HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phenylboronic Acid → HCID 86732155, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phenylboronic Acid | HCID 66827 | — |
| Reactant | HCID 86732156 | HCID 86732156 | — |
| Product | HCID 86732155 | HCID 86732155 | — |
Reaction Steps
The title compound was synthesized by procedures and steps analogous to those described in Method O, Example 111, but using phenylboronic acid and (4S,6S)-4-(5-((4-chloropyridin-2-yl)amino)-2-fluorophenyl)-4-(fluoromethyl)-6-(trifluoromethyl)-5,6-dihydro-4H-1,3-oxazin-2-amine (Example 16) as coupling partners. MS m/z=463 [M+H]+. Calculated for C23H19F5N4O: 462.4.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09296734B2 |
| Source dataset | uspto-grants-2016_03 |
| ORD ID | ord-408fc468e0054f49a3e41e2b1135b5c8 |
| Source note | uspto-grants-2016_03 |