Methyl 1-(pyridin-4-yl)piperidine-4-carboxylate → (1-(Pyridin-4-YL)piperidin-4-YL)methanol

Temperatur

0 °C

A solution of methyl N-(4-pyridyl)isonipecotate (600 mg, 2.72 mmol) in tetrahydrofuran was added to solution of lithium aluminum hydride (100 mg) in tetrahydrofuran (14 mL) cooled to 0° C. Upon consumption of the starting material (0.5-2 h), the mixture was treated with water (0.10 mL), 15% aqueous sodium hydroxide (0.10 mL), and water (0.30 mL). After 0.25 h, the mixture was sonicated for 0.25 h, then poured into a mixture of ethyl acetate, water, sodium tartrate, and potassium tartrate. The aqueous layer was extracted twice with ethyl acetate and the combined extracts were dried (magnesium sulfate), filtered, and concentrated in vacuo to yield 357 mg (68%) of the title compound, which was used without further purification.

1. customUpon consumption of the starting material (0.5-2 h)
2. additionthe mixture was treated with water (0.10 mL), 15% aqueous sodium hydroxide (0.10 mL), and water (0.30 mL)
3. customthe mixture was sonicated for 0.25 h
4. additionpoured into a mixture of ethyl acetate, water, sodium tartrate, and potassium tartrate
5. extractionThe aqueous layer was extracted twice with ethyl acetate
6. dry with materialthe combined extracts were dried (magnesium sulfate)
7. filtrationfiltered
8. concentrationconcentrated in vacuo

ORD-Eintrag

ord-105cc03e530e4ace8dfeec4c9202fb19

Quelldatensatz

uspto-grants-2003_08

DOI

10.6084/m9.figshare.5104873.v1

Patentnummer

US06605626B2