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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1949176Generated: October 31, 2026

Methanol → HCID 59486218, compound

https://huagongshe.com/reaction/1949176

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantHexaneHCID 8058—
ReactantSodiumHCID 5360545—
ReactantHCID 59486210HCID 59486210—
ProductHCID 59486218HCID 5948621838%

Reaction Conditions

Temperature60 °C

Reaction Steps

20 mg (0.95 mmol) sodium were added to methanol (6 ml) at RT. Once the sodium had completely dissolved, a solution of 210 mg (0.47 mmol) 4-chloro-2-ethylsulfanyl-N-[(3-fluorophenyl)-methyl]-7-(trifluoromethyl)-quinoline-3-carboxamide (example 122) in MeOH (2 ml) was added at RT. The mixture was then heated for 30 min at 60° C. Then the mixture was concentrated to small volume under vacuum and the residue was taken up with water and extracted with EE. The organic phase was washed with water and brine, dried over Na2SO4, filtered and concentrated to small volume under vacuum. Column chromatography (hexane/EE 9:1) of the residue yielded 80 mg (0.18 mmol, 38%) 2-ethylsulfanyl-N-[(3-fluorophenyl)-methyl]-4-methoxy-7-(trifluoromethyl)-quinoline-3-carboxamide. MS: m/z 439.1 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08399673B2
Source datasetuspto-grants-2013_03
ORD IDord-ec91a1ecf3604583a9b33559c52801bb
Source noteuspto-grants-2013_03