Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2423506Generated: November 3, 2026

Water → Ethyl 6-[4-({[3-(2,6-dichlorophenyl)-5-(1-methylethyl)-4-isoxazolyl]methyl}oxy)phenyl]-3-methyl-2-quinolinecarboxylate

https://huagongshe.com/reaction/2423506

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantCesium carbonateHCID 10796—
Reactant4-(Chloromethyl)-3-(2,6-dichlorophenyl)-5-isopropylisoxazoleHCID 59264875—
ReactantEthyl 6-(4-hydroxyphenyl)-3-methyl-2-quinolinecarboxylateHCID 59321543—
SolventDimethylformamideHCID 6228—
ProductEthyl 6-[4-({[3-(2,6-dichlorophenyl)-5-(1-methylethyl)-4-isoxazolyl]methyl}oxy)phenyl]-3-methyl-2-quinolinecarboxylateHCID 5932151544%

Reaction Steps

Cesium carbonate (71.7 mg, 220.1 μmol) was added to ethyl 6-(4-hydroxyphenyl)-3-methyl-2-quinolinecarboxylate (61.5 mg, 200.1 μmol) and 4-(chloromethyl)-3-(2,6-dichlorophenyl)-5-(1-methylethyl)isoxazole (67.0 mg, 220.1 μmol) in N,N-dimethylformamide (4 mL) at room temperature. The resulting suspension was stirred for 18 hours, then water was added and the reaction mixture was extracted with ethyl acetate. The organic layer was dried over anhydrous magnesium sulfate, then filtered and concentrated. The residue was purified by silica gel chromatography eluting with 3:7 ethyl acetate:hexanes to give 50.7 mg (44%) of ethyl 6-[4-({[3-(2,6-dichlorophenyl)-5-(1-methylethyl)-4-isoxazolyl]methyl}oxy)phenyl]-3-methyl-2-quinolinecarboxylate as an oil. 1H NMR (400 MHz, d6-DMSO): δ 8.32 (s, 1H), 8.14 (s, 1H), 8.08-8.01 (m, 2H), 7.72 (s, 1H), 7.70 (s, 1H), 7.63 (d, J=8 Hz, 2H), 7.55 (dd, J=9, 7 Hz, 1H), 6.93 (d, J=9 Hz, 2H), 4.89 (s, 2H), 4.41 (q, J=7 Hz, 2H), 3.48 (septet, J=7 Hz, 1H), 2.55 (s, 3H), 1.36 (t, J=7 Hz, 3H), 1.34 (d, J=7 Hz, 6H). ESI-LCMS m/z 575 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07960552B2
Source datasetuspto-grants-2011_06
ORD IDord-ba2afd5ec03c442eae52d29e5b276db6
Source noteuspto-grants-2011_06