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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 588401Erstellt: 24. Oktober 2026

6-Azaindole → tert-Butyl 4-{1H-pyrrolo[2,3-c]pyridin-3-yl}-1,2,3,6-tetrahydropyridine-1-carboxylate

https://huagongshe.com/de/reaction/588401

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt6-AzaindoleHCID 9219—
EduktPotassium HydroxideHCID 14797—
Edukttert-Butyl 4-oxopiperidine-1-carboxylateHCID 735900—
LösungsmittelMethanolHCID 887—
Produkttert-Butyl 4-{1H-pyrrolo[2,3-c]pyridin-3-yl}-1,2,3,6-tetrahydropyridine-1-carboxylateHCID 5955936992%

Reaktionsschritte

A suspension of 1H-pyrrolo[2,3-c]pyridine (0.95 g, 8.05 mmol), tert-butyl 4-oxo-piperidine-1-carboxylate (1.70 g, 8.54 mmol) and KOH (0.95 g, 17.0 mmol) in MeOH (10 mL) was heated at reflux overnight. The mixture was added to ice-water (50 mL) and then MeOH (50 mL) was added. The resulting solution was concentrated to circa 50 mL and then extracted three times with DCM/MeOH (9:1, 50 mL). The organic layers were combined and concentrated and the residue was purified by flash chromatography (9:1 DCM/MeOH) to yield the title compound as a light yellow solid (2.21 g, 92%). MS (ESI+) m/z=300 (M+H)+.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09227967B2
Quelldatensatzuspto-grants-2016_01
ORD IDord-ef0c13e8c0354ee09168905c946e3d4d
Quellennotizuspto-grants-2016_01