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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1821916Erstellt: 26. Oktober 2026

[7-(dibenzylamino)-1H-pyrrolo[2,3-c]pyridin-2-yl]methanol → 7-(dibenzylamino)-1H-pyrrolo[2,3-c]pyridine-2-carboxaldehyde

https://huagongshe.com/reaction/1821916

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt[7-(dibenzylamino)-1H-pyrrolo[2,3-c]pyridin-2-yl]methanolHCID 68981956—
KatalysatorHCID 178418406HCID 178418406—
LösungsmittelMethyl, chloro-HCID 5378701—
Produkt7-(dibenzylamino)-1H-pyrrolo[2,3-c]pyridine-2-carboxaldehydeHCID 5789350360%

Reaktionsschritte

[7-(Dibenzylamino)-1H-pyrrolo[2,3-c]pyridin-2-yl]methanol (3.0 g, 8.74 mmol) was dissolved in methylene chlorine (175 mL). Manganese dioxide (8.0 g, 92 mmol) was added and the reaction mixture was stirred at room temperature for 20 h. The slurry was filtered through diatomaceous earth to remove the catalyst, and the filtrate was concentrated to a dark oil. Purification by Biotage chromatography (10-30% ethyl acetate in hexanes) provided 7-(dibenzylamino)-1H-pyrrolo[2,3-c]pyridine-2-carboxaldehyde (1.78 g, 60%) as a yellow oil: 1H NMR (300 MHz, CDCl3) δ4.89 (4H, s), 7.06-7.12 (2H, m), 7.27-7.38 (10H, m), 7.93 (1H, d, J=5.7 Hz), 8.74 (1H, br s), 9.77 (1H, s).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07608627B2
Quelldatensatzuspto-grants-2009_10
ORD IDord-c1c4f3fb22ea4648afcab6b4086067e5
Quellennotizuspto-grants-2009_10