HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Chlorophenylboronic acid → 6-Bromo-3-(4-chlorophenyl)imidazo[1,2-a]pyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Chlorophenylboronic acid | HCID 74299 | — |
| Reactant | 6-Bromo-3-iodoimidazo(1,2-a)pyridine | HCID 22031632 | — |
| Product | 6-Bromo-3-(4-chlorophenyl)imidazo[1,2-a]pyridine | HCID 89826716 | — |
Reaction Steps
The title compound, light yellow solid (0.28 g, 42%), MS (ISP) m/z=307.3 [(M+H)+], mp 157° 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 4-chloro-phenylboronic acid (0.34 g, 2.17 mmol).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09315502B2 |
| Source dataset | uspto-grants-2016_04 |
| ORD ID | ord-5d3491c555bf4797b0fbc54bcd67e821 |
| Source note | uspto-grants-2016_04 |