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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1710064Generated: October 30, 2026

2-Amino-5-bromopyridine → HCID 54716333, compound

https://huagongshe.com/reaction/1710064

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Amino-5-bromopyridineHCID 70622—
ReactantHCID 85585358HCID 85585358—
SolventTolueneHCID 1140—
ProductHCID 54716333HCID 5471633366%

Reaction Steps

A solution of 21.98 g of 2-amino-5-bromopyridine and 25.0 g of 1,2-dihydro-4-hydroxy-1-phenyl-3-quinolinecarboxylic acid, ethyl ester in 250 ml of toluene was refluxed for 24 hours in a soxhlet apparatus containing 20 g of 4Å molecular sieves. Evaporation of the volatiles afforded a residue which was purified by means of high pressure liquid chromatography (silica gel: dichloromethane as the eluent). The resultant solution was degassed and evaporated to yield 23.56 g (66%) of N-(5-bromo-2-pyridyl)-1,2-dihydro-4-hydroxy-1-phenyl-3-quinolinecarboxamide, m.p. 153°-154° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04952588
Source datasetuspto-grants-1990_08
ORD IDord-245c36da928a41b4a995ba918c72a7f3
Source noteuspto-grants-1990_08