HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Fluorophenylboronic acid → HCID 71259057, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Fluorophenylboronic acid | HCID 2734354 | — |
| Reactant | HCID 19828469 | HCID 19828469 | — |
| Product | HCID 71259057 | HCID 71259057 | — |
Reaction Steps
Subsequently, Suzuki-Miyaura conditions were applied as in FIG. 8 using 2-bromo-5,6,7,8-tetrahydroquinoline and 2-fluorophenylboronic acid to obtain the 2-(2-fluorophenyl)-5,6,7,8-tetrahydroquinoline precursor as depicted in FIG. 10. After isolation and purification by flash chromatography, this viscous yellow-orange liquid solidifies at room temperature. In general, 2-(2-fluorophenyl)-pyridine derivatives wore prepared in high yields (over 92%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09040704B2 |
| Source dataset | uspto-grants-2015_05 |
| ORD ID | ord-6a1677c9eb3a4fa7a26e5118624e0007 |
| Source note | uspto-grants-2015_05 |