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

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Chemical Name:ethyl 4-(4-(4-(tert-butoxycarbonyl)piperazin-1-yl)phenyl)-3-(thiophen-2-yl)-6-(2,3,6-trifluorophenyl)-1H-pyrazolo[3,4-b]pyridine-5-carboxylate
CAS No.:1403501-16-5
Molecular Formula:C₃₄H₃₂F₃N₅O₄S
Molecular Weight:663.72
Hs Code.:

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

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Chemical Property of ethyl 4-(4-(4-(tert-butoxycarbonyl)piperazin-1-yl)phenyl)-3-(thiophen-2-yl)-6-(2,3,6-trifluorophenyl)-1H-pyrazolo[3,4-b]pyridine-5-carboxylate

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Technology Process of ethyl 4-(4-(4-(tert-butoxycarbonyl)piperazin-1-yl)phenyl)-3-(thiophen-2-yl)-6-(2,3,6-trifluorophenyl)-1H-pyrazolo[3,4-b]pyridine-5-carboxylate

There total 5 articles about ethyl 4-(4-(4-(tert-butoxycarbonyl)piperazin-1-yl)phenyl)-3-(thiophen-2-yl)-6-(2,3,6-trifluorophenyl)-1H-pyrazolo[3,4-b]pyridine-5-carboxylate 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: 85.0%

: 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

: 1403501-16-5
ethyl 4-(4-(4-(tert-butoxycarbonyl)piperazin-1-yl)phenyl)-3-(thiophen-2-yl)-6-(2,3,6-trifluorophenyl)-1H-pyrazolo[3,4-b]pyridine-5-carboxylate

Guidance literature:: With manganese(II) oxide; In dichloromethane; at 20 ℃; for 20h;

Reference yield:

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

: 1403501-16-5
ethyl 4-(4-(4-(tert-butoxycarbonyl)piperazin-1-yl)phenyl)-3-(thiophen-2-yl)-6-(2,3,6-trifluorophenyl)-1H-pyrazolo[3,4-b]pyridine-5-carboxylate

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: manganese(II) oxide / dichloromethane / 20 h / 20 °C

With ammonium acetate; manganese(II) oxide; triethylamine; magnesium chloride; In dichloromethane; acetonitrile;

Reference yield:

: ethyl 3-(2,3,6-trifluorophenyl)-3-oxopropanoate

: 1403501-16-5
ethyl 4-(4-(4-(tert-butoxycarbonyl)piperazin-1-yl)phenyl)-3-(thiophen-2-yl)-6-(2,3,6-trifluorophenyl)-1H-pyrazolo[3,4-b]pyridine-5-carboxylate

Guidance literature:: Multi-step reaction with 2 steps

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

2: manganese(II) oxide / dichloromethane / 20 h / 20 °C

With ammonium acetate; manganese(II) oxide; In dichloromethane;