HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phenylboronic Acid → HCID 54740912, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phenylboronic Acid | HCID 66827 | — |
| Reactant | Tributylphenyltin | HCID 607632 | — |
| Reactant | HCID 57742965 | HCID 57742965 | — |
| Reactant | HCID 67406545 | HCID 67406545 | — |
| Reactant | HCID 67406879 | HCID 67406879 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Product | HCID 54740912 | HCID 54740912 | — |
Reaction Steps
Methyl 4-(4-hydroxy-1-methyl-2-oxo-6-phenyl-1,2-dihydroquinolin-3-yl)-4-oxobutanoate. The title compound is prepared by Palladium mediated Suzuki cross coupling reaction of phenyl boronic acid and methyl 4-(4-hydroxy-6-iodo-1-methyl-2-oxo-1,2-dihydro-1,8-naphthyridin-3-yl)-4-oxobutanoate (Method 4) according to the procedure set forth in Miyaura, N.; Suzuki, A. Chem. Rev., 95, 2457-83 (1995). Alternatively, the title compound is prepared by Palladium mediated Stille cross coupling reaction of tributyl(phenyl)stannane and methyl 4-(4-hydroxy-6-iodo-1-methyl-2-oxo-1,2-dihydro-1,8-naphthyridin-3-yl)-4-oxobutanoate according to the procedure set forth in Stille, J. K. Agnew. Chem. Int. Ed. Engl., 25, 508-24 (1986).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08048894B2 |
| Source dataset | uspto-grants-2011_11 |
| ORD ID | ord-4bb5091b3f8746e685eb3a07f4581ed1 |
| Source note | uspto-grants-2011_11 |