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HRID 732343Erstellt: 24. Oktober 2026

2,2,6,6-Tetramethylpiperidine → HCID 68814650, Verbindung

https://huagongshe.com/de/reaction/732343

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2,2,6,6-TetramethylpiperidineHCID 13035—
Edukttert-butyl 1H-pyrrole-1-carboxylateHCID 643494—
EduktHCID 86614992HCID 86614992—
EduktButyllithiumHCID 178418339—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktHCID 68814650HCID 6881465010%

Reaktionsbedingungen

Temperatur-10 °C

Reaktionsschritte

Add n-butyllithium (3.30 mL, 8.25 mmol, 2.5 M in hexanes) to a solution of 2,2,6,6-tetramethylpiperidine (1.40 mL, 8.18 mmol) in tetrahydrofuran (THF) (30 mL) at −78° C. over 2 min. Stir 5 min, then warm to −10° C. and stir 5 min, then cool to −78° C. Add N-tert-butoxycarbonylpyrrole (1.37 mL, 8.25 mmol) in THF (1.6 mL) over 3 min. Stir 30 min and add 2-(S)-[bis-(2-methylbenzyl)-amino]-3-(3,5-difluorophenyl)-propionaldehyde (2.96 g, 7.44 mmol) in THF (15 mL) over 5 min. Stir 60 min at −78° C., warm to 0° C. and stir 60 min. Cool −78° C. and quench with saturated aqueous ammonium chloride solution. Extract with ethyl acetate, dry (magnesium sulfate), concentrate and purify (silica gel chromatography, eluting with hexanes and dichloromethane) to give the title compound as a foam (0.416 g, 10%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07585885B2
Quelldatensatzuspto-grants-2009_09
ORD IDord-8e478015b76044cc98413c62c33f9d85
Quellennotizuspto-grants-2009_09