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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2232106Generated: November 1, 2026

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

https://huagongshe.com/reaction/2232106

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 4 Å 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 numberUS04786644
Source datasetuspto-grants-1988_11
ORD IDord-10612abb78df4af8a6949fb8f6b898ee
Source noteuspto-grants-1988_11