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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1402713Erstellt: 26. Oktober 2026

Triphenylphosphine → (R)-4-((R)-1-(7-(pyridin-2-yl)quinolin-5-yloxy)ethyl)pyrrolidin-2-one

https://huagongshe.com/reaction/1402713

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriphenylphosphineHCID 11776—
EduktDibenzyl azodicarboxylateHCID 5387121—
Edukt(R)-4-((S)-1-hydroxyethyl)-1-((S)-1-(4-methoxyphenyl)ethyl)pyrrolidin-2-oneHCID 58071870—
Edukt7-(Pyridin-2-yl)quinolin-5-olHCID 136413252—
LösungsmittelDichloromethaneHCID 6344—
Produkt(R)-4-((R)-1-(7-(pyridin-2-yl)quinolin-5-yloxy)ethyl)pyrrolidin-2-oneHCID 71238245—

Reaktionsschritte

20 mg of 7-(Pyridin-2-yl)quinolin-5-ol, 30 mg of ((R)-4-((S)-1-hydroxyethyl)-1-((S)-1-(4-methoxyphenyl)ethyl)pyrrolidin-2-one and 50 mg of triphenylphosphin was dissolved in 2 mL of DCM. 45 mg of DBAD was added and the mixture stirred for 14 h at room temperature. The mixture was diluted with DCM and extracted with 1N NaOH and water. The organic phase was concentrated in vacuo and dissolved in 0.5 mL of TFA and heated 30 min at 90° C. in the microwave. The mixture was purified with HPLC (XbridgeC18, MeOH/water, TFA) to yield after lyophilisation 21 mg of Example 6 as solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08912173B2
Quelldatensatzuspto-grants-2014_12
ORD IDord-fe28971e8b7e4d9abc1a3b589818a4cb
Quellennotizuspto-grants-2014_12