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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2423525Generated: November 2, 2026

Hydrochloric Acid → HCID 59321574, compound

https://huagongshe.com/reaction/2423525

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantWaterHCID 962—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 59321567HCID 59321567—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
ProductHCID 59321574HCID 5932157499%

Reaction Conditions

Temperature90 °C

Reaction Steps

A 1 N solution of sodium hydroxide (92.8 μL, 92.8 μmol) was added to ethyl 6-[4-({[3-(2,6-dichlorophenyl)-5-(1-methylethyl)-4-isoxazolyl]methyl}oxy)phenyl]-2-methyl-3-quinolinecarboxylate (26.7 mg, 46.4 μmol) in tetrahydrofuran and methanol (1:1, 927.9 μL) and the mixture was heated in the microwave at 90° C. for 10 minutes. After cooling, the mixture was neutralized with 1 N hydrochloric acid (92.8 μL), water was added, and the reaction mixture was extracted with ethyl acetate. The organic layer was washed with brine, then dried over anhydrous magnesium sulfate, filtered and concentrated to give 25.1 mg (99%) of 6-[4-({[3-(2,6-dichlorophenyl)-5-(1-methylethyl)-4-isoxazolyl]methyl}oxy)phenyl]-2-methyl-3-quinolinecarboxylic acid as a solid. 1H NMR (400 MHz, d6-DMSO): δ 13.31 (br s, 1H), 8.86 (s, 1H), 8.29 (d, J=2 Hz, 1H), 8.09 (dd, J=9, 2 Hz, 1H), 7.98 (d, J=9 Hz, 1H), 7.69 (d, J=9 Hz, 2H), 7.66-7.60 (m, 2H), 7.55 (dd, J=9, 7 Hz, 1H), 6.93 (d, J=9 Hz, 2H), 4.88 (s, 2H), 3.47 (septet, J=7 Hz, 1H), 2.86 (s, 3H), 1.34 (d, J=7 Hz, 6H). HRMS C30H24Cl2N2O4 m/z 547.1191 (M+H)+Cal; 547.1191 (M+H)+Obs.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07960552B2
Source datasetuspto-grants-2011_06
ORD IDord-b64c013f8b69405cb6d5405da59b20c4
Source noteuspto-grants-2011_06