[7-(1H-imidazol-1-yl)-5-(4-methoxyphenyl)pyrazolo[1,5-a]pyrimidin-3-yl][4-[(2,3,5-trifluorophenyl)methyl]-1-piperazinyl]methanone

Base Information

Chemical Name:[7-(1H-imidazol-1-yl)-5-(4-methoxyphenyl)pyrazolo[1,5-a]pyrimidin-3-yl][4-[(2,3,5-trifluorophenyl)methyl]-1-piperazinyl]methanone
CAS No.:1076205-13-4
Molecular Formula:C₂₈H₂₄F₃N₇O₂
Molecular Weight:547.539
Hs Code.:

Synonyms:[7-(1H-imidazol-1-yl)-5-(4-methoxyphenyl)pyrazolo[1,5-a]pyrimidin-3-yl][4-[(2,3,5-trifluorophenyl)methyl]-1-piperazinyl]methanone

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Chemical Property of [7-(1H-imidazol-1-yl)-5-(4-methoxyphenyl)pyrazolo[1,5-a]pyrimidin-3-yl][4-[(2,3,5-trifluorophenyl)methyl]-1-piperazinyl]methanone

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Technology Process of [7-(1H-imidazol-1-yl)-5-(4-methoxyphenyl)pyrazolo[1,5-a]pyrimidin-3-yl][4-[(2,3,5-trifluorophenyl)methyl]-1-piperazinyl]methanone

There total 8 articles about [7-(1H-imidazol-1-yl)-5-(4-methoxyphenyl)pyrazolo[1,5-a]pyrimidin-3-yl][4-[(2,3,5-trifluorophenyl)methyl]-1-piperazinyl]methanone 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:

: 288-32-4
1H-imidazole

: [7-chloro-5-(4-methoxyphenyl)pyrazolo[1,5-a]pyrimidin-3-yl][4-[(2,3,5-trifluorophenyl)methyl]-1-piperazinyl]methanone hydrochloride

: 1076205-13-4
[7-(1H-imidazol-1-yl)-5-(4-methoxyphenyl)pyrazolo[1,5-a]pyrimidin-3-yl][4-[(2,3,5-trifluorophenyl)methyl]-1-piperazinyl]methanone

Guidance literature:: In N,N-dimethyl-formamide; at 20 - 80 ℃; for 2h;

Reference yield:

: 1076206-26-2
7-chloro-5-(4-methoxyphenyl)pyrazolo[1,5-a]pyrimidine-3-carbonyl chloride

: 1076205-13-4
[7-(1H-imidazol-1-yl)-5-(4-methoxyphenyl)pyrazolo[1,5-a]pyrimidin-3-yl][4-[(2,3,5-trifluorophenyl)methyl]-1-piperazinyl]methanone

Guidance literature:: Multi-step reaction with 2 steps

1: triethylamine / dichloromethane / 2 - 4 h / 0 - 20 °C

2: N,N-dimethyl-formamide / 2 h / 20 - 80 °C

With triethylamine; In dichloromethane; N,N-dimethyl-formamide;

Reference yield:

: 1076206-24-0
4,7-dihydro-5-(4-methoxyphenyl)-7-oxopyrazolo[1,5-a]pyrimidine-3-carboxylic acid ethyl ester

: 1076205-13-4
[7-(1H-imidazol-1-yl)-5-(4-methoxyphenyl)pyrazolo[1,5-a]pyrimidin-3-yl][4-[(2,3,5-trifluorophenyl)methyl]-1-piperazinyl]methanone

Guidance literature:: Multi-step reaction with 4 steps

1: ethanol; water / 4 - 16 h / 70 °C

2: trichlorophosphate / 16 - 24 h / 70 °C

3: triethylamine / dichloromethane / 2 - 4 h / 0 - 20 °C

4: N,N-dimethyl-formamide / 2 h / 20 - 80 °C

With ethanol; water; triethylamine; trichlorophosphate; In dichloromethane; N,N-dimethyl-formamide;