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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1988590Generated: October 27, 2026

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

https://huagongshe.com/reaction/1988590

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 numberUS07642255B2
Source datasetuspto-grants-2010_01
ORD IDord-5eb220b146864183bbccf999ad9efa93
Source noteuspto-grants-2010_01