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HRID 472027Erstellt: 25. Oktober 2026

Water → 5-(2,6-Diethyl-Phenyl)-1-(4,6-Dimethyl-Pyrimidin-2-YL)-1H-Pyrrolo[2,3-c]Pyridine

https://huagongshe.com/reaction/472027

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
Edukt2-Chloro-4,6-dimethylpyrimidineHCID 20550—
EduktSodium hydrideHCID 24758—
Edukt5-(2,6-diethyl-phenyl)-1H-pyrrolo[2,3-c]pyridineHCID 11673246—
LösungsmittelDimethylformamideHCID 6228—
LösungsmittelEthyl AcetateHCID 8857—
Produkt5-(2,6-Diethyl-Phenyl)-1-(4,6-Dimethyl-Pyrimidin-2-YL)-1H-Pyrrolo[2,3-c]PyridineHCID 58269946—

Reaktionsschritte

To a solution of 5-(2,6-diethyl-phenyl)-1H-pyrrolo[2,3-c]pyridine (10 mg, 0.04 mmol) in DMF (0.5 mL) is added NaH (95%, 3 mg). The reaction mixture is stirred at room temperature for 30 minutes, and then 2-chloro-4,6-dimethyl-pyrimidine (17 mg, 0.12 mmol)) is added. The mixture is heated at 60° C. overnight and cooled. Water (1 mL) and EtOAc (2 mL) are added to the mixture. The organic layer is separated, washed with water once and concentrated under reduced pressure. The residue is purified by PTLC (Hexane/EtOAc 4:1) to give the titled compound. 1H NMR: (CDCl3) 10.21 (s, 1H), 8.48 (d, 1H), 7.47 (s, 1H), 7.28 (t, 1H), 7.15 (d, 2H), 6.87 (s, 1H), 6.68 (d, 1H), 2.55 (s, 6H), 2.36 (m, 4H), 1.03 (t, 6H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08633193B2
Quelldatensatzuspto-grants-2014_01
ORD IDord-3cb85de494f241969c696bd7123f3495
Quellennotizuspto-grants-2014_01