Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1944610Generated: November 1, 2026

Sodium Bicarbonate → Methyl 1-(4-(6-bromo-3-nitroquinolin-4-ylamino)-2-(trifluoromethyl)phenyl)piperidine-4-carboxylate

https://huagongshe.com/reaction/1944610

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium BicarbonateHCID 516892—
Reactant6-Bromo-4-chloro-3-nitroquinolineHCID 21984128—
ReactantMethyl 1-(4-amino-2-(trifluoromethyl)phenyl)piperidine-4-carboxylateHCID 67007713—
SolventEthyl AcetateHCID 8857—
Solvent1,4-DioxaneHCID 31275—
ProductMethyl 1-(4-(6-bromo-3-nitroquinolin-4-ylamino)-2-(trifluoromethyl)phenyl)piperidine-4-carboxylateHCID 6700814890.4%

Reaction Steps

To a solution of compound 8.0 6-bromo-4-chloro-3-nitroquinoline (0.29 g, 1.0 mmol, 1 equiv.) in dioxane (5 mL) at room temperature was added 8.1 methyl 1-(4-amino-2-(trifluoromethyl)phenyl)piperidine-4-carboxylate (0.3 g, 1.0 mmol, 1 equiv.). The resulting mixture was heated overnight to 85° C. under argon. Upon cooling to room temperature, the mixture was neutralized with aqueous NaHCO3, diluted with EtOAc (50 mL), and washed with water (50 mL) and brine (50 mL). The organic phase was dried over Na2SO4. After removal of solvent under vacuum, the resulting residue was purified via flash chromatography (Hexanes: EtOAc=4:1) to afford desired product 8.2 methyl 1-(4-(6-bromo-3-nitroquinolin-4-ylamino)-2-(trifluoromethyl)phenyl)piperidine-4-carboxylate (0.50 g; 90%). LC-MS (M+H): 555.10

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08394818B2
Source datasetuspto-grants-2013_03
ORD IDord-b450ac1881504b86af534a3beee8172f
Source noteuspto-grants-2013_03