N-(4-(1-benzyl-7-oxo-1,6,7,8-tetrahydropyrazolo[4,3-b][1,4]diazepin-5-yl)phenyl)-3-(4-methyl-1H-imidazol-1-yl)-5-(trifluoromethyl)benzamide

Base Information

Chemical Name:N-(4-(1-benzyl-7-oxo-1,6,7,8-tetrahydropyrazolo[4,3-b][1,4]diazepin-5-yl)phenyl)-3-(4-methyl-1H-imidazol-1-yl)-5-(trifluoromethyl)benzamide
CAS No.:1346441-05-1
Molecular Formula:C₃₁H₂₄F₃N₇O₂
Molecular Weight:583.572
Hs Code.:

Synonyms:N-(4-(1-benzyl-7-oxo-1,6,7,8-tetrahydropyrazolo[4,3-b][1,4]diazepin-5-yl)phenyl)-3-(4-methyl-1H-imidazol-1-yl)-5-(trifluoromethyl)benzamide

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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-(1-benzyl-7-oxo-1,6,7,8-tetrahydropyrazolo[4,3-b][1,4]diazepin-5-yl)phenyl)-3-(4-methyl-1H-imidazol-1-yl)-5-(trifluoromethyl)benzamide

Chemical Property:

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

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Technology Process of N-(4-(1-benzyl-7-oxo-1,6,7,8-tetrahydropyrazolo[4,3-b][1,4]diazepin-5-yl)phenyl)-3-(4-methyl-1H-imidazol-1-yl)-5-(trifluoromethyl)benzamide

There total 5 articles about N-(4-(1-benzyl-7-oxo-1,6,7,8-tetrahydropyrazolo[4,3-b][1,4]diazepin-5-yl)phenyl)-3-(4-methyl-1H-imidazol-1-yl)-5-(trifluoromethyl)benzamide 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:

: 641571-13-3
3-(4-methyl-imidazol-1-yl)-5-trifluoromethylbenzoic acid

: 1346441-48-2
C₁₉H₁₇N₅O

: 1346441-05-1
N-(4-(1-benzyl-7-oxo-1,6,7,8-tetrahydropyrazolo[4,3-b][1,4]diazepin-5-yl)phenyl)-3-(4-methyl-1H-imidazol-1-yl)-5-(trifluoromethyl)benzamide

Guidance literature:: With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; In N,N-dimethyl-formamide; at 20 ℃;
DOI:10.1016/j.bmc.2011.09.042

Reference yield:

: 838-57-3
ethyl 4-nitrobenzoylacetate

: 1346441-05-1
N-(4-(1-benzyl-7-oxo-1,6,7,8-tetrahydropyrazolo[4,3-b][1,4]diazepin-5-yl)phenyl)-3-(4-methyl-1H-imidazol-1-yl)-5-(trifluoromethyl)benzamide

Guidance literature:: Multi-step reaction with 3 steps

1: acetic acid / dichloromethane / 0.5 h / 20 °C

2: iron; ammonium chloride / tetrahydrofuran; water / 3 h / 60 °C

3: benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine / N,N-dimethyl-formamide / 20 °C

With iron; ammonium chloride; benzotriazol-1-ol; acetic acid; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; In tetrahydrofuran; dichloromethane; water; N,N-dimethyl-formamide;
DOI:10.1016/j.bmc.2011.09.042

Reference yield:

: C₁₉H₁₅N₅O₃

: 1346441-05-1
N-(4-(1-benzyl-7-oxo-1,6,7,8-tetrahydropyrazolo[4,3-b][1,4]diazepin-5-yl)phenyl)-3-(4-methyl-1H-imidazol-1-yl)-5-(trifluoromethyl)benzamide

Guidance literature:: Multi-step reaction with 2 steps

1: iron; ammonium chloride / tetrahydrofuran; water / 3 h / 60 °C

2: benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine / N,N-dimethyl-formamide / 20 °C

With iron; ammonium chloride; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; In tetrahydrofuran; water; N,N-dimethyl-formamide;
DOI:10.1016/j.bmc.2011.09.042