Multi-step reaction with 9 steps
1.1: dmap; N-ethyl-N,N-diisopropylamine / tetrahydrofuran / 2 h / 65 °C
2.1: oxalyl dichloride / N,N-dimethyl-formamide / dichloromethane / 6 h / 0 - 20 °C
3.1: N-ethyl-N,N-diisopropylamine / dichloromethane / 0 °C
3.2: 72 h / 20 °C
4.1: lithium aluminium tetrahydride / tetrahydrofuran / 72 h / -10 - 20 °C
4.2: 0 °C
5.1: ammonium acetate / 3 h / 120 °C
6.1: lithium aluminium tetrahydride / tetrahydrofuran / 16 h / 5 - 20 °C
7.1: triethylamine / dichloromethane / 16 h / 20 °C
8.1: dmap; N-ethyl-N,N-diisopropylamine; 2,6-Dichlorobenzoyl chloride / dichloromethane / 16 h / 20 °C
9.1: tetrabutyl ammonium fluoride / tetrahydrofuran / 24 h
With
dmap; lithium aluminium tetrahydride; oxalyl dichloride; ammonium acetate; tetrabutyl ammonium fluoride; triethylamine; N-ethyl-N,N-diisopropylamine; 2,6-Dichlorobenzoyl chloride;
N,N-dimethyl-formamide;
In
tetrahydrofuran; dichloromethane;