2-fluoro-N-(6-(3-(4-fluorophenyl)-1-methyl-5-(4-(3,3,3-trifluoropropyl)piperazin-1-yl)-1H-pyrazol-4-yl)imidazo[1,2-b]pyridazin-2-yl)isonicotinamide

Base Information

Chemical Name:2-fluoro-N-(6-(3-(4-fluorophenyl)-1-methyl-5-(4-(3,3,3-trifluoropropyl)piperazin-1-yl)-1H-pyrazol-4-yl)imidazo[1,2-b]pyridazin-2-yl)isonicotinamide
CAS No.:1616234-40-2
Molecular Formula:C₂₉H₂₆F₅N₉O
Molecular Weight:611.577
Hs Code.:

Synonyms:2-fluoro-N-(6-(3-(4-fluorophenyl)-1-methyl-5-(4-(3,3,3-trifluoropropyl)piperazin-1-yl)-1H-pyrazol-4-yl)imidazo[1,2-b]pyridazin-2-yl)isonicotinamide

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Chemical Property of 2-fluoro-N-(6-(3-(4-fluorophenyl)-1-methyl-5-(4-(3,3,3-trifluoropropyl)piperazin-1-yl)-1H-pyrazol-4-yl)imidazo[1,2-b]pyridazin-2-yl)isonicotinamide

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Technology Process of 2-fluoro-N-(6-(3-(4-fluorophenyl)-1-methyl-5-(4-(3,3,3-trifluoropropyl)piperazin-1-yl)-1H-pyrazol-4-yl)imidazo[1,2-b]pyridazin-2-yl)isonicotinamide

There total 13 articles about 2-fluoro-N-(6-(3-(4-fluorophenyl)-1-methyl-5-(4-(3,3,3-trifluoropropyl)piperazin-1-yl)-1H-pyrazol-4-yl)imidazo[1,2-b]pyridazin-2-yl)isonicotinamide 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: 24.0%

: 460-40-2
3,3,3-trifluoropropanal

: 1616245-46-5
2-fluoro-N-(6-(3-(4-fluorophenyl)-1-methyl-5-(piperazin-1-yl)-1H-pyrazol-4-yl)imidazo[1,2-b]pyridazin-2-yl)isonicotinamide

: 1616234-40-2
2-fluoro-N-(6-(3-(4-fluorophenyl)-1-methyl-5-(4-(3,3,3-trifluoropropyl)piperazin-1-yl)-1H-pyrazol-4-yl)imidazo[1,2-b]pyridazin-2-yl)isonicotinamide

Guidance literature:: With sodium cyanoborohydride; In tetrahydrofuran; methanol; at 20 ℃;

Reference yield:

: 1616234-39-9
tert-butyl 4-(4-(2-(2-fluoroisonicotinamido)imidazo[1,2-b]pyridazin-6-yl)-3-(4-fluorophenyl)-1-methyl-1H-pyrazol-5-yl)piperazine-1-carboxylate

: 1616234-40-2
2-fluoro-N-(6-(3-(4-fluorophenyl)-1-methyl-5-(4-(3,3,3-trifluoropropyl)piperazin-1-yl)-1H-pyrazol-4-yl)imidazo[1,2-b]pyridazin-2-yl)isonicotinamide

Guidance literature:: Multi-step reaction with 2 steps

1: trifluoroacetic acid / dichloromethane / 20 °C

2: sodium cyanoborohydride / tetrahydrofuran; methanol / 20 °C

With sodium cyanoborohydride; trifluoroacetic acid; In tetrahydrofuran; methanol; dichloromethane;

Reference yield:

: 1616235-36-9
tert-butyl 4-(1-methylhydrazinecarbonothioyl)piperazine-1-carboxylate

: 1616234-40-2
2-fluoro-N-(6-(3-(4-fluorophenyl)-1-methyl-5-(4-(3,3,3-trifluoropropyl)piperazin-1-yl)-1H-pyrazol-4-yl)imidazo[1,2-b]pyridazin-2-yl)isonicotinamide

Guidance literature:: Multi-step reaction with 9 steps

1.1: ethanol / 0 - 20 °C

1.2: 80 °C

2.1: dmap / dichloromethane / 0.5 h / 20 °C

3.1: N-Bromosuccinimide / dichloromethane / 1 h / 20 °C

4.1: potassium phosphate; dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH₂Cl₂ / 1,4-dioxane; water / 100 °C / Inert atmosphere

5.1: hydrogenchloride; methanol / 20 °C

6.1: N-ethyl-N,N-diisopropylamine / dichloromethane / 4 h / 20 °C

7.1: N-ethyl-N,N-diisopropylamine; HATU / N,N-dimethyl-formamide / 20 °C

8.1: trifluoroacetic acid / dichloromethane / 20 °C

9.1: sodium cyanoborohydride / tetrahydrofuran; methanol / 20 °C

With hydrogenchloride; methanol; dmap; potassium phosphate; N-Bromosuccinimide; dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH₂Cl₂; sodium cyanoborohydride; N-ethyl-N,N-diisopropylamine; HATU; trifluoroacetic acid; In tetrahydrofuran; 1,4-dioxane; methanol; ethanol; dichloromethane; water; N,N-dimethyl-formamide;