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HRID 456716Erstellt: 24. Oktober 2026

N-Iodosuccinimide → 8-(Benzyloxy)-2-(4-fluorophenyl)-3-iodoimidazo[1,2-a]pyridine

https://huagongshe.com/de/reaction/456716

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktN-IodosuccinimideHCID 120273—
Edukt8-(Benzyloxy)-2-(4-fluorophenyl)imidazo[1,2-a]pyridineHCID 18436714—
LösungsmittelDimethylformamideHCID 6228—
Produkt8-(Benzyloxy)-2-(4-fluorophenyl)-3-iodoimidazo[1,2-a]pyridineHCID 18436713—

Reaktionsschritte

To a 0° C. solution of 8-(benzyloxy)-2-(4-fluorophenyl)imidazo[1,2-a]pyridine (0.25 g, 0.79 mmol) in N,N-dimethylformamide (8.0 mL) was added dropwise a solution of N-iodosuccinimide (0.17 g, 0.79 mmol) in N,N-dimethylformamide (4 mL). The reaction was stirred for 2.5 hours and concentrated to a volume of 2 mL The mixture was diluted with ethyl acetate, washed twice with 1M aqueous sodium hydroxide, and concentrated. The residue was purified by silica gel chromatography, eluting with 5% acetone in dichloromethane to yield 0.23 (67%) of 8-(benzyloxy)-2-(4-fluorophenyl)-3-iodoimidazo[1,2-a]pyridine. 1H NMR (CDCl3): δ 8.10 (dd, 2H), 7.90 (d, 1H), 7.53 (d, 2H), 7.40 (m, 3H), 7.19 (t, 2H), 6.81 (t, 1H), 6.61 (d, 1H), 5.46 (s, 2H); MS m/z 445 (M+1).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07186714B2
Quelldatensatzuspto-grants-2007_03
ORD IDord-01600c0d61b74b45b7e269959c5a72b7
Quellennotizuspto-grants-2007_03