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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1961748Generated: October 30, 2026

Pyridine → 3-(2,5-Difluoro-benzenesulfonylamino)-2-fluoro-benzoic acid methyl ester

https://huagongshe.com/reaction/1961748

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
Reactant2,5-Difluorobenzenesulfonyl chlorideHCID 2736911—
ReactantMethyl 3-amino-2-fluorobenzoateHCID 46311080—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
Product3-(2,5-Difluoro-benzenesulfonylamino)-2-fluoro-benzoic acid methyl esterHCID 58316996—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of methyl 3-amino-2-fluorobenzoate (21.8 g, 129 mmol) in DCM (300 mL) were added pyridine (30.6 g, 387.6 mmol) and a catalytic amount of DMAP. The mixture was cooled to 0° C. 2,5-Difluorobenzene-1-sulfonyl chloride (28.8 g, 136 mmol) in DCM (20 mL) was added dropwise to the mixture. The reaction was stirred at rt overnight. The reaction mixture was washed with water (300 mL), and extracted with DCM (2×200 mL). The organic layer was washed with brine, dried over anhydrous NaSO4, filtered and concentrated under reduced pressure to give the crude product, which was washed with petroleum ether to afford the title compound of Step A. (16 g, 35.9%). 1H NMR (400 MHz, DMSO-d6) δ ppm 10.71-10.91 (br, 1H), 7.65-7.73 (m, 1H), 7.48-7.62 (m, 4H), 7.20-7.28 (m, 1H), 3.77 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08415345B2
Source datasetuspto-grants-2013_04
ORD IDord-f079ba2c9d0244c880503aab21dc0c8d
Source noteuspto-grants-2013_04