Multi-step reaction with 10 steps
1.1: chloro-trimethyl-silane / 20 h / 0 - 20 °C
2.1: N-ethyl-N,N-diisopropylamine; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; benzotriazol-1-ol / N,N-dimethyl-formamide / 16 h / 0 - 20 °C
3.1: 2,3-dicyano-5,6-dichloro-p-benzoquinone / tetrahydrofuran / 1 h / 85 °C
4.1: hydrogen / palladium 10% on activated carbon / methanol / 1 h
5.1: 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; benzotriazol-1-ol / N,N-dimethyl-formamide / 16 h / 0 - 20 °C
6.1: potassium carbonate; N,N,N,N-tetraethylammonium tetrafluoroborate / N,N-dimethyl-formamide; water / 72 h / Electrochemical reaction
7.1: water; lithium hydroxide / methanol / 18 h / 20 °C / Cooling with ice
7.2: 10 °C
8.1: N-ethyl-N,N-diisopropylamine; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; benzotriazol-1-ol / N,N-dimethyl-formamide / 16 h / 0 - 20 °C
9.1: (bis-(2-methoxyethyl)amino)sulfur trufluoride / dichloromethane / -20 - 20 °C
10.1: Bromotrichloromethane; 1,8-diazabicyclo[5.4.0]undec-7-ene / dichloromethane / 0 - 20 °C
With
chloro-trimethyl-silane; Bromotrichloromethane; water; hydrogen; N,N,N,N-tetraethylammonium tetrafluoroborate; potassium carbonate; benzotriazol-1-ol; 1,8-diazabicyclo[5.4.0]undec-7-ene; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine; 2,3-dicyano-5,6-dichloro-p-benzoquinone; lithium hydroxide; (bis-(2-methoxyethyl)amino)sulfur trufluoride;
palladium 10% on activated carbon;
In
tetrahydrofuran; methanol; dichloromethane; water; N,N-dimethyl-formamide;