Multi-step reaction with 11 steps
1.1: 94 percent / N,N-dimethylaminopyridine / acetonitrile / 15 h / 20 °C
2.1: aq. CsOH / methanol / 2 h / 20 °C
2.2: 79 percent / dimethylformamide / 18 h / 20 °C
3.1: DMSO; oxalyl chloride; NEtiPr2 / CH2Cl2 / -60 - 20 °C
4.1: CH2Cl2 / 20 h / 20 °C
5.1: 11.68 g / ammonium fluoride / methanol / 0.08 h
6.1: 90 percent / imidazole / dimethylformamide / 15 h / 20 °C
7.1: H2 / Pd/C / methanol; acetic acid / 15 h / 20 °C
8.1: 4.022 g / N,N-dimethylaminopyridine / toluene / 42 h / Heating
9.1: 100 percent / tetrabutylammonium fluoride / tetrahydrofuran / 1.5 h / 20 °C
10.1: 70 percent / Dess-Martin periodinane / CH2Cl2 / 1 h / 20 °C
11.1: 90 percent / NaH / tetrahydrofuran / 1.5 h
With
1H-imidazole; dmap; cesium hydroxide; ammonium fluoride; oxalyl dichloride; tetrabutyl ammonium fluoride; hydrogen; sodium hydride; Dess-Martin periodane; dimethyl sulfoxide; N-ethyl-N,N-diisopropylamine;
palladium on activated charcoal;
In
tetrahydrofuran; methanol; dichloromethane; acetic acid; N,N-dimethyl-formamide; toluene; acetonitrile;
3.1: Swern oxidation / 11.1: Horner-Wadsworth-Emmons reaction;
DOI:10.1002/chem.200501128