N-{4-[2-cyano-2-(4-fluoro-phenyl)-1-hydroxy-vinyl]-pyridin-2-yl}-acetamide

Base Information

Chemical Name:N-{4-[2-cyano-2-(4-fluoro-phenyl)-1-hydroxy-vinyl]-pyridin-2-yl}-acetamide
CAS No.:549505-57-9
Molecular Formula:C₁₆H₁₂FN₃O₂
Molecular Weight:297.289
Hs Code.:

<i>N</i>-{4-[2-cyano-2-(4-fluoro-phenyl)-1-hydroxy-vinyl]-pyridin-2-yl}-acetamide

Synonyms:N-{4-[2-cyano-2-(4-fluoro-phenyl)-1-hydroxy-vinyl]-pyridin-2-yl}-acetamide

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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-{4-[2-cyano-2-(4-fluoro-phenyl)-1-hydroxy-vinyl]-pyridin-2-yl}-acetamide

Chemical Property:

Purity/Quality:

Safty Information:

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Hazard Codes:

MSDS Files:: SDS file from LookChem

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Technology Process of N-{4-[2-cyano-2-(4-fluoro-phenyl)-1-hydroxy-vinyl]-pyridin-2-yl}-acetamide

There total 2 articles about N-{4-[2-cyano-2-(4-fluoro-phenyl)-1-hydroxy-vinyl]-pyridin-2-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: 65.0%

: 459-22-3
4-fluorophenylacetonitrile

: 54221-95-3
2-(acetylamino)isonicotinic acid

: 549505-57-9
N-{4-[2-cyano-2-(4-fluoro-phenyl)-1-hydroxy-vinyl]-pyridin-2-yl}-acetamide

Guidance literature:: 2-(acetylamino)isonicotinic acid; With 1,1'-carbonyldiimidazole; In N,N-dimethyl-formamide; at 20 ℃; for 0.75h;

4-fluorophenylacetonitrile; With potassium tert-butylate; In N,N-dimethyl-formamide; at 120 ℃; for 2h;
DOI:10.1021/jo026619w

Reference yield:

: 695-34-1
2-Amino-4-methylpyridine

: 549505-57-9
N-{4-[2-cyano-2-(4-fluoro-phenyl)-1-hydroxy-vinyl]-pyridin-2-yl}-acetamide

Guidance literature:: Multi-step reaction with 3 steps

1.1: 75 percent / 4-dimethylaminopyridine / 5 h / Heating

2.1: 42 percent / potassium permanganate / H₂O / 2.5 h / 50 - 90 °C

3.1: carbonyldiimidazole / dimethylformamide / 0.75 h / 20 °C

3.2: 65 percent / potassium tert-butoxide / dimethylformamide / 2 h / 120 °C

With dmap; potassium permanganate; 1,1'-carbonyldiimidazole; In water; N,N-dimethyl-formamide;
DOI:10.1021/jo026619w