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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1072313Generated: October 29, 2026

HCID 22391987, compound → HCID 10186267, compound

https://huagongshe.com/reaction/1072313

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 22391987HCID 22391987—
Reactant2-(1-Hydroxy-1-methylethyl)-5-tributylstannylpyridineHCID 22392005—
CatalystPalladium ChlorideHCID 24290—
CatalystFerrocene-1,1'-bis-(diphenylphosphine)HCID 635956—
SolventDimethylformamideHCID 6228—
ProductHCID 10186267HCID 10186267—

Reaction Conditions

Temperature85 °C

Reaction Steps

A mixture of N-cyclopropyl-1-(3,5-dibromophenyl)-1,4-dihydro[1,8]naphthyridin-4-one-3-carboxamide from Step 2, 2-(1-hydroxy-1-methylethyl)-5-tributylstannylpyridine from Step 3 (1.4 eq), 1,1′-bis (diphenylphosphino)ferrocene]dichloropalladium(II) (0.05 eq), and cuprous iodide (0.05 eq) in N,N-dimethylformamide (15 ml/mmol) was stirred at 85° C. for 5 hours. After cooling the resulting mixture was partitioned between ethyl acetate and water. The crude product from the organic phase was chromatographed on silica gel eluting with a 1:6:3 mixture of ethanol, ethyl acetate and methylene chloride to afford the N-Cyclopropyl-1-{5-bromo-3-[6-(1-hydroxy-1-methylethyl)pyridin-3-yl]phenyl}-1,4-dihydro[1,8]naphthyridin-4-one-3-carboxamide compound as a solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06909002B2
Source datasetuspto-grants-2005_06
ORD IDord-21aef699b6b74f77bf8aa079a3ca7f20
Source noteuspto-grants-2005_06