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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 8153Erstellt: 24. Oktober 2026

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

https://huagongshe.com/de/reaction/8153

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).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07087629B2
Quelldatensatzuspto-grants-2006_08
ORD IDord-d9bb5586c23743ebb695b08c565f0db1
Quellennotizuspto-grants-2006_08