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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 82166Generated: October 25, 2026

Tert-Butylamine → 5-Bromo-N-tert-butyl-2-chloropyrimidin-4-amine

https://huagongshe.com/reaction/82166

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTert-ButylamineHCID 6385—
ReactantTriethylamineHCID 8471—
Reactant5-Bromo-2,4-dichloropyrimidineHCID 289973—
SolventAcetonitrileHCID 6342—
Product5-Bromo-N-tert-butyl-2-chloropyrimidin-4-amineHCID 7907667152%

Reaction Steps

tert-Butylamine (5.28 g, 72 mmol) was added to 5-bromo-2,4-dichloropyrimidine (15 g, 66 mmol) and triethylamine (19.9 g, 197 mmol) in acetonitrile (450 mL) at room temperature and the mixture was stirred at room temperature for 16 hours. Then the mixture was evaporated in vacuo and the crude residue was partitioned between EtOAc (450 mL) and water (400 mL). The organic layer was separated, washed with brine (400 mL) then dried over sodium sulfate and evaporated in vacuo. The residue was purified by column chromatography on silica gel (hexane:EtOAc 88:12) to afford the title compound as a yellow oil in 52% yield, 8.8 g.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08846698B2
Source datasetuspto-grants-2014_09
ORD IDord-1bdd55552f8445d6b076c2c4b1d91528
Source noteuspto-grants-2014_09