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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2284570Erstellt: 25. Oktober 2026

Sodium Carbonate → 6-(2-Chloropyridin-3-yl)imidazo[1,2-a]pyridine

https://huagongshe.com/reaction/2284570

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium CarbonateHCID 10340—
Edukt6-Iodoimidazo(1,2-a)pyridineHCID 2764327—
Edukt2-Chloropyridine-3-boronic acid pinacol esterHCID 12067060—
Edukt6-(2-Chloropyridin-3-yl)benzo[d]thiazoleHCID 86715476—
KatalysatorHCID 178418397HCID 178418397—
Lösungsmittel1,4-DioxaneHCID 31275—
Produkt6-(2-Chloropyridin-3-yl)imidazo[1,2-a]pyridineHCID 8671547855%

Reaktionsschritte

6-(2-Chloropyridin-3-yl)imidazo[1,2-a]pyridine was synthesized in the similar to 6-(2-chloropyridin-3-yl)benzo[d]thiazole from 6-iodo-imidazo[1,2-a]pyridine (1.0 g, 4.1 mmol), 2-chloro-3-pyridine boronic acid pinacol ester (1.2 g, 5.0 mmol), Pd(PPh3)4 (250 mg, 0.22 mmol) and 2M aq.Na2CO3 (7 mL, 12 mmol) in 1,4-dioxane (50 mL). Workup of the reaction mixture was carried out by sequential steps of concentrating the reaction mixture, extraction with CH2Cl2, drying over MgSO4/Celite®, filtration and concentration. The crude residue was stirred in 50% EtOAc/hexanes (40 mL). The resulting white precipitate was filtered and dried to provide 6-(2-chloropyridin-3-yl)imidazo[1,2-a]pyridine (0.52 g, 55%). 1H NMR (DMSO-d6): δ 8.73 (dd, 1H, J=0.8 and 1.8 Hz), 8.47 (dd, 1H, J=2.0 and 4.7 Hz), 8.00 (dd, 1H, J=2.0 and 7.6 Hz), 7.98 (s, 1H), 7.64 (d, 1H, J=8.8 Hz), 7.63 (s, 1H), 7.56 (dd, 1H, J=4.7 and 7.6 Hz), 7.33 (dd, 1H, J=1.8 and 8.8 Hz), Hz).LCMS: rt 3.16 min (A), purity 99%, MS (m/e) 230 (MH+).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09145433B2
Quelldatensatzuspto-grants-2015_09
ORD IDord-8818e424071048ed848a50b056d18235
Quellennotizuspto-grants-2015_09