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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 237588Generated: October 27, 2026

Methyl iodide → 5-bromo-1-methylpyrimidin-2(1H)-one

https://huagongshe.com/reaction/237588

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantPotassium CarbonateHCID 11430—
Reactant5-Bromo-2(1H)-pyrimidinoneHCID 101494—
SolventDimethylformamideHCID 6228—
Product5-bromo-1-methylpyrimidin-2(1H)-oneHCID 139707—

Reaction Steps

A mixture of 5-bromopyrimidin-2(1H)-one (3 g), methyliodide (1.1 mL) and K2CO3 (2.4 g) in N,N-dimethylformamide (60 mL) is stirred for 5 hours at room temperature. The mixture is filtered and the mother liquor is concentrated. The residue is partitioned between water and dichloromethane. The organic phase is washed with brine, dried (MgSO4) and concentrated to give the title compound. Yield: 385 mg; LC (method 9): tR=0.25 min; Mass spectrum (ESI+): m/z=189 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08642585B2
Source datasetuspto-grants-2014_02
ORD IDord-da26afe45c084e588889ca5a8671f02c
Source noteuspto-grants-2014_02