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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1467615Generated: November 3, 2026

2-Pyridinecarboxaldehyde → HCID 178519074, compound

https://huagongshe.com/reaction/1467615

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-PyridinecarboxaldehydeHCID 14273—
ReactantSulfuric acid magnesium salt (1:1)HCID 24083—
Reactant4-Amino-1,3-dihydro-2-benzofuran-1-oneHCID 12284649—
SolventDichloromethaneHCID 6344—
ProductHCID 178519074HCID 17851907449.9%

Reaction Steps

4-Aminoisobenzofuran-1(3H)-one (600 mg, 4 mmol), picolinaldehyde (856 mg, 8 mmol) and 1 g of MgSO4 were added into 40 mL of dichloromethane and the mixture was stirred under reflux overnight, then the mixture was evaporated under reduced pressure and the residues was dried in vacuum. 476 mg of (E)-4-(pyridin-2-ylmethyleneamino) isobenzofuran-1(3H)-one was obtained. A mixture of (E)-4-(pyridin-2-ylmethyleneamino) isobenzofuran-1(3H)-one (476 mg, 2 mmol), benzaldehyde (212 mg, 2 mmol), sodium methanolate (432 mg, 8 mmol) and ethyl propionate (40 mL) was stirred at room temperature overnight. Then the resulting mixture was evaporated under reduced pressure and extracted with ethyl acetate (100 mL×4) and concentrated. The crude product was purified by column chromatography (silica gel, petroleum ether: ethyl acetate 20:1 to 5:1) to give 30 mg of methyl 4-oxo-3-phenyl-2-(pyridin-2-yl)-1,2,3,4-tetrahydroquinoline-5-carboxylate; yield 5%. LC-MS (ESI) m/z: 459 (M+1)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08999987B2
Source datasetuspto-grants-2015_04
ORD IDord-36e464cc82a64dd38ac1d39bb4596d9b
Source noteuspto-grants-2015_04