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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1173978Generated: October 25, 2026

3-[6-(1,3-Dioxo-1,3-dihydro-isoindol-2-ylmethyl)-quinolin-2-yl]-acrylonitrile → 3-[6-(1,3-Dioxo-1,3-dihydro-isoindol-2-ylmethyl)-quinolin-2-yl]-propionitrile

https://huagongshe.com/reaction/1173978

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-[6-(1,3-Dioxo-1,3-dihydro-isoindol-2-ylmethyl)-quinolin-2-yl]-acrylonitrileHCID 66941508—
CatalystHCID 178502593HCID 178502593—
SolventEthanolHCID 702—
SolventChloroformHCID 6212—
Product3-[6-(1,3-Dioxo-1,3-dihydro-isoindol-2-ylmethyl)-quinolin-2-yl]-propionitrileHCID 2108440217.6%

Reaction Steps

The compound (574.4 mg) obtained in Example 119-6 was dissolved in ethanol (20 ml) and chloroform (10 ml). Then, the solution was added with 20% palladium hydroxide-carbon (172.3 mg) and then stirred at room temperature for 16 hours under a hydrogen atmosphere. After the reaction, the solution was filtrated through Celite and the solvent was then distilled off under reduced pressure. The residue was purified through silica gel column chromatography (hexane/ethyl acetate), thereby obtaining the subject compound (101.9 mg) as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07833991B2
Source datasetuspto-grants-2010_11
ORD IDord-7c66fcd8d21b4572ac0d1ea545416a8b
Source noteuspto-grants-2010_11