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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2044909Erstellt: 25. Oktober 2026

Dimethyl Ether → 2-((S)-1-(8-chloro-2-(2-chloro-5-fluoropyridin-3-yl)quinolin-3-yl)-ethyl)isoindoline-1,3-dione

https://huagongshe.com/reaction/2044909

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDimethyl EtherHCID 8254—
EduktCesium fluorideHCID 25953—
Edukt2-Chloro-5-fluoropyridine-3-boronic acidHCID 24901774—
Edukt(S)-2-(1-(2,8-dichloroquinolin-3-yl)ethyl)isoindoline-1,3-dioneHCID 57707774—
KatalysatorCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
KatalysatorHCID 178418397HCID 178418397—
LösungsmittelEthylene GlycolHCID 174—
Produkt2-((S)-1-(8-chloro-2-(2-chloro-5-fluoropyridin-3-yl)quinolin-3-yl)-ethyl)isoindoline-1,3-dioneHCID 86630634—

Reaktionsschritte

A mixture of (S)-2-(1-(2,8-dichloroquinolin-3-yl)ethyl)isoindoline-1,3-dione (120.0 mg, 323 μmol), 2-chloro-5-fluoropyridin-3-ylboronic acid (57 mg, 323 mmol), tetrakis(triphenylphosphine)palladium (37 mg, 32 μmol), cesium fluoride (147 mg, 970 μmol) and copper(I) iodide (12 mg, 65 μmol) in 1,2-ethanediol, dimethyl ether (3.0 mL, 323 μmol) was subjected to microwave at 100° C. for 1 h, cooled to room temperature. Filtration of the resultant mixture and rinsed with EtOAc, the filtrates were collected and concentrated. Purification of the residue by flash chromatography over silica gel, gradient elution, 0-100% EtOAc in hexane, gave 2-((S)-1-(8-chloro-2-(2-chloro-5-fluoropyridin-3-yl)quinolin-3-yl)-ethyl)isoindoline-1,3-dione, Mass Spectrum (ESI) m/e=466.0 (M+1).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08586739B2
Quelldatensatzuspto-grants-2013_11
ORD IDord-fc04a52094f84b5289b9a9e299e09e2b
Quellennotizuspto-grants-2013_11