Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2222245Generated: October 27, 2026

Methylamine → 5-bromo-2-chloro-N-methylpyrimidin-4-amine

https://huagongshe.com/reaction/2222245

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethylamineHCID 6329—
Reactant5-Bromo-2,4-dichloropyrimidineHCID 289973—
SolventTetrahydrofuranHCID 8028—
Product5-bromo-2-chloro-N-methylpyrimidin-4-amineHCID 1072777175%

Reaction Conditions

Temperature-20 °C

Reaction Steps

5-Bromo-2,4-dichloro-pyrimidine (2.41 g, 10.6 mmol) is slowly treated with methylamine (8 M in EtOH, 3.3 mL) in THF (15 mL) at about −20° C. After stirring for 30 minutes at about −20° C., the reaction mixture is partitioned between CHCl3 and saturated NaHCO3. The aqueous layer is extracted with additional CHCl3 twice and the combined organic layer is dried over MgSO4, filtered and concentrated. The crude product is purified by column chromatography (SiO2, EtOAc/Hexane=3/7) to give 1.76 g (75%) of (5-bromo-2-chloro-pyrimidin-4-yl)-methylamine as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07371750B2
Source datasetuspto-grants-2008_05
ORD IDord-a435d97d10b74d0d93978be0ac94c0f1
Source noteuspto-grants-2008_05