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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1391503Generated: October 30, 2026

Chloride → HCID 67313333, compound

https://huagongshe.com/reaction/1391503

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorideHCID 312—
Reactant3-PyridinecarboxaldehydeHCID 10371—
Reactant2-Iodosylbenzoic acidHCID 67537—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 67314987HCID 67314987—
ReactantHCID 86229620HCID 86229620—
SolventDiethyl EtherHCID 3283—
SolventIsopropanolHCID 3776—
ProductHCID 67313333HCID 6731333361.9%

Reaction Conditions

Temperature55 °C

Reaction Steps

A mixture of 60 mg (0.25 mmol) of 2-fluoro-5-trifluoromethyl-N-hydroxybenzenecarbox-imidoyl chloride, 50 mg (0.21 mmol) of 3-(3-chlorophenyl) 1-(3-pyridyl)-2-propyn-1-one (prepared similarly to procedures noted above from lithio 3-chlorophenylacetylide and 3-pyridinecarboxaldehyde, followed by IBX oxidation), and 26 mg (0.36 mmol) of sodium bicarbonate in 2.5 mL of isopropyl alcohol was heated at 55° C. overnight with shaking. An additional 30 mg of carboximidoyl chloride and 15 mg of sodium bicarbonate were added, and the reaction was heated for another 24 hrs. The mixture was cooled and diluted with ether. The ether fraction was washed with saturated sodium chloride and dried over magnesium sulfate. The drying agent was filtered off, and solvent was removed by rotoevaporation. The residue was purified by prepTLC to give 56 mg (0.13 mmol) of 5-(3-chlorophenyl)-3-(2-fluoro-5-trifluoromethylphenyl)-4-[(3-pyridyl)carbonyl]isoxazole. 1H NMR (CDCl3): δ 7.10 (t, 1), 7.41 (m, 1), 7.52 (m, 1), 8.65 (br s, 1), and 8.86 ppm (br s, 1). MS m/z: 447.0 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07338967B2
Source datasetuspto-grants-2008_03
ORD IDord-420bf446d4cd41a7b3041f02eca8540c
Source noteuspto-grants-2008_03