Technology Process of Cinnolin-8-amine
There total 10 articles about Cinnolin-8-amine which
guide to synthetic route it.
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synthetic route:
- Guidance literature:
-
With
titanium(III) chloride;
In
acetic acid;
at 11 ℃;
for 0.116667h;
- Guidance literature:
-
cinnoline-8-carboxylic acid;
With
diphenylphosphoranyl azide; triethylamine;
In
1,4-dioxane;
at 20 ℃;
for 1.33333h;
With
water;
In
1,4-dioxane;
at 100 ℃;
for 48h;
- Guidance literature:
-
Multi-step reaction with 8 steps
1.1: sulfuric acid / 16 h / 100 °C
2.1: sodium iodide; copper(l) iodide / 1,4-dioxane / 0.25 h / Sealed tube; Inert atmosphere
2.2: 16 h / 110 °C / Inert atmosphere
3.1: copper(l) iodide; triethylamine; bis-triphenylphosphine-palladium(II) chloride / acetonitrile / 3 h / 20 °C / Inert atmosphere
4.1: hydrogenchloride; sodium nitrite / water; tetrahydrofuran; acetonitrile / 0.25 h / -5 °C
4.2: 1.5 h / 0 - 20 °C
5.1: tetrabutyl ammonium fluoride / tetrahydrofuran / 3 h / 0 - 20 °C
6.1: 1,2-dichloro-benzene / 0.5 h / 200 °C / Sealed tube
7.1: lithium hydroxide monohydrate / tetrahydrofuran / 3 h / 20 °C
8.1: triethylamine; diphenylphosphoranyl azide / 1,4-dioxane / 1.33 h / 20 °C
8.2: 48 h / 100 °C
With
hydrogenchloride; bis-triphenylphosphine-palladium(II) chloride; copper(l) iodide; lithium hydroxide monohydrate; sulfuric acid; diphenylphosphoranyl azide; tetrabutyl ammonium fluoride; triethylamine; sodium iodide; sodium nitrite;
In
tetrahydrofuran; 1,4-dioxane; water; 1,2-dichloro-benzene; acetonitrile;