8-(piperazin-1-yl)-1-(thiophen-2-yl)-5-(2,3,6-trifluorophenyl)indeno[1,2-d]pyrazolo[3,4-b]pyridin-6(3H)-one

Base Information

Chemical Name:8-(piperazin-1-yl)-1-(thiophen-2-yl)-5-(2,3,6-trifluorophenyl)indeno[1,2-d]pyrazolo[3,4-b]pyridin-6(3H)-one
CAS No.:1403500-26-4
Molecular Formula:C₂₇H₁₈F₃N₅OS
Molecular Weight:517.534
Hs Code.:

Synonyms:8-(piperazin-1-yl)-1-(thiophen-2-yl)-5-(2,3,6-trifluorophenyl)indeno[1,2-d]pyrazolo[3,4-b]pyridin-6(3H)-one

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Chemical Property of 8-(piperazin-1-yl)-1-(thiophen-2-yl)-5-(2,3,6-trifluorophenyl)indeno[1,2-d]pyrazolo[3,4-b]pyridin-6(3H)-one

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Technology Process of 8-(piperazin-1-yl)-1-(thiophen-2-yl)-5-(2,3,6-trifluorophenyl)indeno[1,2-d]pyrazolo[3,4-b]pyridin-6(3H)-one

There total 4 articles about 8-(piperazin-1-yl)-1-(thiophen-2-yl)-5-(2,3,6-trifluorophenyl)indeno[1,2-d]pyrazolo[3,4-b]pyridin-6(3H)-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: 3.0%

: 1403501-15-4
ethyl 4-(4-(4-(tert-butoxycarbonyl)piperazin-1-yl)phenyl)-3-(thiophen-2-yl)-6-(2,3,6-trifluorophenyl)-4,7-dihydro-1H-pyrazolo[3,4-b]pyridine-5-carboxylate

: 1403500-26-4
8-(piperazin-1-yl)-1-(thiophen-2-yl)-5-(2,3,6-trifluorophenyl)indeno[1,2-d]pyrazolo[3,4-b]pyridin-6(3H)-one

Guidance literature:: ethyl 4-(4-(4-(tert-butoxycarbonyl)piperazin-1-yl)phenyl)-3-(thiophen-2-yl)-6-(2,3,6-trifluorophenyl)-4,7-dihydro-1H-pyrazolo[3,4-b]pyridine-5-carboxylate; In xylene; at 160 ℃; for 36h;

With sodium hydrogencarbonate; In water; xylene;

Reference yield:

: 189807-20-3
2,3,6-trifluorobenzoyl chloride

: 1403500-26-4
8-(piperazin-1-yl)-1-(thiophen-2-yl)-5-(2,3,6-trifluorophenyl)indeno[1,2-d]pyrazolo[3,4-b]pyridin-6(3H)-one

Guidance literature:: Multi-step reaction with 3 steps

1.1: triethylamine; magnesium chloride / acetonitrile / 5 h / 0 - 20 °C / Inert atmosphere

1.2: 18 h / 0 - 20 °C

2.1: ammonium acetate / 1 h / 120 °C / Sealed tube

3.1: polyphosphoric acid / xylene / 36 h / 160 °C

With ammonium acetate; triethylamine; magnesium chloride; In acetonitrile; xylene;

Reference yield:

: 197638-83-8
4-(4-(1,1-dimethylethoxycarbonyl)piperazinyl)benzaldehyde

: 1403500-26-4
8-(piperazin-1-yl)-1-(thiophen-2-yl)-5-(2,3,6-trifluorophenyl)indeno[1,2-d]pyrazolo[3,4-b]pyridin-6(3H)-one

Guidance literature:: Multi-step reaction with 2 steps

1: ammonium acetate / 1 h / 120 °C / Sealed tube

2: polyphosphoric acid / xylene / 36 h / 160 °C

With ammonium acetate; In xylene;