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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2080671Generated: October 31, 2026

Potassium Nitrate → Methyl 5-[4-(ethylsulfonyl)phenoxy]-3-nitro-2-[(2-pyridinylcarbonyl)amino]benzoate

https://huagongshe.com/reaction/2080671

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium NitrateHCID 24434—
ReactantMethyl 5-[4-(ethylsulfonyl)phenoxy]-2-[(2-pyridinylcarbonyl)amino]benzoateHCID 67110490—
SolventTrifluoroacetic acidHCID 6422—
ProductMethyl 5-[4-(ethylsulfonyl)phenoxy]-3-nitro-2-[(2-pyridinylcarbonyl)amino]benzoateHCID 5743357588.8%

Reaction Conditions

Temperature80 °C

Reaction Steps

1.9 g of methyl 5-[4-(ethylsulfonyl)phenoxy]-2-[(2-pyridinylcarbonyl)amino]benzoate was dissolved in 20 ml of trifluoroacetic acid, and 2.2 g of potassium nitrate was added to it and stirred under heat at 80° C. for 2 hours. The reaction liquid was restored to room temperature, trifluoroacetic acid was evaporated away under reduced pressure, the residue was dissolved in chloroform, and aqueous saturated sodium hydrogencarbonate solution was added to it. This was extracted with chloroform, and the organic layer was washed with saturated saline water. After dried, the solvent was evaporated away under reduced pressure, and the residue was purified through silica gel column chromatography (developing solvent: hexane/ethyl acetate=2/1 to 1/1) to obtain 1.86 g of the entitled compound as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07932394B2
Source datasetuspto-grants-2011_04
ORD IDord-5a1badcb29694e3588546adb8b82feb8
Source noteuspto-grants-2011_04