1-(2-(p-trifluoromethylphenyl)-quinazolin-4-yl)-2-naphthyl(trifluoromethyl)sulfonate

Base Information

Chemical Name:1-(2-(p-trifluoromethylphenyl)-quinazolin-4-yl)-2-naphthyl(trifluoromethyl)sulfonate
CAS No.:1242459-67-1
Molecular Formula:C₂₆H₁₄F₆N₂O₃S
Molecular Weight:548.465
Hs Code.:

Synonyms:1-(2-(p-trifluoromethylphenyl)-quinazolin-4-yl)-2-naphthyl(trifluoromethyl)sulfonate

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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 1-(2-(p-trifluoromethylphenyl)-quinazolin-4-yl)-2-naphthyl(trifluoromethyl)sulfonate

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Technology Process of 1-(2-(p-trifluoromethylphenyl)-quinazolin-4-yl)-2-naphthyl(trifluoromethyl)sulfonate

There total 1 articles about 1-(2-(p-trifluoromethylphenyl)-quinazolin-4-yl)-2-naphthyl(trifluoromethyl)sulfonate 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: 92.0%

: 358-23-6
trifluoromethylsulfonic anhydride

: 1242459-63-7
1-(2-(p-trifluoromethylphenyl)-quinazolin-4-yl)-naphthalen-2-ol

: 1242459-67-1
1-(2-(p-trifluoromethylphenyl)-quinazolin-4-yl)-2-naphthyl(trifluoromethyl)sulfonate

Guidance literature:: With dmap; In dichloromethane; at 20 ℃; Inert atmosphere;
DOI:10.1016/j.tetasy.2010.06.012

Reference yield: 65.0%

: 1242459-67-1
1-(2-(p-trifluoromethylphenyl)-quinazolin-4-yl)-2-naphthyl(trifluoromethyl)sulfonate

: 829-85-6
diphenylphosphane

: 1242459-72-8,1243257-84-2
(R,S)-diphenyl(1-(2-(p-trifluoromethylphenyl)-quinazolin-4-yl)(2-naphthyl))phosphine

Guidance literature:: With 1,4-diaza-bicyclo[2.2.2]octane; 1,2-bis(diphenylphosphino)ethane nickel(II) chloride; In N,N-dimethyl-formamide; at 100 ℃; for 73h; Inert atmosphere;
DOI:10.1016/j.tetasy.2010.06.012