2(1H)-Pyrimidinone, tetrahydro-1,3-dimethyl- → Ethyl 2-(4-methanesulfonylphenyl)-3-(tetrahydropyran-4-yl)propionate

Temperatur

20 °C

LDA (38.9 mL of a 1.8M solution in n-C7H16-THF-PhEt, 70.0 mmol) was added to a solution of DMPU (59.3 mL, 490.3 mmol) in anhydrous THF (150 mL) at −78° C. The mixture was stirred for 30 min, before being treated dropwise with a solution of ethyl (4-methanesulfonylphenyl)acetate (Preparation 15, 16.97 g, 70.0 mmol) in anhydrous THF (50 mL). Stirring was continued at −78° C. for 45 min, then a solution of 4-iodomethyltetrahydropyran (19.00 g, 84.0 mmol) in anhydrous THF (40 mL) was added. The mixture was allowed to warm to 20° C. over 16 h, before being quenched with 1M HCl (70 mL). The THF was removed under reduced pressure, then more H2O (40 mL) was added and the remainder extracted with EtOAc (2×250 mL). The EtOAc extracts were dried (MgSO4). Filtration, solvent evaporation, and flash chromatography (IH-EtOAc, 9:1 to 1:1) furnished ethyl 2-(4-methanesulfonylphenyl)-3-(tetrahydropyran-4-yl)propionate: m/z (ES+)=698.3 [2M+NH4]+. A solution of this compound (20.27 g, 59.6 mmol) in MeOH (100 mL) and 2M NaOH (62.5 mL, 125.0 mmol) was heated under reflux for 1 h. The solvents were removed under reduced pressure, then the remaining solid was triturated with Et2O (5×100 mL), before being dissolved in H2O (100 mL). The aqueous solution was washed with EtOAc (50 mL), acidified with 2M HCl to pH 1, and extracted with EtOAc (2×1 L). After drying (MgSO4), filtration and solvent evaporation gave the title compound: m/z (ES+)=642.3 [2M+NH4]+.

1. stirringStirring
2. waitwas continued at −78° C. for 45 min
3. custombefore being quenched with 1M HCl (70 mL)
4. customThe THF was removed under reduced pressure
5. additionmore H2O (40 mL) was added
6. extractionthe remainder extracted with EtOAc (2×250 mL)
7. dry with materialThe EtOAc extracts were dried (MgSO4)
8. filtrationFiltration, solvent evaporation, and flash chromatography (IH-EtOAc, 9:1 to 1:1)

ORD-Eintrag

ord-d683022ad48c428c9541ef1c4705b469

Quelldatensatz

uspto-grants-2007_05

DOI

10.6084/m9.figshare.5104873.v1

Patentnummer

US07214681B2