Technology Process of 1-Isoquinolinecarboxaldehyde, 3-phenyl-
There total 12 articles about 1-Isoquinolinecarboxaldehyde, 3-phenyl- 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
selenium(IV) oxide;
In
1,4-dioxane;
at 102 ℃;
for 3h;
Schlenk technique;
Sealed tube;
DOI:10.1021/acs.orglett.1c01237
- Guidance literature:
-
With
sulfur trioxide pyridine complex; triethylamine;
In
dimethyl sulfoxide;
at 20 ℃;
for 10h;
DOI:10.1016/j.tetlet.2019.151287
- Guidance literature:
-
Multi-step reaction with 4 steps
1: ammonium hydroxide / water; acetonitrile / 12 h / 70 °C
2: pyridine / dichloromethane / 1 h / 0 °C
3: methanesulfonic acid(2-dicyclohexylphosphino-2′,4′,6′-triisopropyl-1,1′-biphenyl)[2-(2′-amino-1,1′-biphenyl)]palladium(II); potassium phosphate / tetrahydrofuran / 2 h / 40 °C
4: selenium(IV) oxide / 1,4-dioxane / 2 h / 110 °C
With
pyridine; selenium(IV) oxide; ammonium hydroxide; potassium phosphate; methanesulfonic acid(2-dicyclohexylphosphino-2′,4′,6′-triisopropyl-1,1′-biphenyl)[2-(2′-amino-1,1′-biphenyl)]palladium(II);
In
tetrahydrofuran; 1,4-dioxane; dichloromethane; water; acetonitrile;
3: |Suzuki Coupling;
DOI:10.1021/acscatal.0c00211