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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 502782Generated: November 4, 2026

Diisopropylethylamine → 5-Bromo-N-methylpyrimidin-2-amine

https://huagongshe.com/reaction/502782

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant5-Bromo-2-chloropyrimidineHCID 606665—
ReactantMethylamine hydrochlorideHCID 6364545—
SolventAcetonitrileHCID 6342—
Product5-Bromo-N-methylpyrimidin-2-amineHCID 13098184—

Reaction Steps

A mixture of 2-chloro-5-bromopyrimidine (2.5 g, 13 mmol), methylamine hydrochloride (7.9 g, 116 mmol), and diisopropylethylamine (18 mL, 103 mmol) in 43 mL acetonitrile was heated in a sealed vessel for 16 h. The reaction was partitioned between EtOAc and water. The organic layer was washed once with brine, dried over anhydrous sodium sulfate, filtered, and concentrated to give 5-bromo-N-methylpyrimidin-2-amine. MS m/z=188 [M+H]+. Calc'd for C5H6BrN3: 187.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07776869B2
Source datasetuspto-grants-2010_08
ORD IDord-abdd6fb2d9cf4f5bb0f6d5b77fbb8481
Source noteuspto-grants-2010_08