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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1352489Generated: October 25, 2026

Benzylamine → 2-Methyl-4-benzylimino-3,4-dihydro-2H-quinoline-1-carboxylic acid benzyl ester

https://huagongshe.com/reaction/1352489

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzylamineHCID 7504—
ReactantTriethylamineHCID 8471—
Reactant2-Methyl-4-oxo-3,4-dihydro-2H-quinoline-1-carboxylic Acid Benzyl EsterHCID 12093186—
CatalystTitanium TetrachlorideHCID 24193—
SolventTolueneHCID 1140—
SolventDichloromethaneHCID 6344—
Product2-Methyl-4-benzylimino-3,4-dihydro-2H-quinoline-1-carboxylic acid benzyl esterHCID 69429875130.4%

Reaction Steps

To a solution of 2-Methyl-4-oxo-3,4-dihydro-2H-quinoline-1-carboxylic acid benzyl ester (1.00 g, 3.39 mmol), triethylamine (3.77 mL, 27.1 mmol) in dichloromethane (10 ml), cooled at 0° C. in an ice/sodium chloride bath, a solution of titanium tetrachloride in toluene (3.39 mL, 1.0 M in toluene) was dropwise added for 10 minutes. Benzyl amine (0.74 mL, 3.39 mmol) was added and the mixture was stirred over night at room temperature. The reaction was quenched with saturated NaHCO3 solution (100 mL) and the mixture was extracted with ethyl acetate (3×200 mL). The combined organic layers were washed with brine (200 mL), dried (Na2SO4), filtered and concentrated to give a reddish oil (1.70 g) which was used directly in the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07220760B2
Source datasetuspto-grants-2007_05
ORD IDord-67bb2411fd734d7397eb96c04938e382
Source noteuspto-grants-2007_05