Technology Process of 4-[(10-allyl-9,10-diazatricyclo[4.2.1.1(2,5)]dec-9-yl)-(3-hydroxyphenyl)methyl]-N,N-diethylbenzamide
There total 17 articles about 4-[(10-allyl-9,10-diazatricyclo[4.2.1.1(2,5)]dec-9-yl)-(3-hydroxyphenyl)methyl]-N,N-diethylbenzamide 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:
-
4-[(10-allyl-9,10-diazatricyclo[4.2.1.1(2,5)]dec-9-yl)-(3-methoxyphenyl)methyl]-N,N-diethylbenzamide;
With
boron tribromide;
In
dichloromethane;
at 0 ℃;
for 1.5h;
With
potassium hydroxide;
In
dichloromethane; water;
- Guidance literature:
-
Multi-step reaction with 9 steps
1.1: aluminum (III) chloride / dichloromethane / 4 h / 20 °C
2.1: potassium permanganate / water; tert-butyl alcohol / 7.5 h / Reflux
3.1: 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; benzotriazol-1-ol / dichloromethane / 0.5 h / 20 °C
3.2: 14 h / 20 °C
4.1: sodium tetrahydroborate / ethanol; water / 2 h / 20 °C
4.2: pH 5
5.1: hydrogenchloride / chloroform; water / 14 h / 20 °C
6.1: potassium carbonate / acetonitrile / 72 h / Reflux
7.1: hydrogen / palladium 10% on activated carbon / ethanol / 6 h / 60 °C / 2327.23 Torr
8.1: potassium carbonate / acetone / 14 h / Reflux
9.1: boron tribromide / dichloromethane / 1.5 h / 0 °C
With
hydrogenchloride; aluminum (III) chloride; sodium tetrahydroborate; potassium permanganate; hydrogen; boron tribromide; potassium carbonate; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride;
palladium 10% on activated carbon;
In
ethanol; dichloromethane; chloroform; water; acetone; acetonitrile; tert-butyl alcohol;
- Guidance literature:
-
Multi-step reaction with 10 steps
1.1: sodium carbonate / dichloromethane / 0 °C
1.2: 16 h / 20 °C
2.1: ytterbium(III) triflate / tetrahydrofuran / 20 h / Reflux
3.1: triethylamine; methanesulfonyl chloride / dmap / dichloromethane / 14 h / 0 - 20 °C / Inert atmosphere
4.1: sodium azide; ammonium chloride / ethanol; water / 4 h / Reflux
5.1: bromine / cyclohexane; water / 5 h / 20 °C
6.1: triphenylphosphine / water; tetrahydrofuran / 19 h / 20 °C / Reflux
6.2: pH 8
7.1: potassium carbonate / acetonitrile / 72 h / Reflux
8.1: hydrogen / palladium 10% on activated carbon / ethanol / 6 h / 60 °C / 2327.23 Torr
9.1: potassium carbonate / acetone / 14 h / Reflux
10.1: boron tribromide / dichloromethane / 1.5 h / 0 °C
With
sodium azide; hydrogen; bromine; boron tribromide; sodium carbonate; potassium carbonate; ammonium chloride; methanesulfonyl chloride; triethylamine; triphenylphosphine; ytterbium(III) triflate;
dmap; palladium 10% on activated carbon;
In
tetrahydrofuran; ethanol; dichloromethane; cyclohexane; water; acetone; acetonitrile;