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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1257543Generated: November 2, 2026

Water → N-[(1R)-1-(5-fluoro-2-pyridinyl)ethyl]-3-[(E)-hydroxyiminomethyl]-5-(5-methyl-2-pyridinyl)benzamide

https://huagongshe.com/reaction/1257543

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPyridineHCID 1049—
ReactantAmmonium ChlorideHCID 25517—
Reactant1,4-DioxaneHCID 31275—
ReactantHCID 86649645HCID 86649645—
ProductN-[(1R)-1-(5-fluoro-2-pyridinyl)ethyl]-3-[(E)-hydroxyiminomethyl]-5-(5-methyl-2-pyridinyl)benzamideHCID 87195802—

Reaction Conditions

Temperature70 °C

Reaction Steps

To a solution of N-[(1R)-1-(5-fluoro-2-pyridinyl)ethyl]-3-formyl-5-(5-methyl-2-pyridinyl)benzamide (1.10 g, 3.01 mmol) in dioxane (15 mL) hydroxylamine hydrochloride salt (0.314 g, 4.52 mmol) and pyridine (0.73 mL, 9.04 mmol). The reaction mixture was stirred at 70° C. for 18 h. The mixture was cooled to ambient temperature. Saturated aqueous ammonium chloride and water were added. The mixture was extracted with dichloromethane (3×). The combined organic extracts were washed with brine, dried over magnesium sulfate, filtered and concentrated. Purification by silica gel chromatography (95% dichloromethane/methanol→85% dichloromethane/methanol) gave the title compound (0.91 g). MS 379.1 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08461185B2
Source datasetuspto-grants-2013_06
ORD IDord-a808728829604b97b6336c1d39988188
Source noteuspto-grants-2013_06