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5-(6-(4-(3-aminomethyloxetan-3-ylmethoxy)phenyl)imidazo[1,2-b]pyridazin-3-yl)-3-trifluoromethylpyridin-2-ylamine

Base Information
  • Chemical Name:5-(6-(4-(3-aminomethyloxetan-3-ylmethoxy)phenyl)imidazo[1,2-b]pyridazin-3-yl)-3-trifluoromethylpyridin-2-ylamine
  • CAS No.:1084952-83-9
  • Molecular Formula:C23H21F3N6O2
  • Molecular Weight:470.454
  • Hs Code.:
5-(6-(4-(3-aminomethyloxetan-3-ylmethoxy)phenyl)imidazo[1,2-b]pyridazin-3-yl)-3-trifluoromethylpyridin-2-ylamine

Synonyms:5-(6-(4-(3-aminomethyloxetan-3-ylmethoxy)phenyl)imidazo[1,2-b]pyridazin-3-yl)-3-trifluoromethylpyridin-2-ylamine

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Chemical Property of 5-(6-(4-(3-aminomethyloxetan-3-ylmethoxy)phenyl)imidazo[1,2-b]pyridazin-3-yl)-3-trifluoromethylpyridin-2-ylamine
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Technology Process of 5-(6-(4-(3-aminomethyloxetan-3-ylmethoxy)phenyl)imidazo[1,2-b]pyridazin-3-yl)-3-trifluoromethylpyridin-2-ylamine

There total 8 articles about 5-(6-(4-(3-aminomethyloxetan-3-ylmethoxy)phenyl)imidazo[1,2-b]pyridazin-3-yl)-3-trifluoromethylpyridin-2-ylamine 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:
Guidance literature:
With hydrogen; palladium 10% on activated carbon; In tetrahydrofuran; methanol; N,N-dimethyl-formamide; at 20 ℃; for 48h; under 3750.38 Torr;
Guidance literature:
Multi-step reaction with 7 steps
1: di-isopropyl azodicarboxylate; triphenylphosphine / tetrahydrofuran / 5 h / 20 °C
2: triethylamine / dichloromethane / 1 h / 10 - 20 °C
3: ammonia / methanol / 144 h
4: sodium carbonate / dichloromethane; water / 1 h / 20 °C
5: potassium acetate / bis-triphenylphosphine-palladium(II) chloride / N,N-dimethyl-formamide / 16 h / 95 °C
6: potassium carbonate / (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride / ethanol; toluene / 6 h / Heating / reflux
7: hydrogen / palladium 10% on activated carbon / tetrahydrofuran; methanol; N,N-dimethyl-formamide / 48 h / 20 °C / 3750.38 Torr
With di-isopropyl azodicarboxylate; ammonia; hydrogen; potassium acetate; sodium carbonate; potassium carbonate; triethylamine; triphenylphosphine; bis-triphenylphosphine-palladium(II) chloride; (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; palladium 10% on activated carbon; In tetrahydrofuran; methanol; ethanol; dichloromethane; water; N,N-dimethyl-formamide; toluene;
Guidance literature:
Multi-step reaction with 8 steps
1: potassium hydroxide; Diethyl carbonate / ethanol / 4 h / Heating / reflux
2: di-isopropyl azodicarboxylate; triphenylphosphine / tetrahydrofuran / 5 h / 20 °C
3: triethylamine / dichloromethane / 1 h / 10 - 20 °C
4: ammonia / methanol / 144 h
5: sodium carbonate / dichloromethane; water / 1 h / 20 °C
6: potassium acetate / bis-triphenylphosphine-palladium(II) chloride / N,N-dimethyl-formamide / 16 h / 95 °C
7: potassium carbonate / (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride / ethanol; toluene / 6 h / Heating / reflux
8: hydrogen / palladium 10% on activated carbon / tetrahydrofuran; methanol; N,N-dimethyl-formamide / 48 h / 20 °C / 3750.38 Torr
With potassium hydroxide; di-isopropyl azodicarboxylate; ammonia; hydrogen; potassium acetate; sodium carbonate; potassium carbonate; triethylamine; triphenylphosphine; Diethyl carbonate; bis-triphenylphosphine-palladium(II) chloride; (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; palladium 10% on activated carbon; In tetrahydrofuran; methanol; ethanol; dichloromethane; water; N,N-dimethyl-formamide; toluene;
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