Multi-step reaction with 7 steps
1: 1.) N-methylmorpholine, isobutyl chloroformate / 1.) THF, -20 deg C, 15 min; 2.) -40 deg C -> room temp.
2: 100 percent / 1.) oxalyl chloride, DMSO; 2.) diisopropylethylamine / CH2Cl2 / 1.) -25 deg C, 1 h; 2.) -40 deg C -> room temp.
3: 39.2 percent / Zn / tetrahydrofuran / 4 h / Heating
4: 86.2 percent / ethanol / 1.) 4 h, reflux; 2.) room temp., 48 h,
5: 86.6 percent / H2 / 10percent Pd/C / ethanol / 2 h / 760 Torr
6: 41 percent / 1-ethyl-<3-(3-dimethylamino)propyl>carbodiimide hydrochloride, 1-hydroxybenzotriazole hydrate / CH2Cl2 / 24 h / Ambient temperature
7: 48 percent / Dess-Martin periodinane, CF3COOH / CH2Cl2 / Ambient temperature
With
4-methyl-morpholine; oxalyl dichloride; hydrogen; Dess-Martin periodane; dimethyl sulfoxide; 1-hydroxybenzotriazol-hydrate; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine; trifluoroacetic acid; zinc; isobutyl chloroformate;
palladium on activated charcoal;
In
tetrahydrofuran; ethanol; dichloromethane;
DOI:10.1021/ja00191a039