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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1670941Generated: October 30, 2026

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

https://huagongshe.com/reaction/1670941

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 numberUS07994185B2
Source datasetuspto-grants-2011_08
ORD IDord-7469b313ec5f40d0b911256c3ab0863c
Source noteuspto-grants-2011_08