Technology Process of 2-(1-Benzyl-4-chloro-2,3-dihydro-1H-indol-5-yl)-1-methyl-ethylamine
There total 7 articles about 2-(1-Benzyl-4-chloro-2,3-dihydro-1H-indol-5-yl)-1-methyl-ethylamine 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
lithium aluminium tetrahydride;
In
tetrahydrofuran; diethyl ether;
for 2h;
Heating;
DOI:10.1021/jm00158a015
- Guidance literature:
-
Multi-step reaction with 4 steps
1: 93 percent / K2CO3, KI / dimethylformamide / 100 °C
2: 98 percent / POCl3 / H2O / 2 h / 100 °C
3: 81 percent / ammonium acetate / ethanol / 7 h / Heating
4: LiAlH4 / tetrahydrofuran; diethyl ether / 2 h / Heating
With
ammonium acetate; lithium aluminium tetrahydride; potassium carbonate; potassium iodide; trichlorophosphate;
In
tetrahydrofuran; diethyl ether; ethanol; water; N,N-dimethyl-formamide;
DOI:10.1021/jm00158a015
- Guidance literature:
-
Multi-step reaction with 7 steps
1: 71 percent / KOH / ethanol; dimethylsulfoxide / 72 h / Ambient temperature
2: 98 percent / Na2S*9H2O, sulfur / ethanol; H2O / 4 h / Heating
3: 78 percent / 4M HCl, SOCl2 / CHCl3; diethyl ether / 2 h / 50 °C
4: 93 percent / K2CO3, KI / dimethylformamide / 100 °C
5: 98 percent / POCl3 / H2O / 2 h / 100 °C
6: 81 percent / ammonium acetate / ethanol / 7 h / Heating
7: LiAlH4 / tetrahydrofuran; diethyl ether / 2 h / Heating
With
ammonium acetate; hydrogenchloride; sodium sulfide; potassium hydroxide; lithium aluminium tetrahydride; thionyl chloride; potassium carbonate; sulfur; potassium iodide; trichlorophosphate;
In
tetrahydrofuran; diethyl ether; ethanol; chloroform; water; dimethyl sulfoxide; N,N-dimethyl-formamide;
DOI:10.1021/jm00158a015