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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1635995Generated: October 30, 2026

Pyridine → HCID 73455879, compound

https://huagongshe.com/reaction/1635995

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantHydroxylamine HClHCID 21645—
ReactantHCID 9909644HCID 9909644—
SolventEthanolHCID 702—
ProductHCID 73455879HCID 7345587951.9%

Reaction Conditions

Temperature60 °C

Reaction Steps

800 mg of 3,4-dichloro-N1-{6-[(1-oxo-2,3-dihydro-1H-inden-4-yl)oxy]-3-pyridinyl}benzamide obtained in Example 1 and 670 mg of hydroxyammonium chloride (hydroxylamine hydrochloride) were suspended in 40 ml of ethanol and, after adding 5.4 ml of pyridine to the resulting suspension, the mixture was stirred at 60° C. After 30 minutes, the reaction solution was distilled off under reduced pressure. To the resulting residue, 60 ml of ethyl acetate was added and the solution was washed in turn with water and a saturated sodium chloride solution and then dried over anhydrous magnesium sulfate. After ethyl acetate was distilled off, ether was added to the residue and the deposited crystal was isolated by filtration and then washed with ether to obtain the titled compound (430 mg, white powder).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06511995B1
Source datasetuspto-grants-2003_01
ORD IDord-9597bff40d98439eaec8bd4d0d74c236
Source noteuspto-grants-2003_01