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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 989387Generated: October 30, 2026

Acetic Acid → HCID 21956403, compound

https://huagongshe.com/reaction/989387

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantAcetonitrileHCID 6342—
ReactantHCID 21956390HCID 21956390—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
ProductHCID 21956403HCID 2195640344%

Reaction Conditions

Temperature-78 °C

Reaction Steps

Acetonitrile (1.3 mL, 24.9 mmol) is added to a −78° C. solution of 9.0 mL of 2.5 M n-butyllithium (22.5 mmol) in 40 mL of tetrahydrofuran. After stirring at −78° C. for 15 min, a solution of 2.86 g (9.02 mmol) of methyl 2-{[(E)-(dimethylamino)methylidene]amino}-6,7-dimethoxy-3-quinolinecarboxylate in 100 mL of tetrahydrofuran is added dropwise over 30 minutes. After stirring at −78° C. for 30 minutes, the reaction mixture is allowed to warm to room temperature and then stirred at room temperature for 1 hour. The reaction mixture is cooled to −78° C. and 3.0 mL of acetic acid is added. The mixture is then stirred at room temperature for 40 min. The solids are collected by filtration washing with water, methanol and ethyl acetate to provide 1.11 g (44%) of 7.8-dimethoxy-4-oxo-1,4-dihydrobenzo[b][1,8]naphthyridine-3-carbonitrile as a light yellow solid, mp>300° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06638929B2
Source datasetuspto-grants-2003_10
ORD IDord-63638d8511ac4b89b00174a2444204d2
Source noteuspto-grants-2003_10