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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1385952Generated: November 1, 2026

HCID 15457194, compound → HCID 18408351, compound

https://huagongshe.com/reaction/1385952

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 15457194HCID 15457194—
CatalystCopperHCID 23978—
SolventQuinolineHCID 7047—
ProductHCID 18408351HCID 1840835170.4%

Reaction Conditions

Temperature210 °C

Reaction Steps

0.29 g (0.74 mmol) of 3-(2-carboxy-7-chloro-5-fluorobenzofuran-4-yl)-1-methyl-6-trifluoromethyl-2-(1H)-pyridone was dissolved in 15 ml of quinoline, and 0.05 g (0.75 mmol) of copper powder was added thereto, followed by stirring at 210° C. for 15 minutes. Then, copper was removed by filtration, and the filtrate was poured into water and acidified by an addition of hydrochloric acid, and then extracted with ethyl acetate. After washing with water, the organic layer was dried over anhydrous magnesium sulfate. Ethyl acetate was distilled off under reduced pressure. Then, the obtained residue was purified by silica gel column chromatography to obtain 0.18 g (yield: 70%) of the desired product. Melting point: 178-179° C. 1H-NMR (300 MHz, CDCl3) δ value: 3.74(3H,s), 6.66(1H,d), 6.81(1H,d), 7.20(1H,d), 7.56(1H,d), 7.72(1H,d)ppm.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06265349B1
Source datasetuspto-grants-2001_07
ORD IDord-7a87ad0c3b58486494737334342eb2b5
Source noteuspto-grants-2001_07