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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 271121Erstellt: 26. Oktober 2026

4-Fluoro-3-(tributylstannyl)pyridine → 2-Amino-5-(2,6-diethyl-pyridin-4-yl)-5-[4-fluoro-3-(4-fluoropyridin-3-yl)-phenyl]-3-methyl-3,5-dihydro-imidazol-4-one

https://huagongshe.com/reaction/271121

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt4-Fluoro-3-(tributylstannyl)pyridineHCID 16427151—
Edukt2-Amino-5-(3-bromo-4-fluorophenyl)-5-(2,6-diethyl-pyridin-4-yl)-3-methyl-3,5-dihydro-imidazol-4-oneHCID 59834558—
KatalysatorHCID 178479804HCID 178479804—
LösungsmittelDimethylformamideHCID 6228—
Produkt2-Amino-5-(2,6-diethyl-pyridin-4-yl)-5-[4-fluoro-3-(4-fluoropyridin-3-yl)-phenyl]-3-methyl-3,5-dihydro-imidazol-4-oneHCID 5983457710%

Reaktionsbedingungen

Temperatur150 °C

Reaktionsschritte

A mixture of 2-amino-5-(3-bromo-4-fluorophenyl)-5-(2,6-diethyl-pyridin-4-yl)-3-methyl-3,5-dihydro-imidazol-4-one (0.170 g, 0.405), 4-fluoropyridin-3-yl(tributly)tin (0.235 g, 0.608 mmol) and bis(triphenylphosphino)palladium(II) chloride (0.023 g, 0.032 mmol) in DMF (5 mL) was degassed and heated at 150° C. for 1 h. The mixture was cooled to room temperature and diluted with ethyl acetate (50 mL) and 2% aqueous lithium chloride (20 mL). The organic layer was separated, washed with 2% aqueous lithium chloride, dried over sodium sulfate, filtered, and concentrated. Purification of the resultant residue by flash chromatography (silica, 95:5:0.25 methylene chloride/methanol/concentrated ammonium hydroxide) afforded the title product (0.017 g, 10%) as a white solid, mp 92-100° C.; 1H NMR (300 MHz, CD3OD) δ 8.55-8.45 (m, 2H), 7.56-7.19 (m, 4H), 7.09 (s, 2H), 3.10 (s, 3H), 2.68 (q, J=7.5 Hz, 4H), 1.15 (t, J=7.5 Hz, 6H); ESI MS m/z 436 [C24H23F2N5O+OH]+.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07452885B2
Quelldatensatzuspto-grants-2008_11
ORD IDord-6486f40020e549b890f08825eb036461
Quellennotizuspto-grants-2008_11