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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1866995Generated: November 4, 2026

N-bromobutanimide → 1-[(4-amino-2-methylpyrimidin-5-yl)methyl]-3-bromo-4-hydroxy-6-methylpyridin-2(1H)-one

https://huagongshe.com/reaction/1866995

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
Reactant1-[(4-amino-2-methylpyrimidin-5-yl)methyl]-4-hydroxy-6-methylpyridin-2(1H)-oneHCID 54724214—
SolventAcetic AcidHCID 176—
Product1-[(4-amino-2-methylpyrimidin-5-yl)methyl]-3-bromo-4-hydroxy-6-methylpyridin-2(1H)-oneHCID 5472416672.3%

Reaction Steps

A mixture of 1-[(4-amino-2-methylpyrimidin-5-yl)methyl]-4-hydroxy-6-methylpyridin-2(1H)-one (0.5 g, 0.002 mol), and NBS (0.4 g, 0.002 mol)in glacial acetic acid (5.0 ml) was stirred at room temperature for 1 h under argon atmosphere. Acetic acid was removed in vacuo, residue was triturated with EtOAc containing 10% EtOH, and filtered. The pale yellow precipitate was washed with EtOAc containing 10% EtOH and dried in vacuo to afford the title compound (0.47 g, 725) as a pale yellow powder:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07629363B2
Source datasetuspto-grants-2009_12
ORD IDord-d5d5e4ab67814bb7a156f824cf6f1554
Source noteuspto-grants-2009_12