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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1911755Generated: November 3, 2026

Acetic Acid → 3-((3,5-bis(trifluoromethyl)benzylamino)methyl)-N,N-bis(cyclopropylmethyl)-8-methylquinolin-2-amine

https://huagongshe.com/reaction/1911755

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
Reactant3,5-Bis(trifluoromethyl)benzylamineHCID 521099—
ReactantSodium cyanoborohydrideHCID 5003444—
Reactant2-(Bis(cyclopropylmethyl)amino)-8-methylquinoline-3-carbaldehydeHCID 57486822—
SolventMethanolHCID 887—
Product3-((3,5-bis(trifluoromethyl)benzylamino)methyl)-N,N-bis(cyclopropylmethyl)-8-methylquinolin-2-amineHCID 5748682399%

Reaction Steps

2-(Bis(cyclopropylmethyl)amino)-8-methylquinoline-3-carbaldehyde (0.081 g, 0.39 mmol), 3,5-bis-trifluoromethylbenzylamine (0.096 g, 0.39 mmol) and acetic acid (0.047 g, 0.78 mmol) were put in a 25 mL RB flask. To this, 2 mL of methanol was added and stirred at RT for 15 min. Sodium cyanoborohydride (0.075 g, 0.77 mmol) was added portionwise and stirring was continued at RT for another 1 h. Methanol was removed from the reaction mixture under vacuum, water was added to this crude and was extracted with ethyl acetate (3×50 mL). The organic layer was washed with saturated NaHCO3 solution, brine and dried over sodium sulphate. The solvent was evaporated and the crude residue was purified by column chromatography over silica gel (100-200 mesh) eluting with 4% ethyl acetate in petroleum ether to give the title amine (0.142 g, yield: 99%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08604055B2
Source datasetuspto-grants-2013_12
ORD IDord-4f9d2306faf24743a2e5e544bd799407
Source noteuspto-grants-2013_12