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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 590048Generated: October 30, 2026

Pyridine → Methyl 3-(2,5-difluorophenylsulfonamido)-4-fluorobenzoate

https://huagongshe.com/reaction/590048

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
Reactant2,5-Difluorobenzenesulfonyl chlorideHCID 2736911—
ReactantMethyl 3-amino-4-fluorobenzoateHCID 12541234—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
ProductMethyl 3-(2,5-difluorophenylsulfonamido)-4-fluorobenzoateHCID 3349350094.5%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of methyl 3-amino-4-fluorobenzoate (25 g, 149 mmol) in DCM (150 mL) were added pyridine (35.3 g, 446 mmol) and a catalytic amount of DMAP (1.8 g, 14.9 mmol). The mixture was cooled to 0° C. 2,5-Difluorobenzene-1-sulfonyl chloride (34.7 g, 212 mmol) in DCM (20 mL) was added dropwise to the mixture. The reaction was stirred at rt overnight. Then the reaction was washed with water (300 mL), and extracted with DCM (2×400 mL). The organic layer was washed with brine, dried over anhydrous NaSO4, filtrated and concentrated under reduced pressure to give the crude product, which was washed with petroleum ether to afford the title compound of Step A (48.2 g, 94.5% yield). 1H NMR (400 MHz, CDCl3) δ ppm 8.12-8.18 (m, 1H), 7.73-7.80 (m, 1H), 7.47-7.53 (m, 1H), 7.10-7.25 (m, 1H), 7.00-7.07 (m, 1H), 3.86 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09233956B2
Source datasetuspto-grants-2016_01
ORD IDord-b36bff53d34e48e1bb97f0203ea14bc2
Source noteuspto-grants-2016_01