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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 917699Generated: October 30, 2026

Pyridine → HCID 23631099, compound

https://huagongshe.com/reaction/917699

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantPentafluorophenyl TrifluoroacetateHCID 4327891—
Reactant4-(2-Fluoro-4-iodoanilino)-1-methyl-6-oxo-1,6-dihydro-3-pyridinecarboxylic acidHCID 11234608—
SolventEthyl AcetateHCID 8857—
SolventDimethylacetamideHCID 31374—
ProductHCID 23631099HCID 23631099—

Reaction Steps

4-(2-Fluoro-4-iodoanilino)-1-methyl-6-oxo-1,6-dihydro-3-pyridinecarboxylic acid (894 mg, 2.30 mmol) and pyridine (909 mg, 11.5 mmol) were dissolved in DMA (15 mL). To this mixture was added pentafluorophenyl trifluoroacetate (3.22 g, 11.5 mmol) then the solution was allowed to stir at R.T. for 2 h. The DMA solution was diluted with EtOAc (150 mL), which was washed sequentially with 1 M HCl (2×100 mL), water (100 mL), sat. NaHCO3 (2×100 mL), and brine (100 mL). The EtOAc fraction was then dried (Na2SO4) and the solvent removed under reduced pressure to yield a viscous oil which was purified by column chromatography on silica gel (50% EtOAc/PE as eluant). This afforded 2,3,4,5,6-pentafluorophenyl-4-(2-fluoro-4-iodoanilino)-1-methyl-6-oxo-1,6-dihydro-3-pyridinecarboxylate as a cream foam (1.22 g, 96%) which was used directly in subsequent steps. 1H NMR [(CD3)2SO, 400 MHz] δ 9.03 (s, 1H), 8.70 (s, 1H), 7.79 (dd, J=10.1, 1.9 Hz, 1H), 7.62 (br dd, J=8.4, 1.0 Hz, 1H), 7.29 (t, J=8.4 Hz, 1H), 5.36 (d, J=1.6 Hz, 1H), 3.45 (s, 3H). LCMS (APCI+) calcd for C19H9F6N2O3 555 (MH+), found 555.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07273877B2
Source datasetuspto-grants-2007_09
ORD IDord-7e7dc2d8cfb3478781a7ecd2dc22155d
Source noteuspto-grants-2007_09