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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1431311Generated: November 3, 2026

5-Bromo-2-morpholinopyridin-3-amine → N-(5-bromo-2-morpholinopyridin-3-yl)-5,8-difluoro-3-methyl-2-(pyridin-2-yl)quinolin-4-amine

https://huagongshe.com/reaction/1431311

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Bromo-2-morpholinopyridin-3-amineHCID 46737873—
Reactant4-Chloro-5,8-difluoro-3-methyl-2-(pyridin-2-yl)quinolineHCID 59631123—
ProductN-(5-bromo-2-morpholinopyridin-3-yl)-5,8-difluoro-3-methyl-2-(pyridin-2-yl)quinolin-4-amineHCID 59631425—

Reaction Steps

Prepared according to the acid catalyzed Procedure K, Method 2 using 4-chloro-5,8-difluoro-3-methyl-2-(pyridin-2-yl)quinoline (300 mg, 1.03 mmol) and 5-bromo-2-morpholinopyridin-3-amine to give N-(5-bromo-2-morpholinopyridin-3-yl)-5,8-difluoro-3-methyl-2-(pyridin-2-yl)quinolin-4-amine. Mass Spectrum (ESI) m/e=512.0 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08940724B2
Source datasetuspto-grants-2015_01
ORD IDord-352a29a37d0b4eb3bb0637a2899268a8
Source noteuspto-grants-2015_01