Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 419116Generated: October 30, 2026

HCID 46318655, compound → HCID 57942367, compound

https://huagongshe.com/reaction/419116

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 46318655HCID 46318655—
ReactantN-(2-Bromo-5-chloro-pyridin-3-yl)-4-chloro-N-methoxvmethyl-3-trifluoromethyl-benzenesulfonamideHCID 57942086—
ReactantHCID 178418918HCID 178418918—
SolventTetrahydrofuranHCID 8028—
ProductHCID 57942367HCID 5794236760.2%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of N-(2-Bromo-5-chloro-pyridin-3-yl)-4-chloro-N-methoxymethyl-3-trifluoromethyl-benzenesulfonamide (250 mg, 0.50 mmol) in 4.0 ml of THF under nitrogen atmosphere at 0° C. was added drop-wise 0.6 mLl (1.2 mmol) of isopropylmagnesium chloride. The mixture was then stirred for 20 min at 0° C. followed by addition of a solution of 2-Bromo-N-methoxy-N-methyl-benzamide (244 mg, 1.0 mmol) in 1 mL of THF. The mixture was stirred at room temperature overnight, quenched with saturated ammonium chloride and extracted with ethyl acetate. After concentration of the solvent the residue was purified by flash chromatograph (20% ethyl acetate in hexane) to afford 180 mg of title compound as an off white solid. MS: (M+Na)/z=621.2, (M-32)/z=567.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08093247B2
Source datasetuspto-grants-2012_01
ORD IDord-5186781b40c34456bb33a9eb94725457
Source noteuspto-grants-2012_01