(E)-N-(4-methyl-2-(4-(3-methyl-2-oxoimidazolidin-1-yl)piperidin-1-yl) quinazolin-6-yl)-3-(4-(trifluoromethoxy)phenyl)acrylamide

Base Information

Chemical Name:(E)-N-(4-methyl-2-(4-(3-methyl-2-oxoimidazolidin-1-yl)piperidin-1-yl) quinazolin-6-yl)-3-(4-(trifluoromethoxy)phenyl)acrylamide
CAS No.:1374856-19-5
Molecular Formula:C₂₈H₂₉F₃N₆O₃
Molecular Weight:554.572
Hs Code.:

Synonyms:(E)-N-(4-methyl-2-(4-(3-methyl-2-oxoimidazolidin-1-yl)piperidin-1-yl) quinazolin-6-yl)-3-(4-(trifluoromethoxy)phenyl)acrylamide

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Chemical Property of (E)-N-(4-methyl-2-(4-(3-methyl-2-oxoimidazolidin-1-yl)piperidin-1-yl) quinazolin-6-yl)-3-(4-(trifluoromethoxy)phenyl)acrylamide

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Technology Process of (E)-N-(4-methyl-2-(4-(3-methyl-2-oxoimidazolidin-1-yl)piperidin-1-yl) quinazolin-6-yl)-3-(4-(trifluoromethoxy)phenyl)acrylamide

There total 9 articles about (E)-N-(4-methyl-2-(4-(3-methyl-2-oxoimidazolidin-1-yl)piperidin-1-yl) quinazolin-6-yl)-3-(4-(trifluoromethoxy)phenyl)acrylamide 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:

: 1374856-77-5
1-(1-(6-amino-4-methylquinazolin-2-yl)piperidin-4-yl)-3-methyl imidazolidin-2-one

: 199679-35-1
3-(4-trifluoromethoxyphenyl)acrylic acid

: 1374856-19-5
(E)-N-(4-methyl-2-(4-(3-methyl-2-oxoimidazolidin-1-yl)piperidin-1-yl) quinazolin-6-yl)-3-(4-(trifluoromethoxy)phenyl)acrylamide

Guidance literature:: With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; In dichloromethane; at 0 - 20 ℃; for 6h;
DOI:10.1016/j.bmcl.2012.03.049

Reference yield:

: 850172-43-9
4-methyl-6-nitroquinazolin-2-ol

: 1374856-19-5
(E)-N-(4-methyl-2-(4-(3-methyl-2-oxoimidazolidin-1-yl)piperidin-1-yl) quinazolin-6-yl)-3-(4-(trifluoromethoxy)phenyl)acrylamide

Guidance literature:: Multi-step reaction with 4 steps

1: trichlorophosphate / 2 h / 0 °C / Reflux

2: triethylamine / methanol / 2 h / Reflux

3: palladium 10% on activated carbon; hydrogen / ethanol / 2 h

4: benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine / dichloromethane / 6 h / 0 - 20 °C

With palladium 10% on activated carbon; hydrogen; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; trichlorophosphate; In methanol; ethanol; dichloromethane;
DOI:10.1016/j.bmcl.2012.03.049

Reference yield:

: 850172-44-0
2-chloro-4-methyl-6-nitroquinazoline

: 1374856-19-5
(E)-N-(4-methyl-2-(4-(3-methyl-2-oxoimidazolidin-1-yl)piperidin-1-yl) quinazolin-6-yl)-3-(4-(trifluoromethoxy)phenyl)acrylamide

Guidance literature:: Multi-step reaction with 3 steps

1: triethylamine / methanol / 2 h / Reflux

2: palladium 10% on activated carbon; hydrogen / ethanol / 2 h

3: benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine / dichloromethane / 6 h / 0 - 20 °C

With palladium 10% on activated carbon; hydrogen; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; In methanol; ethanol; dichloromethane;
DOI:10.1016/j.bmcl.2012.03.049