Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1403764Erstellt: 25. Oktober 2026

Stannane, tributyl[5-(1,3-dioxolan-2-yl)-2-furanyl]- → (4-Phenoxyphenyl)-(7-(5-(1,3-dioxolan-2-yl)furan-2-yl)-quinolin-4-yl)amine

https://huagongshe.com/reaction/1403764

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktStannane, tributyl[5-(1,3-dioxolan-2-yl)-2-furanyl]-HCID 10960952—
Edukt(4-Phenoxyphenyl)-(7-iodoquinolin-4-yl)amineHCID 21952018—
KatalysatorTetrakis(triphenylphosphine)palladiumHCID 11979704—
LösungsmittelDimethylacetamideHCID 31374—
Produkt(4-Phenoxyphenyl)-(7-(5-(1,3-dioxolan-2-yl)furan-2-yl)-quinolin-4-yl)amineHCID 2195223768,1%

Reaktionsschritte

(4-Phenoxyphenyl)-(7-iodo-quinolin-4-yl)amine (2 g) was treated with 2-(tributylstannyl)-5-(1,3-dioxolan-2-yl)-furan (2.16 g) and tetrakis (triphenylphosphine) palladium (0) (0.26 g) in dimethylacetamide (20 ml) in accordance with Procedure B. Purification via column chromatography, eluting with ethyl acetate, followed by trituration with diethylether afforded a yellow solid (1.4 g); δ H [2H6] DMSO 9.10 (1H, s), 8.45 (2H, m), 8.13 (1H, s), 7.96 (1H, d), 7.41 (4H, m), 7.22 (1H, d), 7.20-7.03 (5H, m), 6.83 (1H, d), 6.75 (1H, d), 6.02 (1H, s), 4.13 (2H, m), 4.01 (2H, m); m/z 451 (M+1)+.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08912205B2
Quelldatensatzuspto-grants-2014_12
ORD IDord-eb0a77f32f0d4a85bdd6089bf3bc7618
Quellennotizuspto-grants-2014_12