Technology Process of (E)-1-(3-(1,7-dimethyl-2-oxo-1,2-dihydro-1,6-naphthyridin-3-yl)-4-methylphenyl)-2-hydroxyguanidine
There total 16 articles about (E)-1-(3-(1,7-dimethyl-2-oxo-1,2-dihydro-1,6-naphthyridin-3-yl)-4-methylphenyl)-2-hydroxyguanidine which
guide to synthetic route it.
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synthetic route:
- Guidance literature:
-
With
hydroxylamine;
In
ethanol; water;
at 20 ℃;
for 12h;
- Guidance literature:
-
Multi-step reaction with 7 steps
1.1: water; potassium hydroxide / methanol / 14 h / Reflux
2.1: hydrogenchloride / 1,4-dioxane / 14 h / Reflux
2.2: pH > 12
3.1: hydrogen / palladium 10% on activated carbon / ethanol / 16 h / 20 °C
4.1: potassium carbonate / N,N-dimethyl-formamide / 16 h / 100 °C
5.1: tris-(dibenzylideneacetone)dipalladium(0); triphenylphosphine / 1,4-dioxane; toluene / 0.17 h / 150 °C / Microwave irradiation
6.1: potassium acetate / methanol / 0 - 20 °C
7.1: hydroxylamine / ethanol; water / 12 h / 20 °C
With
hydrogenchloride; water; hydrogen; hydroxylamine; potassium acetate; potassium carbonate; potassium hydroxide;
tris-(dibenzylideneacetone)dipalladium(0); palladium 10% on activated carbon; triphenylphosphine;
In
1,4-dioxane; methanol; ethanol; water; N,N-dimethyl-formamide; toluene;
- Guidance literature:
-
Multi-step reaction with 4 steps
1: potassium carbonate / N,N-dimethyl-formamide / 16 h / 100 °C
2: tris-(dibenzylideneacetone)dipalladium(0); triphenylphosphine / 1,4-dioxane; toluene / 0.17 h / 150 °C / Microwave irradiation
3: potassium acetate / methanol / 0 - 20 °C
4: hydroxylamine / ethanol; water / 12 h / 20 °C
With
hydroxylamine; potassium acetate; potassium carbonate;
tris-(dibenzylideneacetone)dipalladium(0); triphenylphosphine;
In
1,4-dioxane; methanol; ethanol; water; N,N-dimethyl-formamide; toluene;