HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phenylboronic Acid → 6-Bromo-3-phenyl-imidazo[1,2-a]pyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phenylboronic Acid | HCID 66827 | — |
| Reactant | 6-Bromo-3-iodoimidazo(1,2-a)pyridine | HCID 22031632 | — |
| Product | 6-Bromo-3-phenyl-imidazo[1,2-a]pyridine | HCID 52936844 | — |
Reaction Steps
The title compound, off-white solid (0.4 g, 68%), MS (ISP) m/z=273.4 [(M+H)+], mp 77° C., was prepared in accordance with the general method of intermediate E from commercially available 6-bromo-3-iodoimidazo[1,2-a]pyridine (0.7 g, 2.17 mmol) and commercially available phenylboronic acid (0.29 g, 2.38 mmol).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09315502B2 |
| Source dataset | uspto-grants-2016_04 |
| ORD ID | ord-a0021a64a2a4410ba9a3fd75066a4e0e |
| Source note | uspto-grants-2016_04 |