3-(1-methyl-1H-indol-3-yl)-4-(1H-pyrazolo[3,4-b]pyridin-3-yl)-1-phenyl-1H-pyrrole-2,5-dione

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Chemical Name:3-(1-methyl-1H-indol-3-yl)-4-(1H-pyrazolo[3,4-b]pyridin-3-yl)-1-phenyl-1H-pyrrole-2,5-dione
CAS No.:1178564-35-6
Molecular Formula:C₂₅H₁₇N₅O₂
Molecular Weight:419.442
Hs Code.:

Synonyms:3-(1-methyl-1H-indol-3-yl)-4-(1H-pyrazolo[3,4-b]pyridin-3-yl)-1-phenyl-1H-pyrrole-2,5-dione

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Chemical Property of 3-(1-methyl-1H-indol-3-yl)-4-(1H-pyrazolo[3,4-b]pyridin-3-yl)-1-phenyl-1H-pyrrole-2,5-dione

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Technology Process of 3-(1-methyl-1H-indol-3-yl)-4-(1H-pyrazolo[3,4-b]pyridin-3-yl)-1-phenyl-1H-pyrrole-2,5-dione

There total 6 articles about 3-(1-methyl-1H-indol-3-yl)-4-(1H-pyrazolo[3,4-b]pyridin-3-yl)-1-phenyl-1H-pyrrole-2,5-dione 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: 55.0%

: 1178564-34-5
3-chloro-4-(1-methyl-1H-indol-3-yl)-1-phenyl-1H-pyrrole-2,5-dione

: 1178564-33-4
3-(tributylstannanyl)-1H-pyrazolo[3,4-b]pyridine

: 1178564-35-6
3-(1-methyl-1H-indol-3-yl)-4-(1H-pyrazolo[3,4-b]pyridin-3-yl)-1-phenyl-1H-pyrrole-2,5-dione

Guidance literature:: With palladium-based catalyst; lithium chloride; In toluene; at 100 ℃; for 10h; Inert atmosphere;
DOI:10.1016/j.bmc.2009.04.043

Reference yield:

: 6602-54-6
2-chloro-3-pyridinecarbonitrile

: 1178564-35-6
3-(1-methyl-1H-indol-3-yl)-4-(1H-pyrazolo[3,4-b]pyridin-3-yl)-1-phenyl-1H-pyrrole-2,5-dione

Guidance literature:: Multi-step reaction with 6 steps

1: hydrazine / ethanol / Reflux

2: 1-nitroisobutane; tetrafluoroboric acid / methanol / 0 - 5 °C

3: phosphinic acid / water / 20 °C

4: iodine; potassium hydroxide / N,N-dimethyl-formamide / 20 °C

5: ethylmagnesium bromide / tetrahydrofuran / -5 - 0 °C

6: lithium chloride; bis(triphenylphosphine)palladium(II) chloride / toluene / 10 h / 100 °C

With tetrafluoroboric acid; phosphinic acid; bis(triphenylphosphine)palladium(II) chloride; 1-nitroisobutane; ethylmagnesium bromide; iodine; lithium chloride; potassium hydroxide; hydrazine; In tetrahydrofuran; methanol; ethanol; water; N,N-dimethyl-formamide; toluene;
DOI:10.1016/j.ejmech.2013.07.046

Reference yield:

: 6752-16-5
1H-pyrazolo[3,4-b]pyridin-3-amine

: 1178564-35-6
3-(1-methyl-1H-indol-3-yl)-4-(1H-pyrazolo[3,4-b]pyridin-3-yl)-1-phenyl-1H-pyrrole-2,5-dione

Guidance literature:: Multi-step reaction with 5 steps

1: 1-nitroisobutane; tetrafluoroboric acid / methanol / 0 - 5 °C

2: phosphinic acid / water / 20 °C

3: iodine; potassium hydroxide / N,N-dimethyl-formamide / 20 °C

4: ethylmagnesium bromide / tetrahydrofuran / -5 - 0 °C

5: lithium chloride; bis(triphenylphosphine)palladium(II) chloride / toluene / 10 h / 100 °C

With tetrafluoroboric acid; phosphinic acid; bis(triphenylphosphine)palladium(II) chloride; 1-nitroisobutane; ethylmagnesium bromide; iodine; lithium chloride; potassium hydroxide; In tetrahydrofuran; methanol; water; N,N-dimethyl-formamide; toluene;
DOI:10.1016/j.ejmech.2013.07.046