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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 448117Generated: October 30, 2026

3-(Methylthio)propanoic acid → 4-tert-butyl-N-{4-chloro-5-fluoro-2-[N'-(3-methylsulfanyl-propionyl)-hydrazinocarbonyl]-phenyl}-benzenesulfonamide

https://huagongshe.com/reaction/448117

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-(Methylthio)propanoic acidHCID 563—
ReactantTriethylamineHCID 8471—
ReactantOxalyl chlorideHCID 65578—
Reactant4-tert-butyl-N-(4-chloro-5-fluoro-2-hydrazinocarbonyl-phenyl)-benzenesulfonamideHCID 59302966—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
Product4-tert-butyl-N-{4-chloro-5-fluoro-2-[N'-(3-methylsulfanyl-propionyl)-hydrazinocarbonyl]-phenyl}-benzenesulfonamideHCID 59303041—

Reaction Steps

To a stirred solution of 3-methylsulfanyl-propionic acid (120 mg, 1.0 mmol) under an inert atmosphere in 6 mL of anhydrous DCM and DMF (200 μL) was added oxalyl chloride (89 μL, 1.0 mmol). The resultant solution was stirred at room temperature overnight and then added to a solution of 4-tert-butyl-N-(4-chloro-5-fluoro-2-hydrazinocarbonyl-phenyl)-benzenesulfonamide (400 mg, 1.0 mmol) and Et3N (0.35 mL, 2.5 mmol) at 0° C. The resultant solution was stirred at room temperature for 4 hours and the solvent was removed in vacuo. The residue was purified via automated silica gel chromatography to afford 4-tert-butyl-N-{4-chloro-5-fluoro-2-[N′-(3-methylsulfanyl-propionyl)-hydrazinocarbonyl]-phenyl}-benzenesulfonamide as an oil: MS (ES) M+H expected 502.1, found 502.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08481579B2
Source datasetuspto-grants-2013_07
ORD IDord-bde5ac37ac86412b9ad8f533754c68b2
Source noteuspto-grants-2013_07