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UN(107)C10957A

Base Information
  • Chemical Name:UN(107)C10957A
  • CAS No.:1354030-72-0
  • Molecular Formula:C23H30N4O3
  • Molecular Weight:410.516
  • Hs Code.:
UN<sup>(107)</sup>C<sub>10957</sub>A

Synonyms:UN(107)C10957A

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Chemical Property of UN(107)C10957A
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Technology Process of UN(107)C10957A

There total 11 articles about UN(107)C10957A 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:
4-(7-oxo-5,6,7,8-tetrahydro-1,8-naphthyridin-2-yloxy)butyl methanesulfonate; With sodium iodide; In acetonitrile; for 0.5h; Reflux;
1-(2-methoxyphenyl)piperazine hydrochloride; With potassium carbonate; In acetonitrile; for 4h; Reflux;
Guidance literature:
Multi-step reaction with 9 steps
1.1: triethylamine / dichloromethane / 20 °C / Cooling with ice
2.1: n-butyllithium / tetrahydrofuran / 3 h / -20 °C
2.2: -20 - 20 °C
3.1: sodium hydride / N,N-dimethyl-formamide / 0.33 h / 0 °C
4.1: sodium hydride / tetrahydrofuran / Inert atmosphere; Cooling with ice
4.2: Reflux
5.1: hydrogen / Raney nickel / tetrahydrofuran
6.1: hydrogenchloride / 1,4-dioxane / 3 h / Reflux
6.2: 20 °C / pH 8
7.1: hydrogen / palladium 10% on activated carbon / ethanol
8.1: triethylamine / dichloromethane / 6 h / 20 °C
9.1: sodium iodide / acetonitrile / 0.5 h / Reflux
9.2: 4 h / Reflux
With hydrogenchloride; n-butyllithium; hydrogen; sodium hydride; triethylamine; sodium iodide; palladium 10% on activated carbon; In tetrahydrofuran; 1,4-dioxane; ethanol; dichloromethane; N,N-dimethyl-formamide; acetonitrile;
Guidance literature:
Multi-step reaction with 8 steps
1.1: n-butyllithium / tetrahydrofuran / 3 h / -20 °C
1.2: -20 - 20 °C
2.1: sodium hydride / N,N-dimethyl-formamide / 0.33 h / 0 °C
3.1: sodium hydride / tetrahydrofuran / Inert atmosphere; Cooling with ice
3.2: Reflux
4.1: hydrogen / Raney nickel / tetrahydrofuran
5.1: hydrogenchloride / 1,4-dioxane / 3 h / Reflux
5.2: 20 °C / pH 8
6.1: hydrogen / palladium 10% on activated carbon / ethanol
7.1: triethylamine / dichloromethane / 6 h / 20 °C
8.1: sodium iodide / acetonitrile / 0.5 h / Reflux
8.2: 4 h / Reflux
With hydrogenchloride; n-butyllithium; hydrogen; sodium hydride; triethylamine; sodium iodide; palladium 10% on activated carbon; In tetrahydrofuran; 1,4-dioxane; ethanol; dichloromethane; N,N-dimethyl-formamide; acetonitrile;
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