N-cyclopropyl-4-{8-[S-methyl-N-(trifluoroacetyl)sulfonimidoyl]-6-phenylimidazo[1,2-a]pyrazin-3-yl}benzamide

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Chemical Name:N-cyclopropyl-4-{8-[S-methyl-N-(trifluoroacetyl)sulfonimidoyl]-6-phenylimidazo[1,2-a]pyrazin-3-yl}benzamide
CAS No.:1334423-42-5
Molecular Formula:C₂₅H₂₀F₃N₅O₃S
Molecular Weight:527.527
Hs Code.:

Synonyms:N-cyclopropyl-4-{8-[S-methyl-N-(trifluoroacetyl)sulfonimidoyl]-6-phenylimidazo[1,2-a]pyrazin-3-yl}benzamide

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Chemical Property of N-cyclopropyl-4-{8-[S-methyl-N-(trifluoroacetyl)sulfonimidoyl]-6-phenylimidazo[1,2-a]pyrazin-3-yl}benzamide

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Technology Process of N-cyclopropyl-4-{8-[S-methyl-N-(trifluoroacetyl)sulfonimidoyl]-6-phenylimidazo[1,2-a]pyrazin-3-yl}benzamide

There total 6 articles about N-cyclopropyl-4-{8-[S-methyl-N-(trifluoroacetyl)sulfonimidoyl]-6-phenylimidazo[1,2-a]pyrazin-3-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: 16.0%

: 354-38-1
2,2,2-trifluoroacetamide

: 1334423-25-4
N-cyclopropyl-4-[8-(methylsulfinyl)-6-phenylimidazo[1,2-a]pyrazin-3-yl]benzamide

: 1334423-42-5
N-cyclopropyl-4-{8-[S-methyl-N-(trifluoroacetyl)sulfonimidoyl]-6-phenylimidazo[1,2-a]pyrazin-3-yl}benzamide

Guidance literature:: With [bis(acetoxy)iodo]benzene; magnesium oxide; dirhodium tetraacetate; In dichloromethane; at 23 ℃; for 39h; Inert atmosphere;

Reference yield:

: 887475-71-0
6-bromo-8-methylsulfanyl-imidazo[1,2-a]pyrazine

: 1334423-42-5
N-cyclopropyl-4-{8-[S-methyl-N-(trifluoroacetyl)sulfonimidoyl]-6-phenylimidazo[1,2-a]pyrazin-3-yl}benzamide

Guidance literature:: Multi-step reaction with 5 steps

1: N-iodo-succinimide / N,N-dimethyl-formamide / 6.5 h / 60 °C / Inert atmosphere

2: potassium phosphate / dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH₂Cl₂ / water; tetrahydrofuran / 16 h / 40 °C / Inert atmosphere

3: potassium carbonate; triphenylphosphine / 1-methyl-pyrrolidin-2-one; propan-1-ol / 2 h / 120 °C / Inert atmosphere

4: 3-chloro-benzenecarboperoxoic acid / dichloromethane / 1 h / 23 °C / Inert atmosphere

5: magnesium oxide; [bis(acetoxy)iodo]benzene / dirhodium tetraacetate / dichloromethane / 39 h / 23 °C / Inert atmosphere

With potassium phosphate; N-iodo-succinimide; [bis(acetoxy)iodo]benzene; magnesium oxide; potassium carbonate; 3-chloro-benzenecarboperoxoic acid; triphenylphosphine; dirhodium tetraacetate; dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH₂Cl₂; In tetrahydrofuran; 1-methyl-pyrrolidin-2-one; propan-1-ol; dichloromethane; water; N,N-dimethyl-formamide;

Reference yield:

: 1263425-46-2
4-(6-bromo-8-methylsulfanyl-imidazo[1,2-a]pyrazin-3-yl)-N-cyclopropyl-benzamide

: 1334423-42-5
N-cyclopropyl-4-{8-[S-methyl-N-(trifluoroacetyl)sulfonimidoyl]-6-phenylimidazo[1,2-a]pyrazin-3-yl}benzamide

Guidance literature:: Multi-step reaction with 3 steps

1: potassium carbonate; triphenylphosphine / 1-methyl-pyrrolidin-2-one; propan-1-ol / 2 h / 120 °C / Inert atmosphere

2: 3-chloro-benzenecarboperoxoic acid / dichloromethane / 1 h / 23 °C / Inert atmosphere

3: magnesium oxide; [bis(acetoxy)iodo]benzene / dirhodium tetraacetate / dichloromethane / 39 h / 23 °C / Inert atmosphere

With [bis(acetoxy)iodo]benzene; magnesium oxide; potassium carbonate; 3-chloro-benzenecarboperoxoic acid; triphenylphosphine; dirhodium tetraacetate; In 1-methyl-pyrrolidin-2-one; propan-1-ol; dichloromethane;