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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1496866Generated: October 26, 2026

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

https://huagongshe.com/reaction/1496866

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantDibenzyl azodicarboxylateHCID 5387121—
Reactant(R)-4-((S)-1-hydroxyethyl)-1-((S)-1-(4-methoxyphenyl)ethyl)pyrrolidin-2-oneHCID 58071870—
Reactant7-(Pyridin-2-yl)quinolin-5-olHCID 136413252—
SolventDichloromethaneHCID 6344—
Product(R)-4-((R)-1-(7-(pyridin-2-yl)quinolin-5-yloxy)ethyl)pyrrolidin-2-oneHCID 71238245—

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09199937B2
Source datasetuspto-grants-2015_12
ORD IDord-206d6d8b98234a27bbd26e949ceffeca
Source noteuspto-grants-2015_12