Technology Process of 3-(4-Chloro-phenyl)-2-(4-methoxy-phenylamino)-7-methyl-3H-1,3,4-triaza-phenalene-5-carboxylic acid ethyl ester
There total 7 articles about 3-(4-Chloro-phenyl)-2-(4-methoxy-phenylamino)-7-methyl-3H-1,3,4-triaza-phenalene-5-carboxylic acid ethyl ester 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:
-
Multi-step reaction with 8 steps
1: H2 / 10percent Pd/C
2: LiAlH4
3: 2) sodium azide
4: pyridinium chlorochromate
6: triphenylphosphine
7: CH2Cl2 / 5 h / Ambient temperature; other heterocumulenes
8: toluene / 1) r.t., 30 min, 2) 170 deg C, 24 h
With
lithium aluminium tetrahydride; sodium azide; hydrogen; triphenylphosphine; pyridinium chlorochromate;
palladium on activated charcoal;
In
dichloromethane; toluene;
DOI:10.1016/S0040-4039(00)92391-8
- Guidance literature:
-
Multi-step reaction with 6 steps
1: 1) H2SO4, NaNO2, 2) NaN3 / 1) H2O, 0 deg C, 30 min, 2) 3 h
2: pyridinium chlorochromate / CH2Cl2 / 4 h / Ambient temperature
3: 67 percent / Na, EtOH / 5 h / -15 °C
4: 91 percent / diethyl ether / 12 h / Ambient temperature
5: 83 percent / CH2Cl2 / Ambient temperature; 1 equiv of isocyanate (reaction with 2 equiv of isocyanate, toluene, r.t., 1 h, then 160 deg, 1h leads directly to pyrido<2,3,4-de>quinazolines); sequential treatment with isocyanate and ketene or aldehydes and isocyanates; reaction with CS2
6: toluene / 1) room temperature, 1 h, 2) 160 deg C, 24 h
With
sodium azide; ethanol; sulfuric acid; sodium; pyridinium chlorochromate; sodium nitrite;
In
diethyl ether; dichloromethane; toluene;
DOI:10.1021/jo00051a007
- Guidance literature:
-
Multi-step reaction with 4 steps
1: 67 percent / Na, EtOH / 5 h / -15 °C
2: 91 percent / diethyl ether / 12 h / Ambient temperature
3: 83 percent / CH2Cl2 / Ambient temperature; 1 equiv of isocyanate (reaction with 2 equiv of isocyanate, toluene, r.t., 1 h, then 160 deg, 1h leads directly to pyrido<2,3,4-de>quinazolines); sequential treatment with isocyanate and ketene or aldehydes and isocyanates; reaction with CS2
4: toluene / 1) room temperature, 1 h, 2) 160 deg C, 24 h
With
ethanol; sodium;
In
diethyl ether; dichloromethane; toluene;
DOI:10.1021/jo00051a007