N-((3-cyanopyrazin-2-yl)(4-methoxy-3,5-dimethylphenyl)methylene)-2-methylpropane-2-sulfinamide

Base Information

Chemical Name:N-((3-cyanopyrazin-2-yl)(4-methoxy-3,5-dimethylphenyl)methylene)-2-methylpropane-2-sulfinamide
CAS No.:1260248-26-7
Molecular Formula:C₁₉H₂₂N₄O₂S
Molecular Weight:370.475
Hs Code.:

Synonyms:N-((3-cyanopyrazin-2-yl)(4-methoxy-3,5-dimethylphenyl)methylene)-2-methylpropane-2-sulfinamide

Suppliers and Price of N-((3-cyanopyrazin-2-yl)(4-methoxy-3,5-dimethylphenyl)methylene)-2-methylpropane-2-sulfinamide

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of N-((3-cyanopyrazin-2-yl)(4-methoxy-3,5-dimethylphenyl)methylene)-2-methylpropane-2-sulfinamide

Chemical Property:

Purity/Quality:: 98% ^*data from raw suppliers

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Technology Process of N-((3-cyanopyrazin-2-yl)(4-methoxy-3,5-dimethylphenyl)methylene)-2-methylpropane-2-sulfinamide

There total 2 articles about N-((3-cyanopyrazin-2-yl)(4-methoxy-3,5-dimethylphenyl)methylene)-2-methylpropane-2-sulfinamide 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:

: 67367-37-7
3-amidecarbonylpyrazine-2-carboxylic acid

: 1260248-26-7
N-((3-cyanopyrazin-2-yl)(4-methoxy-3,5-dimethylphenyl)methylene)-2-methylpropane-2-sulfinamide

Guidance literature:: Multi-step reaction with 3 steps

1.1: triethylamine / dichloromethane / 0 - 20 °C

2.1: magnesium; lithium chloride / diisobutylaluminium hydride / tetrahydrofuran / 3 h / Inert atmosphere

2.2: 1.33 h / -78 °C

3.1: titanium(IV) tetraethanolate / tetrahydrofuran / 72 h / 60 °C

3.2: 0.17 h / 20 °C

With magnesium; triethylamine; lithium chloride; titanium(IV) tetraethanolate; diisobutylaluminium hydride; In tetrahydrofuran; dichloromethane;

Reference yield:

: 74402-57-6
methyl 3-cyanopyrazine-2-carboxylate

: 1260248-26-7
N-((3-cyanopyrazin-2-yl)(4-methoxy-3,5-dimethylphenyl)methylene)-2-methylpropane-2-sulfinamide

Guidance literature:: Multi-step reaction with 2 steps

1.1: magnesium; lithium chloride / diisobutylaluminium hydride / tetrahydrofuran / 3 h / Inert atmosphere

1.2: 1.33 h / -78 °C

2.1: titanium(IV) tetraethanolate / tetrahydrofuran / 72 h / 60 °C

2.2: 0.17 h / 20 °C

With magnesium; lithium chloride; titanium(IV) tetraethanolate; diisobutylaluminium hydride; In tetrahydrofuran;

Reference yield: 79.0%

: 591-18-4
1-Bromo-3-iodobenzene

: 1260248-26-7
N-((3-cyanopyrazin-2-yl)(4-methoxy-3,5-dimethylphenyl)methylene)-2-methylpropane-2-sulfinamide

: 1260248-27-8
5-(3-bromophenyl)-5-(4-methoxy-3,5-dimethylphenyl)-5H-pyrrolo[3,4-b]pyrazin-7-amine

Guidance literature:: 1-Bromo-3-iodobenzene; With magnesium; lithium chloride; diisobutylaluminium hydride; In tetrahydrofuran; for 1.5h; Inert atmosphere;

N-((3-cyanopyrazin-2-yl)(4-methoxy-3,5-dimethylphenyl)methylene)-2-methylpropane-2-sulfinamide; In tetrahydrofuran; at -20 - 20 ℃;

With hydrogenchloride; In tetrahydrofuran; methanol; for 1h;