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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 1,4-Dioxane | HCID 31275 | — |
| Reactant | HCID 86649645 | HCID 86649645 | — |
| Product | N-[(1R)-1-(5-fluoro-2-pyridinyl)ethyl]-3-[(E)-hydroxyiminomethyl]-5-(5-methyl-2-pyridinyl)benzamide | HCID 87195802 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08461185B2 |
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| Source dataset | uspto-grants-2013_06 |
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| ORD ID | ord-a808728829604b97b6336c1d39988188 |
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| Source note | uspto-grants-2013_06 |
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