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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1033521Generated: October 26, 2026

O-Methyltyramine → 5,6,7,8-Tetrahydro-5-[[2-(4-methoxyphenyl)ethyl]amino]-1-methyl-2(1H)-quinolinone

https://huagongshe.com/reaction/1033521

Reaction equation

Participants

RoleNameHCIDCharge
ReactantO-MethyltyramineHCID 4657—
Reactantp-Toluenesulfonic acidHCID 6101—
Reactant1-Methyl-7,8-dihydroquinoline-2,5(1H,6H)-dioneHCID 10442242—
SolventTolueneHCID 1140—
Product5,6,7,8-Tetrahydro-5-[[2-(4-methoxyphenyl)ethyl]amino]-1-methyl-2(1H)-quinolinoneHCID 1008688481%

Reaction Steps

A mixture of 2-(4-methoxyphenyl)ethylamine (5.6 g), 5,6,7,8-tetrahydro-1-methyl-5-oxo-2(1H)-quinolinone (5.5 g), and a catalytic amount of para-toluenesulfonic acid was heated in refluxing toluene (90 ml), with azeotropic removal of water, for 39 hrs. The solution was cooled and concentrated in vacuo. Sodium borohydride (1.1 g) was added to a solution of the residue in ethyl alcohol (90 ml), and the mixture was stirred at room temperature for 2 hrs. The mixture was concentrated in vacuo, the residue was quenched with water, and the mixture was extracted with dichloromethane. The combined organic layers were washed with brine, dried over anhydrous magnesium sulfate, filtered, and the filtrate was concentrated. The residue was washed with diethyl ether to afford 7.8 g (81%) of product. Recrystallization from ethyl acetate/hexanes provided the analytical sample, mp 97°-99° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05310914
Source datasetuspto-grants-1994_05
ORD IDord-93adbae73078457caa96daf3e022cf96
Source noteuspto-grants-1994_05