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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 901233Generated: October 27, 2026

Phosphorus oxychloride → 1-Benzyl-4-chloro-2-oxo-1,2-dihydro-[1,8]-naphthyridine-3-carbonitrile

https://huagongshe.com/reaction/901233

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosphorus oxychlorideHCID 24813—
Reactant1-Benzyl-4-hydroxy-2-oxo-1,2-dihydro-[1,8]-naphthyridine-3-carboxylic Acid CyclohexylamideHCID 59699565—
Product1-Benzyl-4-chloro-2-oxo-1,2-dihydro-[1,8]-naphthyridine-3-carbonitrileHCID 5969954952%

Reaction Steps

A solution of 1-benzyl-4-hydroxy-2-oxo-1,2-dihydro-[1,8]-naphthyridine-3-carboxylic acid cyclohexylamide (7) (1.3 g, 3.44 mmol) in neat POCl3 was heated overnight at 90° C. The solution was cooled and the excess POCl3 was distilled under vacuum. The residue was suspended in water, basified by saturated NaHCO3 solution and extracted by dichloromethane. The combined organic phase washed subsequently by a saturated NaHCO3 solution, water and brine, dried over Na2SO4, and evaporated. The residue was crystallized by acetone to yield 530 mg (52%) of 1-benzyl-4-chloro-2-oxo-1,2-dihydro-[1,8]-naphthyridine-3-carbonitrile (8) as white solids. MP: 188° C.; 1H-NMR (DMSO-d6): δ 5.61 (s, 2H), 7.21-7.31 (m, 5H), 7.56 (dd, J=4.8, 8.0 Hz, 1H), 8.53 (dd, J=1.6, 8.0 Hz, 1H), 8.86 (dd, J=1.6, 8.0 Hz, 1H); EIMS: 296 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07361760B2
Source datasetuspto-grants-2008_04
ORD IDord-fcbd1119d09c4b9d91b9ed443cd4f2ac
Source noteuspto-grants-2008_04