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
Participants
| Role | Name | HCID | Charge |
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| Reactant | O-Methyltyramine | HCID 4657 | — |
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | 1-Methyl-7,8-dihydroquinoline-2,5(1H,6H)-dione | HCID 10442242 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 5,6,7,8-Tetrahydro-5-[[2-(4-methoxyphenyl)ethyl]amino]-1-methyl-2(1H)-quinolinone | HCID 10086884 | 81% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05310914 |
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| Source dataset | uspto-grants-1994_05 |
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| ORD ID | ord-93adbae73078457caa96daf3e022cf96 |
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| Source note | uspto-grants-1994_05 |
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