HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2080671Generated: October 30, 2026
Potassium Nitrate → Methyl 5-[4-(ethylsulfonyl)phenoxy]-3-nitro-2-[(2-pyridinylcarbonyl)amino]benzoate
https://huagongshe.com/reaction/2080671
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Nitrate | HCID 24434 | — |
| Reactant | Methyl 5-[4-(ethylsulfonyl)phenoxy]-2-[(2-pyridinylcarbonyl)amino]benzoate | HCID 67110490 | — |
| Solvent | Trifluoroacetic acid | HCID 6422 | — |
| Product | Methyl 5-[4-(ethylsulfonyl)phenoxy]-3-nitro-2-[(2-pyridinylcarbonyl)amino]benzoate | HCID 57433575 | 88.8% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07932394B2 |
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| Source dataset | uspto-grants-2011_04 |
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| ORD ID | ord-5a1badcb29694e3588546adb8b82feb8 |
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| Source note | uspto-grants-2011_04 |
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