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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 553550Generated: October 30, 2026

Phenylboronic Acid → HCID 54740912, compound

https://huagongshe.com/reaction/553550

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenylboronic AcidHCID 66827—
ReactantTributylphenyltinHCID 607632—
ReactantHCID 57742965HCID 57742965—
ReactantHCID 67406545HCID 67406545—
ReactantHCID 67406879HCID 67406879—
CatalystPalladiumHCID 23938—
ProductHCID 54740912HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08048894B2
Source datasetuspto-grants-2011_11
ORD IDord-4bb5091b3f8746e685eb3a07f4581ed1
Source noteuspto-grants-2011_11