; N,N-dimethyl-formamide;