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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Bromine | HCID 24408 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Reactant | HCID 22385757 | HCID 22385757 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 3-Bromo-7-methylimidazo[1,2-c]pyrimidine | HCID 22385761 | 84.7% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06914065B2 |
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| Source dataset | uspto-grants-2005_07 |
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| ORD ID | ord-32b0d6825932486485e2d5d9e264f995 |
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| Source note | uspto-grants-2005_07 |
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