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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 625333Generated: October 30, 2026

Sodium ethanethiolate → HCID 66586843, compound

https://huagongshe.com/reaction/625333

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ethanethiolateHCID 4459711—
ReactantN-(3-(trifluoromethyl)benzyl)-2-(5-fluoro-2-nitrophenyl)-isonicotinamideHCID 66586802—
SolventDimethyl SulfoxideHCID 679—
ProductHCID 66586843HCID 66586843—

Reaction Conditions

Temperature90 °C

Reaction Steps

Into a 50-mL round-bottom flask, was placed a solution of N-(3-(trifluoromethyl)benzyl)-2-(5-fluoro-2-nitrophenyl)isonicotinamide 14d (300 mg, 0.72 mmol, 1.00 equiv) in DMSO (5 mL), and sodium ethanethiolate (100 mg, 1.19 mmol, 1.70 equiv). The resulting solution was stirred for overnight at 90° C. in an oil bath. The mixture was concentrated under vacuum. The residue was diluted with 20 mL of water. The resulting solution was extracted with 3×20 mL of dichloromethane and the organic layers combined. The mixture was dried over anhydrous sodium sulfate and concentrated under vacuum. This resulted in 300 mg (crude) of N-(3-(trifluoromethyl)benzyl)-2-(5-(ethylthio)-2-nitrophenyl)isonicotinamide as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09301951B2
Source datasetuspto-grants-2016_04
ORD IDord-f46b3e0c82a747d0943b3ee1dacd1642
Source noteuspto-grants-2016_04