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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2093725Generated: November 1, 2026

Hydrochloric Acid → 2-((Dimethylamino)methyl)-4-methyl-7-(trifluoromethyl)quinoline-3-carboxylic acid ethyl ester

https://huagongshe.com/reaction/2093725

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantDiisopropylethylamineHCID 81531—
ReactantEthyl 3-chloro-3-oxopropionateHCID 118931—
ReactantDimethylazanium;chlorideHCID 12954980—
Reactant1-(2-Amino-4-(trifluoromethyl)phenyl)ethan-1-oneHCID 46835500—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
SolventEthyl AcetateHCID 8857—
Product2-((Dimethylamino)methyl)-4-methyl-7-(trifluoromethyl)quinoline-3-carboxylic acid ethyl esterHCID 6658400946%

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of 1.0 g (5.0 mmol) 1-(2-amino-4-(trifluoromethyl)phenyl)ethanone, 3.4 ml (25.0 mmol) ethyl 3-chloro-3-oxopropanoate and 435 μl (5.0 mmol) conc. hydrochloric acid was heated in a sealed vessel in the MW to 100° C. for 30 min. The mixture was subsequently diluted with EtOAc and water. The organic phase was separated, washed with a 1M aq. NaHCO3 sol., dried over MgSO4 and concentrated in a vacuum. The raw product (1.14 g) obtained after CC (EtOAc/hexane 3:17) of the residue was dissolved in MeCN (6 ml) and 2.7 ml (15.5 mmol) DIPEA and 838 mg (10.3 mmol) dimethylammoniumchlorid were added. The mixture was subsequently stirred at RT for 16 h. After cooling to RT, the mixture was diluted with water and extracted with EtOAc. The organic layer was extracted twice a 2N aq. HCl and water. The combined aqueous layers were basified with Na2CO3 and extracted with EtOAc. The organic layer was washed with brine, dried over MgSO4 and concentrated in vacuum. As residue 776 mg (2.3 mmol, 46%) 2-((dimethylamino)methyl)-4-methyl-7-(trifluoromethyl)quinoline-3-carboxylic acid ethyl ester was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08445512B2
Source datasetuspto-grants-2013_05
ORD IDord-cb751411734e4e15bc8e6149687e5272
Source noteuspto-grants-2013_05