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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1468811Erstellt: 25. Oktober 2026

Sodium Iodide → Morpholine, 4-(2-(2-nitro-1H-imidazol-1-yl)ethyl)-

https://huagongshe.com/reaction/1468811

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium IodideHCID 5238—
Edukt2-NitroimidazoleHCID 10701—
EduktMorpholine, 4-(2-chloroethyl)-, hydrochloride (1:1)HCID 77210—
EduktSodium MethoxideHCID 10942334—
LösungsmittelDimethylformamideHCID 6228—
ProduktMorpholine, 4-(2-(2-nitro-1H-imidazol-1-yl)ethyl)-HCID 10057358%

Reaktionsbedingungen

Temperatur100 °C

Reaktionsschritte

2-Nitroimidazole (0.55 g, 4.86 mmol), 4-(2-chloroethyl)morpholine hydrochloride (0.90 g, 4.86 mmol), sodium iodide (0.18 g, 1.21 mmol) and sodium methoxide (0.59 g, 10.0 mmol) are dissolved in DMF (25 mL). The mixture is heated at 100° C. under a nitrogen atmosphere for 14 h. The reaction mixture is cooled and solvent removed in vacuo. The residue is partitioned between ethyl acetate (30 mL) and sat. NaHCO3 (aq.) (30 mL). The aqueous layer is extracted with ethyl acetate (4×30 mL). The organic layers are combined, dried (MgSO4) and solvent removed in vacuo. The solid residue is purified by column chromatography, eluting with 3% methanol in dichloromethane to give a yellow oil (638 mg, 58%). 1H-NMR (400 MHz, d6-DMSO) =2.39-2.45 (m, 4H), 2.66 (t, 2H, J=6 Hz), 3.52 (t, 4H, J=4.8 Hz), 4.52-4.54 (t, 2H, J=6 Hz), 7.19 (s, 1H, Har), 7.68 (s, 1H, Har).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09006237B2
Quelldatensatzuspto-grants-2015_04
ORD IDord-093dbf4da7b94775bfa460898e1b990f
Quellennotizuspto-grants-2015_04