1-Iodopropane → Methyl 2-(4-methyl-2-(piperidin-1-yl)-6-p-tolylpyrimidin-5-yl)pentanoate

Temperatur

-15 °C

A solution of methyl 2-(4-methyl-2-(piperidin-1-yl)-6-p-tolylpyrimidin-5-yl)acetate (160 mg; 0.471 mmol) in dry DMF (2.5 mL) was cooled to −15° C. LHMDS (0.519 mL; 0.519 mmol; 1M in THF) was added dropwise and the mixture was stirred at −15° C. for 15 min followed by the dropwise addition of iodopropane (0.069 mL; 0.707 mmol), after stirring for 2 h at −15° C. the mixture was allowed to warm up to room temperature. After 1 h the reaction was quenched by adding a saturated solution of ammonium chloride. The mixture was extracted twice with ethyl acetate and the combined organic layers were washed with brine, dried over magnesium sulphate and concentrated under reduced pressure. The crude material was purified by flash chromatography on silica gel using a linear gradient of ethylacetate (2-10%) in heptane to give 63 mg (34%) of the title compound as a yellow oil. ESI/APCI(+): 382 (M+H).

1. stirringafter stirring for 2 h at −15° C. the mixture
2. temperatureto warm up to room temperature
3. customAfter 1 h the reaction was quenched
4. additionby adding a saturated solution of ammonium chloride
5. extractionThe mixture was extracted twice with ethyl acetate
6. washthe combined organic layers were washed with brine
7. dry with materialdried over magnesium sulphate
8. concentrationconcentrated under reduced pressure
9. customThe crude material was purified by flash chromatography on silica gel using a linear gradient of ethylacetate (2-10%) in heptane

ORD-Eintrag

ord-72403608696844c5ab1969667cb32d8b

Quelldatensatz

uspto-grants-2014_12

DOI

10.6084/m9.figshare.5104873.v1

Patentnummer

US08906906B2