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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1089452Generated: November 1, 2026

2-Aminopyridine → HCID 54716320, compound

https://huagongshe.com/reaction/1089452

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-AminopyridineHCID 10439—
ReactantHCID 85585358HCID 85585358—
SolventTolueneHCID 1140—
ProductHCID 54716320HCID 5471632075.8%

Reaction Steps

A solution of 2.8 g of 2-aminopyridine and 4.2 g of 1,2-dihydro-4-hydroxy-1-phenyl-3-quinolinecarboxylic acid, ethyl ester in 190 ml of toluene was refluxed for 16 hours in a soxhlet apparatus containing 10 g of 4 Å molecular sieves. Evaporation of the volatiles afforded a residue which was purified by means of high pressure liquid chromatography (silica gel: 1:1 ethyl acetate-hexane as the eluent) to yield 3.7 g (73%) of 1,2-dihydro-4-hydroxy-1-phenyl-N-(2-pyridyl)-3-quinolinecarboxamide, m.p. 145° C. (dec).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04966906
Source datasetuspto-grants-1990_10
ORD IDord-e2971b598fcf4ee79a93dc6b8c121e7e
Source noteuspto-grants-1990_10