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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1853187Generated: November 1, 2026

Cyclopentylamine → 5-Bromo-2-chloro-N-cyclopentyl-4-pyrimidinamine

https://huagongshe.com/reaction/1853187

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclopentylamineHCID 2906—
ReactantDiisopropylethylamineHCID 81531—
Reactant5-Bromo-2,4-dichloropyrimidineHCID 289973—
SolventEthanolHCID 702—
Product5-Bromo-2-chloro-N-cyclopentyl-4-pyrimidinamineHCID 4424824789%

Reaction Steps

In a large sealed tube is added 5-bromo-2,4-dichloropyrimidine (3 g, 13.2 mmol) in 100 mL of EtOH. Then cyclopentyl amine (1.95 mL, 19.75 mmol) and N,N′-diisopropylethylamine (3.36 mL, 19.8 mmol) are added to the solution at rt. The solution is then stirred rt overnight. Solvent is evaporated and the crude is purified using silica gel chromatography (15% ethyl acetate/85% hexane) to give (5-bromo-2-chloro-pyrimidin-4-yl)-cyclopentyl-amine as a white solid (3.25 g, 89%). MS (ESI) m/z 278.4 (M+H)+

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08962630B2
Source datasetuspto-grants-2015_02
ORD IDord-e3de2e464fb74995847911ca9dcd74cb
Source noteuspto-grants-2015_02