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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2170908Generated: October 30, 2026

3-Aminopyridine → 6-bromo-2-hydroxy-N-(pyridin-3-yl)quinoline-4-carboxamide

https://huagongshe.com/reaction/2170908

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-AminopyridineHCID 10009—
ReactantDiisopropylethylamineHCID 81531—
ReactantPropylphosphonic anhydrideHCID 111923—
ReactantHCID 178524624HCID 178524624—
SolventDichloromethaneHCID 6344—
Product6-bromo-2-hydroxy-N-(pyridin-3-yl)quinoline-4-carboxamideHCID 178522203—

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of 6-bromo-2-hydroxyquinoline-4-carboxylic acid (9.0 g) was dissolved in dichloromethane and cooled to 0° C. 3-aminopyridine (1 eq), T3P (2,4,6-tripropyl-1,3,5,2,4,6-trioxatriphosphinane 2,4,6-trioxide, 50% solution in ethyl acetate, 1.2 eq.), and DIPEA (diisopropylethylamine, 2.0 eq) were added. The solution was stirred at 0° C. for 30 minutes and then allowed to warm to room temperature overnight. The solution was washed with water, sat. sodium chloride, dried, and concentrated. Purification by silica gel column chromatography provided 6-bromo-2-hydroxy-N-(pyridin-3-yl)quinoline-4-carboxamide (9.0 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09051305B2
Source datasetuspto-grants-2015_06
ORD IDord-0cf51df04c2d4bfba6f26599fa057ec2
Source noteuspto-grants-2015_06