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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 425894Erstellt: 24. Oktober 2026

N-bromobutanimide → 3-(Benzyloxy)-5-bromopyridin-2-amine

https://huagongshe.com/de/reaction/425894

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktN-bromobutanimideHCID 67184—
Edukt2-Amino-3-benzyloxypyridineHCID 90334—
LösungsmittelAcetonitrileHCID 6342—
LösungsmittelEthyl AcetateHCID 8857—
Produkt3-(Benzyloxy)-5-bromopyridin-2-amineHCID 2062655453%

Reaktionsschritte

To a stirred solution of 2-amino-3-benzyloxypyridine (42.0 g, 0.21 mol) in CH3CN (600 mL) at 0° C. was added N-bromosuccinimide (37.1 g, 0.21 mol) over 30 minutes. The mixture was stirred for 0.5 hr, after which the reaction was then diluted with EtOAc (900 mL) and partitioned with H2O (900 mL). The organic layer was, washed with brine and dried (Na2SO4), filtered and concentrated to dryness under vacuum to yield 3-benzyloxy-5-bromo-pyridin-2-ylamine (31.0 g, 0.11 mol, 53%). 1H NMR (CDCl3, 300 MHz) δ 4.63-4.78 (brs, 2H), 5.04 (s, 2H), 7.07 (d, 1H, J, 1.8 Hz), 7.33-7.42 (m, 5H), 7.73 (d, 1H, J, 1.8 Hz).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08106197B2
Quelldatensatzuspto-grants-2012_01
ORD IDord-c82cf1b949b640d692dc8323f8b26d6f
Quellennotizuspto-grants-2012_01