1-(6-(6-(2-(2,5-difluorophenyl)pyrrolidin-1-yl)imidazo[1,2-b]pyridazin-3-yl)pyridin-2-yl)piperidin-4-ol

Base Information

Chemical Name:1-(6-(6-(2-(2,5-difluorophenyl)pyrrolidin-1-yl)imidazo[1,2-b]pyridazin-3-yl)pyridin-2-yl)piperidin-4-ol
CAS No.:1196546-70-9
Molecular Formula:C₂₉H₂₉F₂N₇O
Molecular Weight:529.592
Hs Code.:

Synonyms:1-(6-(6-(2-(2,5-difluorophenyl)pyrrolidin-1-yl)imidazo[1,2-b]pyridazin-3-yl)pyridin-2-yl)piperidin-4-ol

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Chemical Property of 1-(6-(6-(2-(2,5-difluorophenyl)pyrrolidin-1-yl)imidazo[1,2-b]pyridazin-3-yl)pyridin-2-yl)piperidin-4-ol

Chemical Property:

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Technology Process of 1-(6-(6-(2-(2,5-difluorophenyl)pyrrolidin-1-yl)imidazo[1,2-b]pyridazin-3-yl)pyridin-2-yl)piperidin-4-ol

There total 9 articles about 1-(6-(6-(2-(2,5-difluorophenyl)pyrrolidin-1-yl)imidazo[1,2-b]pyridazin-3-yl)pyridin-2-yl)piperidin-4-ol 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:

: 2038-03-1
4-(2-AMINOETHYL)MORPHOLINE

: 1196546-61-8
4-(6-(2-(2,5-difluorophenyl)pyrrolidin-1-yl)imidazo[1,2-b]pyridazin-3-yl)-2-fluorobenzonitrile

: 1196546-70-9
1-(6-(6-(2-(2,5-difluorophenyl)pyrrolidin-1-yl)imidazo[1,2-b]pyridazin-3-yl)pyridin-2-yl)piperidin-4-ol

Guidance literature:: In N,N-dimethyl-formamide; at 110 ℃; for 12h;

Reference yield:

: (2,5-difluorophenyl)magnesium chloride

: 1196546-70-9
1-(6-(6-(2-(2,5-difluorophenyl)pyrrolidin-1-yl)imidazo[1,2-b]pyridazin-3-yl)pyridin-2-yl)piperidin-4-ol

Guidance literature:: Multi-step reaction with 6 steps

1.1: tetrahydrofuran / 1 h / -78 °C / Inert atmosphere

1.2: 20 °C

2.1: hydrogenchloride; water / methanol / 6 h / 70 °C

3.1: sodium tetrahydroborate / ethanol / 20 °C

4.1: potassium fluoride / dimethyl sulfoxide / 130 °C

5.1: water; sodium carbonate / (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride / 1,4-dioxane / 0.2 h / 150 °C / Microwave irradiation

6.1: N,N-dimethyl-formamide / 12 h / 110 °C

With hydrogenchloride; potassium fluoride; sodium tetrahydroborate; water; sodium carbonate; (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; In tetrahydrofuran; 1,4-dioxane; methanol; ethanol; dimethyl sulfoxide; N,N-dimethyl-formamide;

Reference yield:

: 399-94-0
2-bromo-1,4-difluorobenzene

: 1196546-70-9
1-(6-(6-(2-(2,5-difluorophenyl)pyrrolidin-1-yl)imidazo[1,2-b]pyridazin-3-yl)pyridin-2-yl)piperidin-4-ol

Guidance literature:: Multi-step reaction with 7 steps

1.1: isopropylmagnesium chloride / tetrahydrofuran / 0.5 h / -78 - -20 °C / Inert atmosphere

2.1: tetrahydrofuran / 1 h / -78 °C / Inert atmosphere

2.2: 20 °C

3.1: hydrogenchloride; water / methanol / 6 h / 70 °C

4.1: sodium tetrahydroborate / ethanol / 20 °C

5.1: potassium fluoride / dimethyl sulfoxide / 130 °C

6.1: water; sodium carbonate / (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride / 1,4-dioxane / 0.2 h / 150 °C / Microwave irradiation

7.1: N,N-dimethyl-formamide / 12 h / 110 °C

With hydrogenchloride; potassium fluoride; sodium tetrahydroborate; water; isopropylmagnesium chloride; sodium carbonate; (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; In tetrahydrofuran; 1,4-dioxane; methanol; ethanol; dimethyl sulfoxide; N,N-dimethyl-formamide;