HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1958489Generated: October 31, 2026
Ethyl Acetate → Methyl 2-(6-bromo-8-phenylimidazo[1,2-a]pyridin-2-yl)acetate
https://huagongshe.com/reaction/1958489
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Potassium Phosphate, Tribasic | HCID 62657 | — |
| Reactant | Phenylboronic Acid | HCID 66827 | — |
| Reactant | Methyl 2-(6,8-dibromoimidazo[1,2-a]pyridin-2-yl)acetate hydrochloride | HCID 67008341 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | Methyl 2-(6-bromo-8-phenylimidazo[1,2-a]pyridin-2-yl)acetate | HCID 58207940 | 73% |
Reaction Steps
A solution of methyl 2-(6,8-dibromoimidazo[1,2-a]pyridin-2-yl)acetate hydrochloride (0.26 g, 0.68 mmol) and phenylboronic acid (0.083 g, 0.68 mmol) in toluene (9 mL) and ethanol (0.5 mL) was bubbled nitrogen for 20 mins. The mixture was then treated with Pd(PPh3)4 (26 mg, 0.022 mmol) and K3PO4 (2 M, 1 mL, 2.0 mmol) and heated at 80° C. overnight. The reaction was cooled, poured into ethyl acetate (200 mL), washed with brine, separated, and concentrated. The residue was purified by column chromatography on silica gel using ethyl acetate in hexanes (10-25%) as eluent. The product containing fractions were concentrated to give 170 mg (73% yield) of methyl 2-(6-bromo-8-phenylimidazo[1,2-a]pyridin-2-yl)acetate as a white solid. LCMS B: 2.11 min (RT); (M+H)+=347.21 (100%), 345.21 (100%). 1H NMR, 400 MHz, CDCl3: δ 8.20 (d, J=1.6 Hz, 1 H), 7.96 (m, 2 H), 7.65 (s, 1H), 7.50-7.40 (m, 3 H), 7.33 (d, J=1.6 Hz, 1 H), 3.92 (s, 2 H), 3.75 (s, 3 H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08410128B2 |
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| Source dataset | uspto-grants-2013_04 |
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| ORD ID | ord-d5f333a32f1c4fce9ff363804abccb04 |
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| Source note | uspto-grants-2013_04 |
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