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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2044878Generated: October 27, 2026

Ethyl Acetate → 2-(1-(5-Chloro-2-(pyridin-2-yl)quinolin-3-yl)ethyl)isoindoline-1,3-dione

https://huagongshe.com/reaction/2044878

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
Reactant2-(Tributylstannyl)pyridineHCID 607784—
Reactant2-(1-(2,5-Dichloroquinolin-3-yl)ethyl)isoindoline-1,3-dioneHCID 57707873—
CatalystHCID 178418397HCID 178418397—
SolventTolueneHCID 1140—
Product2-(1-(5-Chloro-2-(pyridin-2-yl)quinolin-3-yl)ethyl)isoindoline-1,3-dioneHCID 57707828—

Reaction Conditions

Temperature110 °C

Reaction Steps

Transferred 2-(1-(2,5-dichloroquinolin-3-yl)ethyl)isoindoline-1,3-dione (197 mg, 531 μmol) from 100 mL flask to 10 mL flask by dissolving/slurrying in toluene and concentrating. Added Pd(Ph3P)4 (61 mg, 53 μmol) and 2-tri-n-butylstannylpyridine (955 μl, 2653 μmol). Bubbled argon through mixture for 30 sec. Equipped with condensor and nitrogen inlet. Heated at 110° C. for ˜16 h. The reaction mixture was concentrated and chromatographed on 12 g silica gel column with 0-60% EtOAc. The desired fractions were combined and concentrated to yield an oil. NMR indicates residual EtOAc. LC. 1H NMR (400 MHz, DICHLOROMETHANE-d2) δ ppm 1.98 (d, J=7.04 Hz, 3 H) 6.38 (q, J=7.04 Hz, 1 H) 7.24-7.37 (m, 1 H) 7.62-7.76 (m, 8 H) 8.01 (dd, J=8.61, 1.96 Hz, 1 H) 8.56-8.66 (m, 1 H) 9.02 (s, 1 H).−MS (+esi, M+H+=414.1)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08586739B2
Source datasetuspto-grants-2013_11
ORD IDord-1af307bdf8714fe39531c52068828a8f
Source noteuspto-grants-2013_11