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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1009763Generated: October 26, 2026

4,5-Dimethylisoxazol-3-amine → N-(4,5-dimethylisoxazol-3-yl)-2-[4-(6-fluoroquinolin-4-yloxy)-2-methoxyphenyl]propionamide

https://huagongshe.com/reaction/1009763

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4,5-Dimethylisoxazol-3-amineHCID 84148—
Reactant2-[4-(6-Fluoroquinolin-4-yloxy)-2-methoxyphenyl]propionic acidHCID 67304950—
ProductN-(4,5-dimethylisoxazol-3-yl)-2-[4-(6-fluoroquinolin-4-yloxy)-2-methoxyphenyl]propionamideHCID 6730405911%

Reaction Steps

Using an analogous procedure to that described in Example 2, 2-[4-(6-fluoroquinolin-4-yloxy)-2-methoxyphenyl]propionic acid was reacted with 3-amino-4,5-dimethylisoxazole. The resultant mixture was evaporated and the residue was purified by preparative HPLC using a Waters ‘Xterra’ reversed-phase column (5 microns silica, 30 mm diameter, 150 mm length) using decreasingly polar mixtures of water (containing 0.2% ammonium carbonate) and acetonitrile as eluent. There was thus obtained the title compound as a solid in 11% yield; 1H NMR: (DMSOd6) 1.43 (s, 3H), 1.77 (s, 3H), 2.3 (s, 3H), 3.81 (s, 3H), 4.16 (q, 1H), 6.72 (d, 1H), 6.87 (m, 1H), 7.0 (d, 1H), 7.4 (d, 1H), 7.75 (m, 1H), 7.97 (m, 1H), 8.12 (m, 1H), 8.7 (d, 1H), 10.16 (s, 1H); Mass Spectrum: M+H+ 436.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07973164B2
Source datasetuspto-grants-2011_07
ORD IDord-a8bed9d616ad4ff2bf4678bb1dc2b16e
Source noteuspto-grants-2011_07