5-(3-(1H-imidazol-1-yl)propyl)-4-(4-bromophenyl)-3-phenyl-1-(2-((tetrahydro-2H-pyran-2-yl)oxy)ethyl)-4,5-dihydropyrrolo[3,4-c]pyrazol-6(1H)-one

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Chemical Name:5-(3-(1H-imidazol-1-yl)propyl)-4-(4-bromophenyl)-3-phenyl-1-(2-((tetrahydro-2H-pyran-2-yl)oxy)ethyl)-4,5-dihydropyrrolo[3,4-c]pyrazol-6(1H)-one
CAS No.:1542066-77-2
Molecular Formula:C₃₀H₃₂BrN₅O₃
Molecular Weight:590.52
Hs Code.:

5-(3-(1H-imidazol-1-yl)propyl)-4-(4-bromophenyl)-3-phenyl-1-(2-((tetrahydro-2H-pyran-2-yl)oxy)ethyl)-4,5-dihydropyrrolo[3,4-c]pyrazol-6(1H)-one

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Chemical Property of 5-(3-(1H-imidazol-1-yl)propyl)-4-(4-bromophenyl)-3-phenyl-1-(2-((tetrahydro-2H-pyran-2-yl)oxy)ethyl)-4,5-dihydropyrrolo[3,4-c]pyrazol-6(1H)-one

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Technology Process of 5-(3-(1H-imidazol-1-yl)propyl)-4-(4-bromophenyl)-3-phenyl-1-(2-((tetrahydro-2H-pyran-2-yl)oxy)ethyl)-4,5-dihydropyrrolo[3,4-c]pyrazol-6(1H)-one

There total 5 articles about 5-(3-(1H-imidazol-1-yl)propyl)-4-(4-bromophenyl)-3-phenyl-1-(2-((tetrahydro-2H-pyran-2-yl)oxy)ethyl)-4,5-dihydropyrrolo[3,4-c]pyrazol-6(1H)-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: 31.4%

: 1051871-37-4
5-(3-(1H-imidazol-1-yl)propyl)-4-(4-bromophenyl)-3-phenyl-4,5-dihydropyrrolo[3,4-c]pyrazol-6(1H)-one

: 1542066-77-2
5-(3-(1H-imidazol-1-yl)propyl)-4-(4-bromophenyl)-3-phenyl-1-(2-((tetrahydro-2H-pyran-2-yl)oxy)ethyl)-4,5-dihydropyrrolo[3,4-c]pyrazol-6(1H)-one

Guidance literature:: With potassium carbonate; In ethanol; for 8h; Reflux;
DOI:10.1021/jm401800k

Reference yield:

: 98-86-2
acetophenone

: 1542066-77-2
5-(3-(1H-imidazol-1-yl)propyl)-4-(4-bromophenyl)-3-phenyl-1-(2-((tetrahydro-2H-pyran-2-yl)oxy)ethyl)-4,5-dihydropyrrolo[3,4-c]pyrazol-6(1H)-one

Guidance literature:: Multi-step reaction with 4 steps

1.1: sodium methylate / methanol / 3 h / Reflux

2.1: 1,4-dioxane / 0.25 h

2.2: 12 h / 20 °C

3.1: hydrazine hydrate; acetic acid / 6.25 h / 0 °C / Reflux

4.1: potassium carbonate / ethanol / 8 h / Reflux

With sodium methylate; potassium carbonate; hydrazine hydrate; acetic acid; In 1,4-dioxane; methanol; ethanol;
DOI:10.1021/jm401800k

Reference yield:

: 41167-58-2
2-hydroxy-4-oxo-4-phenyl-but-2-enoic acid methyl ester

: 1542066-77-2
5-(3-(1H-imidazol-1-yl)propyl)-4-(4-bromophenyl)-3-phenyl-1-(2-((tetrahydro-2H-pyran-2-yl)oxy)ethyl)-4,5-dihydropyrrolo[3,4-c]pyrazol-6(1H)-one

Guidance literature:: Multi-step reaction with 3 steps

1.1: 1,4-dioxane / 0.25 h

1.2: 12 h / 20 °C

2.1: hydrazine hydrate; acetic acid / 6.25 h / 0 °C / Reflux

3.1: potassium carbonate / ethanol / 8 h / Reflux

With potassium carbonate; hydrazine hydrate; acetic acid; In 1,4-dioxane; ethanol;
DOI:10.1021/jm401800k