Technology Process of iso-propyl-9-anilinoacridine-4-carboxylate
There total 4 articles about iso-propyl-9-anilinoacridine-4-carboxylate 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:
-
1,2,4-Triazole;
With
triethylamine; trichlorophosphate;
In
acetonitrile;
at 0 ℃;
for 0.5h;
9-oxo-9,10-dihydro-acridine-4-carboxylic acid isopropyl ester;
In
dichloromethane; acetonitrile;
for 96h;
Heating;
aniline;
With
TEA;
In
acetonitrile;
for 24h;
Further stages.;
Heating;
DOI:10.1021/ol005809v
- Guidance literature:
-
Multi-step reaction with 2 steps
1.1: 95 percent / carbonyldiimidazole / tetrahydrofuran / 6 h / 20 °C
2.1: phosphoryl chloride; triethylamine / acetonitrile / 0.5 h / 0 °C
2.2: acetonitrile; CH2Cl2 / 96 h / Heating
2.3: 0.155 g / TEA / acetonitrile / 24 h / Heating
With
triethylamine; 1,1'-carbonyldiimidazole; trichlorophosphate;
In
tetrahydrofuran; acetonitrile;
1.1: Esterification / 2.1: Substitution / 2.2: Substitution / 2.3: Substitution;
DOI:10.1021/ol005809v
- Guidance literature:
-
Multi-step reaction with 3 steps
2.1: 95 percent / carbonyldiimidazole / tetrahydrofuran / 6 h / 20 °C
3.1: phosphoryl chloride; triethylamine / acetonitrile / 0.5 h / 0 °C
3.2: acetonitrile; CH2Cl2 / 96 h / Heating
3.3: 0.155 g / TEA / acetonitrile / 24 h / Heating
With
triethylamine; 1,1'-carbonyldiimidazole; trichlorophosphate;
In
tetrahydrofuran; acetonitrile;
1.1: Cyclocondensation / 2.1: Esterification / 3.1: Substitution / 3.2: Substitution / 3.3: Substitution;
DOI:10.1021/ol005809v
