2-(4-(4-(4-(trifluoromethyl)phenylsulfonyl)piperazine-1-carbonyl)phenyl)quinazolin-4(3H)-one

Base Information

Chemical Name:2-(4-(4-(4-(trifluoromethyl)phenylsulfonyl)piperazine-1-carbonyl)phenyl)quinazolin-4(3H)-one
CAS No.:1335015-75-2
Molecular Formula:C₂₆H₂₁F₃N₄O₄S
Molecular Weight:542.538
Hs Code.:

Synonyms:2-(4-(4-(4-(trifluoromethyl)phenylsulfonyl)piperazine-1-carbonyl)phenyl)quinazolin-4(3H)-one

Suppliers and Price of 2-(4-(4-(4-(trifluoromethyl)phenylsulfonyl)piperazine-1-carbonyl)phenyl)quinazolin-4(3H)-one

Supply Marketing:

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

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 0 raw suppliers

Chemical Property of 2-(4-(4-(4-(trifluoromethyl)phenylsulfonyl)piperazine-1-carbonyl)phenyl)quinazolin-4(3H)-one

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of 2-(4-(4-(4-(trifluoromethyl)phenylsulfonyl)piperazine-1-carbonyl)phenyl)quinazolin-4(3H)-one

There total 6 articles about 2-(4-(4-(4-(trifluoromethyl)phenylsulfonyl)piperazine-1-carbonyl)phenyl)quinazolin-4(3H)-one 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: 33.0%

: 2991-42-6
4-trifluorophenylsulfonyl chloride

: 1335014-09-9
2-(4-(piperazine-1-carbonyl)phenyl) quinazolin-4(3H)-one

: 1335015-75-2
2-(4-(4-(4-(trifluoromethyl)phenylsulfonyl)piperazine-1-carbonyl)phenyl)quinazolin-4(3H)-one

Guidance literature:: 2-(4-(piperazine-1-carbonyl)phenyl) quinazolin-4(3H)-one; With sodium hydride; In N,N-dimethyl-formamide; mineral oil; at 100 ℃;

4-trifluorophenylsulfonyl chloride; In N,N-dimethyl-formamide; mineral oil; at 100 ℃; for 16h;
DOI:10.1016/j.ejmech.2011.05.061

Reference yield:

: 374711-37-2
4-(4-oxo-3,4-dihydroquinazolin-2-yl)benzoic acid

: 1335015-75-2
2-(4-(4-(4-(trifluoromethyl)phenylsulfonyl)piperazine-1-carbonyl)phenyl)quinazolin-4(3H)-one

Guidance literature:: Multi-step reaction with 3 steps

1.1: benzotriazol-1-yloxyl-tris-(pyrrolidino)-phosphonium hexafluorophosphate; N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide / 20 h / 20 °C

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

3.1: sodium hydride / N,N-dimethyl-formamide; mineral oil / 100 °C

3.2: 16 h / 100 °C

With hydrogenchloride; benzotriazol-1-yloxyl-tris-(pyrrolidino)-phosphonium hexafluorophosphate; sodium hydride; N-ethyl-N,N-diisopropylamine; In 1,4-dioxane; chloroform; N,N-dimethyl-formamide; mineral oil;
DOI:10.1016/j.ejmech.2011.05.061

Reference yield:

: 1335014-00-0
tert-butyl 4-(4-(4-oxo-3,4-dihydroquinazolin-2-yl)benzoyl)piperazine-1-carboxylate

: 1335015-75-2
2-(4-(4-(4-(trifluoromethyl)phenylsulfonyl)piperazine-1-carbonyl)phenyl)quinazolin-4(3H)-one

Guidance literature:: Multi-step reaction with 2 steps

1.1: hydrogenchloride / 1,4-dioxane; chloroform / 3 h / 20 °C

2.1: sodium hydride / N,N-dimethyl-formamide; mineral oil / 100 °C

2.2: 16 h / 100 °C

With hydrogenchloride; sodium hydride; In 1,4-dioxane; chloroform; N,N-dimethyl-formamide; mineral oil;
DOI:10.1016/j.ejmech.2011.05.061