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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 727093Generated: October 31, 2026

Water → HCID 798732, compound

https://huagongshe.com/reaction/727093

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium hydrideHCID 24758—
ReactantN'-HydroxybenzenecarboximidamideHCID 69186—
Reactant3-methylpyridine-4-carboxamideHCID 2762489—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
ProductHCID 798732HCID 79873225.2%

Reaction Conditions

Temperature50 °C

Reaction Steps

To a mixture of benzamide oxime (12.8 g, 94 mmol) and 4 Å sieves (80 g) in tetrahydrofuran (250 ml) under a nitrogen atmosphere was carefully added sodium hydride (55% dispersed in oil, 4.3 g, 98 mmol) portionwise. When addition was complete the reaction was heated at 50° C. for 1 hour. Methyl isonicotinamide (5.6 ml, 47 mmol) in tetrahydrofuran (50 ml) was added, and the reaction stirred at reflux for 2 hours. The reaction was cooled to room temperature and water (200 ml) and dichloromethane (300 ml) added. The mixture was filtered through a pad of Celite and the two phases separated. The aqueous phase was extracted with a further portion of dichloromethane (250 ml). The combined organic phases were washed with saturated brine (200 ml), dried (MgSO4) and evaporated in vacuo. The residue was triturated with ethyl acetate to yield the title compound as a white solid (2.64 g, 25%). δH (CDCl3) 7.50-7.56 (3H, m, ArH), 8.05-8.07 (2H, m, ArH), 8.16-8.19 (2H, m, ArH), 8.89 (2H, dd, J 4.4, 1.6 Hz, pyridyl 2-H, 6-H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05712285
Source datasetuspto-grants-1998_01
ORD IDord-ca57ee9035b54a87aeaaf53d0d0c571f
Source noteuspto-grants-1998_01