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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1716645Generated: October 29, 2026

Methylamine hydrochloride → HCID 59831817, compound

https://huagongshe.com/reaction/1716645

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethylamine hydrochlorideHCID 6364545—
ReactantTrimethylaluminumHCID 16682925—
Reactant3-(1H-Indol-6-yl)-3-(4-methoxy-phenyl)-propionic acid methyl esterHCID 59831611—
SolventBenzeneHCID 241—
ProductHCID 59831817HCID 5983181781%

Reaction Conditions

Temperature5 °C

Reaction Steps

To a 5° C. stirring suspension of MeNH2.HCl (220 mg, 3.2 mmol) in benzene (3 ml) was added dropwise Me3Al (2 M in toluene, 1.6 ml, 3.2 mmol). The mixture was stirred at room temperature for 45 minutes. A solution of 3-(1H-indol-6-yl)-3-(4-methoxy-phenyl)-propionic acid methyl ester XXXIV (480 mg, 1.6 mmol) in benzene (15 ml) was added and the resulting mixture was stirred at reflux for 3 hours. The reaction mixture was cooled to room temperature and additional mixture of MeNH2.HCl (110 mg, 1.6 mmol) in benzene (1.5 ml) and Me3Al (2M in toluene, 0.8 ml, 1.6 mmol) was added. The resulting mixture was stirred at reflux for 1.5 hours, cooled to room temperature, and the reaction was quenched by slow addition of HCl (1M, 35 ml). The mixture was stirred vigorously for 5 minutes and extracted with EtOAc (50 ml). The combined organic layers were washed with water and brine, dried over MgSO4, filtered, concentrated and purified via flash chromatography (hexane/EtOAc) to provide 3-(1H-indol-6-yl)-3-(4-methoxy-phenyl)-N-methyl-propionamide XXXV (390 mg, 81% yield) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07803830B2
Source datasetuspto-grants-2010_09
ORD IDord-0679052d49cd457084d84a1836d3150e
Source noteuspto-grants-2010_09