Technology Process of 6-[4-(2-nitroimidazol-1-ylmethyl)-1,2,3-triazol-1-yl]flavonol
There total 4 articles about 6-[4-(2-nitroimidazol-1-ylmethyl)-1,2,3-triazol-1-yl]flavonol 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
copper(II) sulfate; sodium L-ascorbate; tris[(1-benzyl-1H-1,2,3-triazol-4yl)methyl]amine;
In
water; dimethyl sulfoxide;
at 20 ℃;
DOI:10.1016/j.bmcl.2011.03.040
- Guidance literature:
-
Multi-step reaction with 4 steps
1.1: sulfuric acid; sodium nitrite / water / 0.5 h / 0 °C
1.2: 0 - 20 °C
2.1: sodium hydroxide / ethanol; water / 20 °C
3.1: dihydrogen peroxide; sodium hydroxide / ethanol; water / 20 °C / Cooling with ice
4.1: copper(II) sulfate; sodium L-ascorbate; tris[(1-benzyl-1H-1,2,3-triazol-4yl)methyl]amine / water; dimethyl sulfoxide / 20 °C
With
sulfuric acid; dihydrogen peroxide; copper(II) sulfate; sodium L-ascorbate; sodium hydroxide; sodium nitrite; tris[(1-benzyl-1H-1,2,3-triazol-4yl)methyl]amine;
In
ethanol; water; dimethyl sulfoxide;
2.1: Claisen-Schmidt condensation / 3.1: Algar-Flynn-Olyamada (AFO) reaction;
DOI:10.1016/j.bmcl.2011.03.040
- Guidance literature:
-
Multi-step reaction with 3 steps
1: sodium hydroxide / ethanol; water / 20 °C
2: dihydrogen peroxide; sodium hydroxide / ethanol; water / 20 °C / Cooling with ice
3: copper(II) sulfate; sodium L-ascorbate; tris[(1-benzyl-1H-1,2,3-triazol-4yl)methyl]amine / water; dimethyl sulfoxide / 20 °C
With
dihydrogen peroxide; copper(II) sulfate; sodium L-ascorbate; sodium hydroxide; tris[(1-benzyl-1H-1,2,3-triazol-4yl)methyl]amine;
In
ethanol; water; dimethyl sulfoxide;
1: Claisen-Schmidt condensation / 2: Algar-Flynn-Olyamada (AFO) reaction;
DOI:10.1016/j.bmcl.2011.03.040