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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1582337Erstellt: 26. Oktober 2026

Pyridine → 5-Benzyloxycarbonylamino-2-(2-methyl-imidazol-1-yl)fluorobenzene

https://huagongshe.com/reaction/1582337

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPyridineHCID 1049—
EduktBenzyl chloroformateHCID 10387—
EduktSodium BicarbonateHCID 516892—
Edukt3-fluoro-4-(2-methyl-1H-imidazol-1-yl)anilineHCID 21876620—
LösungsmittelDichloromethaneHCID 6344—
Produkt5-Benzyloxycarbonylamino-2-(2-methyl-imidazol-1-yl)fluorobenzeneHCID 2187665193,5%

Reaktionsschritte

5-Amino-2-(2-methylimidazol-1-yl)fluorobenzene (34.25 g, 0.179 M) was dissolved in dry dichloromethane (600 ml) under nitrogen, and cooled to −5°. Pyridine (17.7 g, 0.224 M) was added, followed by benzyl chloroformate (33.7 g, 0.197 M) over 20 minutes. The mixture was stirred and the temperature allowed to rise to ambient over 16 hours. Aqueous sodium bicarbonate (5%, 250 ml) was added, the organic layer separated, the aqueous layer re-extracted with dichloromethane (2×300 ml), and combined extracts dried (magnesium sulfate). After filtration and evaporation, the residue was recrystallised from toluene (400 ml) to give title product (54.5 g). NMR (DMSO-d6) δ: 2.13 (s, 3H); 5.18 (s, 2H); 6.89 (s, 1H); 7.17 (s, 1H); 7.41 (overlapping m, 7H); 7.73 (dd, 1H); 10.21 (br, 1H). MS (ESP): 326 (MH+) for C18H16FN3O2

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06734200B1
Quelldatensatzuspto-grants-2004_05
ORD IDord-71348f1e773d4121a09a5c5e9061104a
Quellennotizuspto-grants-2004_05