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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 926547Generated: October 30, 2026

(4-Chloro-2-methoxy-3-(4-(trifluoromethyl)benzyl)quinolin-6-yl)(3,5-dimethylisoxazol-4-yl)methanol → (4-Chloro-2-methoxy-3-(4-(trifluoromethyl)benzyl)quinolin-6-yl)(3,5-dimethylisoxazol-4-yl)methanone

https://huagongshe.com/reaction/926547

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(4-Chloro-2-methoxy-3-(4-(trifluoromethyl)benzyl)quinolin-6-yl)(3,5-dimethylisoxazol-4-yl)methanolHCID 118005804—
CatalystHCID 178418406HCID 178418406—
SolventTetrahydrofuranHCID 8028—
Product(4-Chloro-2-methoxy-3-(4-(trifluoromethyl)benzyl)quinolin-6-yl)(3,5-dimethylisoxazol-4-yl)methanoneHCID 118006246—

Reaction Steps

To a flask containing (4-chloro-2-methoxy-3-(4-(trifluoromethyl)benzyl)quinolin-6-yl)(3,5-dimethylisoxazol-4-yl)methanol (1.4 g, 2.94 mmol, Intermediate 63: step a) was added THF (75 mL) followed by manganese dioxide (1.1 g, 12.6 mmol). The reaction mixture was heated to reflux for 2 hours, and then the contents were filtered through Celite® and rinsed with additional THF. The effluent was concentrated to provide the title compound as a white amorphous solid which was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09284308B2
Source datasetuspto-grants-2016_03
ORD IDord-34429e885cc243e185a3091da710427a
Source noteuspto-grants-2016_03