HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Cyanophenylboronic acid → 4-(6-Bromoimidazo[1,2-a]pyridin-3-yl)benzonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Cyanophenylboronic acid | HCID 2734326 | — |
| Reactant | 6-Bromo-3-iodoimidazo(1,2-a)pyridine | HCID 22031632 | — |
| Product | 4-(6-Bromoimidazo[1,2-a]pyridin-3-yl)benzonitrile | HCID 89827150 | — |
Reaction Steps
The title compound, light brown solid (0.47 g, 73%), MS (ISP) m/z=298.4 [(M+H)+], mp 176° 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-cyano-phenylboronic acid (0.36 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-02e8038fa04c4acf956542deb2917f28 |
| Source note | uspto-grants-2016_04 |