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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1913730Generated: November 1, 2026

Pyridine → HCID 66879858, compound

https://huagongshe.com/reaction/1913730

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
Reactant1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
Reactant3-Fluoropyridine-4-carboxylic acidHCID 345361—
ReactantHCID 58148233HCID 58148233—
SolventWaterHCID 962—
ProductHCID 66879858HCID 6687985862.7%

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of 1.5 g of 6-amino-1,1,3,3-tetrafluoro-5-hydroxy-1,3-dihydroisobenzofuran, 0.95 g of 3-fluoroisonicotinic acid, 1.68 g of WSC and 13 ml of pyridine was stirred while heating at 80° C. for two hours. The reaction mixture was cooled to room temperature, and then water was added, followed by extraction with ethyl acetate three times. The combined organic layers were washed with water and a saturated sodium chloride solution, dried over anhydrous magnesium sulfate, and then concentrated under reduced pressure. The residue was subjected to silica gel column chromatography to give 1.46 g of 3-fluoro-N-(1,1,3,3-tetrafluoro-6-hydroxy-1,3-dihydroisobenzofuran-5-yl)isonicotinamide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08609705B2
Source datasetuspto-grants-2013_12
ORD IDord-e0bd6cd7701d47ddab592f6c3d5b6f88
Source noteuspto-grants-2013_12