7-fluoro-1-(2-(4-(5-(trifluoromethyl)-1H-benzo[d]imidazol-2-yl)piperazin-1-yl)ethyl)-1,5-naphthyridin-2(1H)-one

Base Information

Chemical Name:7-fluoro-1-(2-(4-(5-(trifluoromethyl)-1H-benzo[d]imidazol-2-yl)piperazin-1-yl)ethyl)-1,5-naphthyridin-2(1H)-one
CAS No.:1613053-81-8
Molecular Formula:C₂₂H₂₀F₄N₆O
Molecular Weight:460.434
Hs Code.:

Synonyms:7-fluoro-1-(2-(4-(5-(trifluoromethyl)-1H-benzo[d]imidazol-2-yl)piperazin-1-yl)ethyl)-1,5-naphthyridin-2(1H)-one

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Chemical Property of 7-fluoro-1-(2-(4-(5-(trifluoromethyl)-1H-benzo[d]imidazol-2-yl)piperazin-1-yl)ethyl)-1,5-naphthyridin-2(1H)-one

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Technology Process of 7-fluoro-1-(2-(4-(5-(trifluoromethyl)-1H-benzo[d]imidazol-2-yl)piperazin-1-yl)ethyl)-1,5-naphthyridin-2(1H)-one

There total 1 articles about 7-fluoro-1-(2-(4-(5-(trifluoromethyl)-1H-benzo[d]imidazol-2-yl)piperazin-1-yl)ethyl)-1,5-naphthyridin-2(1H)-one 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:

: 884495-03-8
3-amino-2-bromo-5-fluoropyridine

: 1613053-81-8
7-fluoro-1-(2-(4-(5-(trifluoromethyl)-1H-benzo[d]imidazol-2-yl)piperazin-1-yl)ethyl)-1,5-naphthyridin-2(1H)-one

Guidance literature:: Multi-step reaction with 6 steps

1.1: palladium diacetate; tri-tert-butyl phosphine; N-Methyldicyclohexylamine; Isopropylbenzene / 150 °C

2.1: caesium carbonate / dimethyl sulfoxide / 0.17 h / 20 °C

2.2: 20 - 90 °C

3.1: triethylamine / dichloromethane / 0.5 h / 0 °C / Inert atmosphere

4.1: sodium carbonate / N,N-dimethyl-formamide / 3 h / 92 °C

5.1: hydrogenchloride / 1,4-dioxane / 2 h / 80 °C

6.1: N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide / 2 h / 130 °C / Microwave irradiation

With hydrogenchloride; Isopropylbenzene; tri-tert-butyl phosphine; N-Methyldicyclohexylamine; palladium diacetate; sodium carbonate; caesium carbonate; triethylamine; N-ethyl-N,N-diisopropylamine; In 1,4-dioxane; dichloromethane; dimethyl sulfoxide; N,N-dimethyl-formamide;
DOI:10.1021/ml5001728

Reference yield: 24.0%

: 1576-43-8
4-hydroxybenzenesulphonamide

: 1613053-81-8
7-fluoro-1-(2-(4-(5-(trifluoromethyl)-1H-benzo[d]imidazol-2-yl)piperazin-1-yl)ethyl)-1,5-naphthyridin-2(1H)-one

: 1613053-94-3
4-((5-(2-(4-(5-cyano-1H-benzo[d]imidazol-2-yl)piperidin-1-yl)ethyl)-6-oxo-5,6-dihydro-1,5-naphthyridin-3-yl)oxy)benzenesulfonamide

Guidance literature:: 4-hydroxybenzenesulphonamide; With caesium carbonate; In dimethyl sulfoxide; at 20 ℃; for 0.5h;

7-fluoro-1-(2-(4-(5-(trifluoromethyl)-1H-benzo[d]imidazol-2-yl)piperazin-1-yl)ethyl)-1,5-naphthyridin-2(1H)-one; In dimethyl sulfoxide; at 120 ℃;
DOI:10.1021/ml5001728