tert-butyl 4-(5-(2-aminoimidazo[1,2-b]pyridazin-6-yl)-4-(4-fluorophenyl)-1H-imidazol-1-yl)piperidine-1-carboxylate

Base Information

Chemical Name:tert-butyl 4-(5-(2-aminoimidazo[1,2-b]pyridazin-6-yl)-4-(4-fluorophenyl)-1H-imidazol-1-yl)piperidine-1-carboxylate
CAS No.:1615729-99-1
Molecular Formula:C₂₅H₂₈FN₇O₂
Molecular Weight:477.541
Hs Code.:

Synonyms:tert-butyl 4-(5-(2-aminoimidazo[1,2-b]pyridazin-6-yl)-4-(4-fluorophenyl)-1H-imidazol-1-yl)piperidine-1-carboxylate

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Chemical Property of tert-butyl 4-(5-(2-aminoimidazo[1,2-b]pyridazin-6-yl)-4-(4-fluorophenyl)-1H-imidazol-1-yl)piperidine-1-carboxylate

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Technology Process of tert-butyl 4-(5-(2-aminoimidazo[1,2-b]pyridazin-6-yl)-4-(4-fluorophenyl)-1H-imidazol-1-yl)piperidine-1-carboxylate

There total 9 articles about tert-butyl 4-(5-(2-aminoimidazo[1,2-b]pyridazin-6-yl)-4-(4-fluorophenyl)-1H-imidazol-1-yl)piperidine-1-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: 95.0%

: 24424-99-5
di-tert-butyl dicarbonate

: 1615729-97-9
6-(4-(4-fluorophenyl)-1-(piperidin-4-yl)-1H-imidazol-5-yl)imidazo[1,2-b]pyridazin-2-amine

: 1615729-99-1
tert-butyl 4-(5-(2-aminoimidazo[1,2-b]pyridazin-6-yl)-4-(4-fluorophenyl)-1H-imidazol-1-yl)piperidine-1-carboxylate

Guidance literature:: With dmap; In dichloromethane; at 20 ℃; for 0.75h;

Reference yield:

: 109384-19-2
t-butyl 4-hydroxy piperidine-1-carboxylate

: 1615729-99-1
tert-butyl 4-(5-(2-aminoimidazo[1,2-b]pyridazin-6-yl)-4-(4-fluorophenyl)-1H-imidazol-1-yl)piperidine-1-carboxylate

Guidance literature:: Multi-step reaction with 6 steps

1.1: triethylamine / dichloromethane / 1 h / 0 - 20 °C

2.1: sodium hydride / 1-methyl-pyrrolidin-2-one; mineral oil / 0.75 h / 20 °C

2.2: 16.33 h / 80 °C

3.1: N-Bromosuccinimide / dichloromethane / 0.67 h / 20 °C

4.1: potassium phosphate; dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH₂Cl₂ / 1,4-dioxane; water / 16 h / 80 °C / Inert atmosphere

5.1: hydrogenchloride / 1,4-dioxane; methanol / 16 h / 20 °C

6.1: dmap / dichloromethane / 0.75 h / 20 °C

With hydrogenchloride; dmap; potassium phosphate; N-Bromosuccinimide; dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH₂Cl₂; sodium hydride; triethylamine; In 1,4-dioxane; 1-methyl-pyrrolidin-2-one; methanol; dichloromethane; water; mineral oil;

Reference yield:

: 1615729-70-8
tert-butyl 4-(4-(4-fluorophenyl)-1H-imidazol-1-yl)piperidine-1-carboxylate

: 1615729-99-1
tert-butyl 4-(5-(2-aminoimidazo[1,2-b]pyridazin-6-yl)-4-(4-fluorophenyl)-1H-imidazol-1-yl)piperidine-1-carboxylate

Guidance literature:: Multi-step reaction with 4 steps

1: N-Bromosuccinimide / dichloromethane / 0.67 h / 20 °C

2: potassium phosphate; dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH₂Cl₂ / 1,4-dioxane; water / 16 h / 80 °C / Inert atmosphere

3: hydrogenchloride / 1,4-dioxane; methanol / 16 h / 20 °C

4: dmap / dichloromethane / 0.75 h / 20 °C

With hydrogenchloride; dmap; potassium phosphate; N-Bromosuccinimide; dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH₂Cl₂; In 1,4-dioxane; methanol; dichloromethane; water;