Technology Process of 1-(3,3-diphenylpropyl)-3-(3-hydroxymethylphenyl)-1-(2-morpholin-4-ylethyl)urea
There total 10 articles about 1-(3,3-diphenylpropyl)-3-(3-hydroxymethylphenyl)-1-(2-morpholin-4-ylethyl)urea 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:
-
3-[3-(3,3-diphenylpropyl)-3-(2-morpholin-4-ylethyl)ureido]benzoic acid methyl ester;
With
diisobutylaluminium hydride;
In
tetrahydrofuran; dichloromethane;
at -78 - -27 ℃;
With
lithium aluminium tetrahydride;
In
tetrahydrofuran; dichloromethane;
at -78 - 0 ℃;
for 1.5h;
With
water; sodium tartrate; potassium tartrate;
In
tetrahydrofuran; dichloromethane;
at 0 - 20 ℃;
for 1h;
- Guidance literature:
-
Multi-step reaction with 3 steps
1.1: hydrogen / palladium 10% on activated carbon / ethanol / 16 h / 20 °C / 760.05 Torr
2.1: dichloromethane / 2 h / 20 °C
3.1: diisobutylaluminium hydride / tetrahydrofuran; dichloromethane / -78 - -27 °C
3.2: 1.5 h / -78 - 0 °C
3.3: 1 h / 0 - 20 °C
With
hydrogen; diisobutylaluminium hydride;
palladium 10% on activated carbon;
In
tetrahydrofuran; ethanol; dichloromethane;
- Guidance literature:
-
Multi-step reaction with 4 steps
1.1: Dess-Martin periodane / dichloromethane / 1.5 h / 0 °C
2.1: hydrogen / palladium 10% on activated carbon / ethanol / 16 h / 20 °C / 760.05 Torr
3.1: dichloromethane / 2 h / 20 °C
4.1: diisobutylaluminium hydride / tetrahydrofuran; dichloromethane / -78 - -27 °C
4.2: 1.5 h / -78 - 0 °C
4.3: 1 h / 0 - 20 °C
With
hydrogen; diisobutylaluminium hydride; Dess-Martin periodane;
palladium 10% on activated carbon;
In
tetrahydrofuran; ethanol; dichloromethane;