Technology Process of C13H10N2O
There total 1 articles about C13H10N2O 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
potassium phosphate; copper(l) iodide; (S,S)-1,2-diaminocyclohexane;
In
1,4-dioxane;
at 110 ℃;
DOI:10.1016/j.bmcl.2011.06.112
- Guidance literature:
-
C13H10N2O;
With
bromine;
In
water; tert-butyl alcohol;
at 20 ℃;
With
palladium on activated charcoal; hydrogen;
In
ethanol;
at 20 ℃;
N,N-dimethyl-formamide;
Further stages;
DOI:10.1016/j.bmcl.2011.06.112
- Guidance literature:
-
Multi-step reaction with 4 steps
1.1: bromine / water; tert-butyl alcohol / 20 °C
1.2: 20 °C
2.1: sodium dihydrogenphosphate; sodium chlorite / tert-butyl alcohol / 20 °C
3.1: 4-methyl-morpholine; O-<[cyano(ethoxycarbonyl)methylene]amino>-1,1,3,3-tetramethyluronium tetrafluoroborate / N,N-dimethyl-formamide / 20 °C
4.1: 1-methyl-pyrrolidin-2-one; sodium hydride / 20 - 140 °C / Microwave irradiation
With
4-methyl-morpholine; 1-methyl-pyrrolidin-2-one; sodium chlorite; sodium dihydrogenphosphate; O-<[cyano(ethoxycarbonyl)methylene]amino>-1,1,3,3-tetramethyluronium tetrafluoroborate; bromine; sodium hydride;
In
water; N,N-dimethyl-formamide; tert-butyl alcohol;
1.1: Vilsmeier-Haack formylation;
DOI:10.1016/j.bmcl.2011.06.112