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1-benzyl-N,N-dimethyl-4-(3-(2-(pyridin-4-yl)ethyl)-1H-indol-2-yl)cyclohexanamine citrate

Base Information Edit
  • Chemical Name:1-benzyl-N,N-dimethyl-4-(3-(2-(pyridin-4-yl)ethyl)-1H-indol-2-yl)cyclohexanamine citrate
  • CAS No.:1004543-96-7
  • Molecular Formula:C6H8O7*C30H35N3
  • Molecular Weight:629.753
  • Hs Code.:
  • Mol file:1004543-96-7.mol
1-benzyl-N,N-dimethyl-4-(3-(2-(pyridin-4-yl)ethyl)-1H-indol-2-yl)cyclohexanamine citrate

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Chemical Property of 1-benzyl-N,N-dimethyl-4-(3-(2-(pyridin-4-yl)ethyl)-1H-indol-2-yl)cyclohexanamine citrate Edit
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Technology Process of 1-benzyl-N,N-dimethyl-4-(3-(2-(pyridin-4-yl)ethyl)-1H-indol-2-yl)cyclohexanamine citrate

There total 4 articles about 1-benzyl-N,N-dimethyl-4-(3-(2-(pyridin-4-yl)ethyl)-1H-indol-2-yl)cyclohexanamine citrate 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 3 steps
1.1: trifluorormethanesulfonic acid / dichloromethane / 67 h / 20 °C
1.2: 1 h
2.1: hydrogen / 5%-palladium/activated carbon / methanol / 3 h / 20 °C / 2250.23 Torr / Inert atmosphere
3.1: methanol; chloroform
With trifluorormethanesulfonic acid; hydrogen; 5%-palladium/activated carbon; In methanol; dichloromethane; chloroform;
Guidance literature:
Multi-step reaction with 3 steps
1.1: trifluorormethanesulfonic acid / dichloromethane / 67 h / 20 °C
1.2: 1 h
2.1: hydrogen / 5%-palladium/activated carbon / methanol / 3 h / 20 °C / 2250.23 Torr / Inert atmosphere
3.1: methanol; chloroform
With trifluorormethanesulfonic acid; hydrogen; 5%-palladium/activated carbon; In methanol; dichloromethane; chloroform;
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