HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1095669Generated: October 25, 2026
Potassium Carbonate → 8-Bromo-2-(7-(2-methoxyethoxy)imidazo[1,2-a]pyridin-3-yl)quinoline
https://huagongshe.com/reaction/1095669
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1,4-Dioxane | HCID 31275 | — |
| Reactant | 2,8-Dibromoquinoline | HCID 45925951 | — |
| Reactant | 7-(2-Methoxyethoxy)imidazo[1,2-a]pyridine | HCID 58369259 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 8-Bromo-2-(7-(2-methoxyethoxy)imidazo[1,2-a]pyridin-3-yl)quinoline | HCID 66781563 | 72% |
Reaction Steps
A mixture of 2,8-dibromoquinoline (22.4 g, 78.0 mmol), 7-(2-methoxyethoxy)imidazo[1,2-a]pyridine (15.0 g, 78.0 mmol), Pd(PPh3)4 (4.51 g, 3.90 mmol), K2CO3 (21.6 g, 156 mmol) and Pd(OAc)2 (0.876 g, 3.90 mmol), dioxane (312 mL) and water (3 ml) was heated to 100° C. for 18 hours. The resulting mixture was diluted with dichloromethane (500 ml) and filtered. The filtrate was concentrated under reduced pressure and to the resulting oil was added ethyl acetate (100 ml) and methyl tert-butyl ether (100 ml). The resulting mixture was stirred overnight. Filtration to collect the resulting solids yielded the title compound (22.2 g, 72% yield). MS ESI (+) m/z 398 and 400 (M+1 of each isotope) detected.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08138181B2 |
|---|
| Source dataset | uspto-grants-2012_03 |
|---|
| ORD ID | ord-85d9d9830b824c02b2567ddfdce07f9d |
|---|
| Source note | uspto-grants-2012_03 |
|---|