Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1497329Generated: October 30, 2026

Toluene → Ethyl 4-[(2-methoxypyridin-4-yl)methyl]quinoline-2-carboxylate

https://huagongshe.com/reaction/1497329

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantSodium CarbonateHCID 10340—
Reactant4-(Bromomethyl)-2-methoxypyridineHCID 19805431—
ReactantEthyl 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)quinoline-2-carboxylateHCID 60209908—
CatalystHCID 178418397HCID 178418397—
SolventEthanolHCID 702—
ProductEthyl 4-[(2-methoxypyridin-4-yl)methyl]quinoline-2-carboxylateHCID 60209910—

Reaction Conditions

Temperature85 °C

Reaction Steps

In a microwave vial containing ethyl 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)quinoline-2-carboxylate (K4) (0.23 g, 0.69 mmol), 4-(bromomethyl)-2-methoxypyridine (M3) (0.17 g, 0.83 mmol), and palladium tetrakis (0.52 g, 0.45 mmol) was, added 4.0 mL toluene, 2.8 mL, ethanol, and 1.0 mL 2.0 M aqueous Na2CO3. The resulting solution was heated to 85° C. for 30 minutes, filtered through Celite, and washed with excess ethyl acetate. The filtrate was washed twice with water, washed with brine, dried over sodium sulfate, filtered, and concentrated. The resultant residue was subjected to silica gel chromatography eluting with 0-100% ethyl acetate in hexanes to afford ethyl 4-[(2-methoxypyridin-4-yl)methyl]quinoline-2-carboxylate (M4) that gave a mass ion (ES+) of 323.3 for M+H+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09199939B2
Source datasetuspto-grants-2015_12
ORD IDord-1873c5c5645b4401a0c903f6976f9d9e
Source noteuspto-grants-2015_12