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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1890734Generated: October 30, 2026

Toluene → 3-(Isoquinolin-3-yl)-4-methylaniline

https://huagongshe.com/reaction/1890734

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantSodium CarbonateHCID 10340—
Reactant3-ChloroisoquinolineHCID 640968—
Reactant4-Methyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)anilineHCID 16086089—
CatalystHCID 178418397HCID 178418397—
SolventEthanolHCID 702—
Product3-(Isoquinolin-3-yl)-4-methylanilineHCID 58317885—

Reaction Conditions

Temperature90 °C

Reaction Steps

To a round-bottom flask containing 5-amino-2-methyl-phenylboronic acid pinacol ester (233 mg, 1 mmol), 3-chloro-isoquinoline (245 mg, 1.5 mmol), Pd(PPh3)4 (128 mg, 0.1 mmol) is added toluene (4 ml), EtOH (1 ml) and aqueous 2M Na2CO3 solution (2 ml). The flask is purged with argon and sealed. The mixture is stirred at 90° C. for 18 hours, cooled to room temperature and extracted using water and ethyl acetate. The organic layer is separated, washed with brine, dried over MgSO4 and concentrated. The residue is subjected to silica gel flash chromatography, eluted with ethyl acetate in hexanes from 30% to 50% to afford 3-(isoquinolin-3-yl)-4-methylaniline as a brown oil. LC-MS m/z: 235.1 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08507491B2
Source datasetuspto-grants-2013_08
ORD IDord-77bd56dcd6fe46cf854d539285089f4a
Source noteuspto-grants-2013_08