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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1961765Generated: October 31, 2026

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

https://huagongshe.com/reaction/1961765

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 numberUS08415345B2
Source datasetuspto-grants-2013_04
ORD IDord-acf060116f7643b68222954a22aae204
Source noteuspto-grants-2013_04