Multi-step reaction with 13 steps
1.1: trichlorophosphate / 0.17 h / 0 - 20 °C
1.2: 2 h / 50 °C / Heating / reflux
1.3: 0.5 h / Heating / reflux
2.1: toluene / 100 °C
3.1: sodium tetrahydroborate / methanol / 1 h / 20 °C
4.1: trifluoroacetic acid / dichloromethane / 20 °C
5.1: Resolution of racemate
6.1: lithium aluminium tetrahydride / tetrahydrofuran / 3 h / 0 °C
6.2: 3 h / 0 °C
7.1: triethylamine / dichloromethane / 3 h / 0 °C
8.1: dimethyl sulfoxide / 13 h / 50 °C
9.1: sodium hydroxide; water; isopropyl alcohol / 96 h / Heating / reflux
9.2: 0 °C
10.1: benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / dichloromethane / 20 °C
11.1: trimethylsilylazide; triphenylphosphine; diethylazodicarboxylate / tetrahydrofuran; toluene / 20 °C
12.1: 1,8-diazabicyclo[5.4.0]undec-7-ene / dichloromethane / 20 °C
13.1: potassium carbonate / N,N-dimethyl-formamide / 20 °C
With
sodium hydroxide; sodium tetrahydroborate; lithium aluminium tetrahydride; trimethylsilylazide; water; potassium carbonate; benzotriazol-1-ol; 1,8-diazabicyclo[5.4.0]undec-7-ene; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; triphenylphosphine; isopropyl alcohol; trifluoroacetic acid; diethylazodicarboxylate; trichlorophosphate;
In
tetrahydrofuran; methanol; dichloromethane; dimethyl sulfoxide; N,N-dimethyl-formamide; toluene;
11.1: Mitsunobu reaction;