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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1363039Generated: October 28, 2026

Carbon Dioxide → 4-Chloro-2-(4-chloro-3-trifluoromethyl-benzenesulfonylamino)-N-methoxy-N-methyl-benzamide

https://huagongshe.com/reaction/1363039

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon DioxideHCID 280—
ReactantWaterHCID 962—
ReactantMethanamine, N-methoxy-, hydrochloride (1:1)HCID 81138—
Reactant4-Chloro-2-[4-chloro-3-(trifluoromethyl)benzenesulfonamido]benzoic acidHCID 2128678—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
Product4-Chloro-2-(4-chloro-3-trifluoromethyl-benzenesulfonylamino)-N-methoxy-N-methyl-benzamideHCID 5787080173%

Reaction Steps

To a solution of 4-chloro-2-(4-chloro-3-trifluoromethyl-benzenesulfonylamino)-benzoic acid (5.0 g, 12.1 mmol) in THF (20 mL) was added N,N′-carbonyldiimidazole (CDI, 2.45 g, 15.13 mmol) in portions (Caution!: CO2↑). The resulting reaction mixture was then heated at reflux. After 4 hours, reaction mixture was cooled to room temperature and charged with N,O-dimethylhydroxylamine hydrochloride (1.3 g, 13.31 mmol) and heated at reflux for 1 hour. Water (100 mL) was added followed by EtOAc (100 mL) with stirring. EtOAc layer was separated and aqueous layer was further extracted with EtOAc (2×50 mL). Combined EtOAc layers were washed with aq. 2N HCl (50 mL), saturated NaHCO3 solution (50 mL), brine (50 mL), dried (Na2SO4) and evaporated. Obtained crude product was purified by automated normal-phase chromatography (50% EtOAc in hexanes) to afford title compound (4.0 g) in 73% yield. MS (ES) M+H expected 457.0, found 456.9.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07884110B2
Source datasetuspto-grants-2011_02
ORD IDord-1c3a3a6db60b4cb7a7d5c8982007387f
Source noteuspto-grants-2011_02