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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 895139Generated: November 1, 2026

Bromine → 3-Bromo-7-methylimidazo[1,2-c]pyrimidine

https://huagongshe.com/reaction/895139

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromineHCID 24408—
ReactantSodium AcetateHCID 517045—
ReactantHCID 22385757HCID 22385757—
SolventAcetic AcidHCID 176—
Product3-Bromo-7-methylimidazo[1,2-c]pyrimidineHCID 2238576184.7%

Reaction Steps

To a solution of 7-methylimidazo[1,2-c]pyrimidine (0.3404 g, 2.56 mmol) in acetic acid (10 ml) was added sodium acetate (0.3132 g, 3.82 mmol), then, dropwise over 7 min, a solution of bromine (66.0 μl, 1.28 mmol) in acetic acid (2 ml). The solution was stirred at room temperature for 20 min, then more bromine (19.7 μl, 0.382 mmol) in acetic acid (0.6 ml) was added over 4 min. The solution was stirred at room temperature for a further 15 min, then partitioned between saturated aqueous NaHCO3 (200 ml) and ethyl acetate (200 ml). The aqueous layer (pH 9) was further extracted with ethyl acetate (200 ml), and the combined organic extracts were dried (Na2SO4) and evaporated in vacuo. The residue was purified by flash chromatography (silica gel, EtOAc) to afford 0.2298 g (42%) of the title compound: 1H NMR (360 MHz, CDCl3) δ 2.57 (3H, s), 7.29 (1H, s), 7.56 (1H, s), 8.91 (1H, s); MS (ES+) m/z 212/214 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06914065B2
Source datasetuspto-grants-2005_07
ORD IDord-32b0d6825932486485e2d5d9e264f995
Source noteuspto-grants-2005_07